The inventions disclosed herein pertain to breast imaging using tomosynthesis, and more specifically to a system and method for guiding the navigation of a tomosynthesis data set, which employs a synthesized 2D image that is obtained by importing relevant data from the tomosynthesis data set into the synthesized image, and then using the 2D image to navigate the tomosynthesis data.
Mammography has long been used to screen for breast cancer and other abnormalities. Traditionally, mammograms have been formed on x-ray film. More recently, flat panel digital imagers have been introduced that acquire a mammogram in digital form, and thereby facilitate analysis and storage of the acquired images, and provide other benefits as well. Further, substantial attention and technological development has been dedicated towards obtaining three-dimensional images of the breast, using methods such as breast tomosynthesis. In contrast to the 217 images generated by legacy mammography systems, breast tomosynthesis systems construct a 3D image volume from a series of 2D projection images, each projection image obtained at a different angular displacement of an x-ray source relative to the image detector as the x-ray source is scanned over the detector. The constructed 3D image volume is typically presented as a plurality of slices of image data, the slices being geometrically reconstructed on planes parallel to the imaging detector. The reconstructed tomosynthesis slices reduce or eliminate the problems caused by tissue overlap and structure noise present in single slice, two-dimensional mammography imaging, by permitting a medical professional (e.g., a radiologist) to scroll through the image slices to view underlying structures.
Tomosynthesis systems have recently been developed for breast cancer screening and diagnosis. In particular, Hologic, Inc. (www.hologic.com), has developed a fused, multimode mammography/tomosynthesis system that acquires one or both types of mammogram and tomosynthesis images, either while the breast remains immobilized or in different compressions of the breast. Other companies have proposed the introduction of systems which are dedicated to tomosynthesis imaging; i.e., which do not include the ability to also acquire a mammogram.
However, systems restricted to tomosynthesis acquisition and image display may present an obstacle to acceptance of the tomosynthesis imaging technology, as medical professionals have grown accustomed to screening and analysis of conventional 2D mammogram images. In particular, mammograms provide good visualization of micro-calcifications, and can offer higher spatial resolution when compared with tomosynthesis images. While tomosynthesis images provided by dedicated breast tomosynthesis systems have other desirable characteristics, e.g., better isolation and visualization of structures in the breast, such systems do not leverage the existing interpretation expertise of medical professionals.
Examples of systems and methods that leverage existing medical expertise in order to facilitate the transition to tomosynthesis technology are described in U.S. Pat. No. 7,760,924, which is hereby incorporated by reference in its entirety. In particular, U.S. Pat. No. 7,760,924 describes a method of generating a synthesized 2D image, which may be displayed along with tomosynthesis projection or reconstructed images, in order to assist in screening and diagnosis.
According to one aspect of the inventions disclosed and described herein, a system and method for processing, displaying and navigating breast tissue information is provided, wherein the system is configured for, and the method includes: (i) obtaining a plurality of 2D and/or 3D images of a patient's breast; (ii) generating a synthesized 2D image of the patient's breast from the obtained 2D and/or 3D images of the plurality; (iii) displaying the synthesized 2D image; (iv) receiving a user command, or otherwise detecting through a user interface, a user selection or other indication of an object or region in the synthesized 2D image; and (v) displaying at least a portion of one or more images from the plurality, including a source image and/or most similar representation of the user selected or indicated object or region.
Additionally and/or alternatively, the system may be configured for, and the method may include, concurrently displaying a respective source image and/or most similar representation of a tissue structure or region that corresponds to a given location of a user movable input device in the displayed synthesized 2D image. While various image processing techniques may be employed for providing the this navigational functionality, in a preferred embodiment, the system is preferably configured for, and the method further includes, generating an index map comprising identifying information of selected images of the plurality of 2D and/or 3D images that are source images or that otherwise contain a most similar representation of regions and/or objects displayed in the synthesized 2D image. The index map can thereafter be used by the system for to greatly reduce the time needed to navigate through the images, e.g., a tomosynthesis volume stack of the breast image volume.
The plurality of source images may include one or more of tomosynthesis projection images, reconstructed tomosynthesis slices, mammograms, contrast enhanced mammograms, and synthesized two dimensional images. In various embodiments, the plurality of 2D and/or 3D images of a patient's breast are acquired or synthesized X,Y coordinate slices at differing z axis locations of the breast, the images having one or more corresponding X,Y coordinate locations. In one embodiment, generating the synthesized 2D image includes constructing a merged image by importing one or more objects and/or regions from the images of the plurality into the merged image, wherein an image from which an object or region is imported into the merged image comprises a source image for that object or region. In such embodiment, objects or regions are preferably imported into the merged image at X,Y coordinate locations corresponding to the X,Y coordinate locations of the respective objects or regions in their source image. Further to such embodiment, each image of the plurality of 2D and/or 3D images preferably contains one or more regions defined by their X,Y coordinate locations that are common for all images of the plurality, wherein one of each said common region is imported from the plurality of images into the merged image based upon a comparison of one or more system and/or user defined attributes of the respective common region of each image.
In a preferred variation of this embodiment, an identified object or region of interest in a given image has priority for importation into the merged image over any other identified objects or regions of interest having the same or overlapping X,Y coordinate locations in other image slices based upon a predefined priority scheme, e.g., to reflect the relative clinical importance of the various possible tissue structures. The preferred attributes may include attributes indicative of regions of interest, such as cancers, or alternatively such as more accurate representation of breast density or breast anatomy, i.e., truthful breast-border/nipple appearance, or presence of a contrast agent in the case of contrast enhanced mammography. In general, any attribute capable to delivering a high/better-quality image can be relevant.
In various embodiments, an object or region may be automatically highlighted in the synthesized 2D image and/or displayed at least portion of the one or more images from the plurality. Additionally and/or alternatively, an object or region in the synthesized 2D image and/or displayed at least portion of the one or more images from the plurality may be highlighted in response to a further received user command or to certain user activity detected through the user interface. By way of non-limiting example, an object or region may is highlighted by a contour line representing a boundary of the highlighted object or region. Preferably, the object or region is highlighted in a manner indicating that the highlighted object or region is or contains a specified type of tissue structure.
According to another aspect of the inventions disclosed and described herein, a system and method for processing, displaying and navigating breast tissue information is provided, wherein the system is configured for, and the method includes: (i) obtaining a plurality of tomosynthesis images comprising volumetric image data of a patient's breast; (ii) generating a synthesized 2D image of the patient's breast at least in part from the tomosynthesis images; (iii) displaying the synthesized 2D image; (iv) receiving a user command, or otherwise detecting through a user interface, a user selection or other indication of an object or region in the synthesized 2D image; and (v) displaying at least a portion of one or more tomosynthesis images from the plurality, including a source image and/or most similar representation of the user selected or indicated object or region. Again, while various image processing techniques may be employed for providing the this navigational functionality, in a preferred embodiment, the system is preferably configured for, and the method further includes, generating an index map that includes identifying information of selected tomosynthesis images of the plurality that are source images or that otherwise contain a most similar representation of regions and/or objects in the synthesized 2D image.
These and other aspects and embodiments of the disclosed inventions are described in more detail below, in conjunction with the accompanying figures.
In describing the depicted embodiments of the disclosed inventions illustrated in the accompanying figures, specific terminology is employed for the sake of clarity and ease of description. However, the disclosure of this patent specification is not intended to be limited to the specific terminology so selected, and it is to be understood that each specific element includes all technical equivalents that operate in a similar manner. It is to be further understood that the various elements and/or features of different illustrative embodiments may be combined with each other and/or substituted for each other wherever possible within the scope of this disclosure and the appended claims.
The following abbreviations shall have the following definitions throughout this patent specification:
Mp refers to a conventional mammogram or contrast enhanced mammogram, which are two-dimensional (2D) projection images of a breast, and encompasses both a digital image as acquired by a flat panel detector or another imaging device, and the image after conventional processing to prepare it for display and/or storage or other use.
Tp refers to an image that is similarly two-dimensional (2D), but is acquired at a respective tomosynthesis angle between the breast and the origin of the imaging x rays (typically the focal spot of an x-ray tube), and encompasses the image as acquired, as well as the image data after being processed for display and/or storage or other use.
Tr refers to an image that is reconstructed from tomosynthesis projection images Tp, for example, in the manner described in one or more of U.S. Patent Application Publication No. 2010/0135558, and U.S. Pat. Nos. 7,760,924, 7,606,801, and 7,577,282, the disclosures of which are fully incorporated by reference herein in their entirety, wherein a Tr image represents a slice of the breast as it would appear in a projection x ray image of that slice at any desired angle, not only at an angle used for acquiring Tp or Mp images.
Ms refers to synthesized 2D images, which simulate mammography images, such as a craniocaudal (CC) or mediolateral oblique (MLO) images, and are constructed using tomosynthesis projection images Tp, tomosynthesis reconstructed images Tr, or a combination thereof. Examples of methods that may be used to generate Ms images are described in the above-incorporated U.S. Patent Application Publication No. 2010/0135558, and U.S. Pat. No. 7,760,924.
IMERGE refers to a 2D image constructed by importing into a single image one or more objects and/or regions from any two or more of Mp, Ms, Tp or Tr images of a patient's breast, wherein an image from which an object or region is imported into the merged image comprises a source image for that object or region, and wherein objects or regions are imported into the merged image at X,Y coordinate locations corresponding to the X,Y coordinate locations of the objects or regions in their respective source image
The terms IMERGE, Tp, Tr, Ms and Mp each encompasses information, in whatever form, that is sufficient to describe the respective image for display, further processing, or storage. The respective IMERGE, Mp, Ms. Tp and Tr images are typically provided in digital form prior to being displayed, with each image being defined by information that identifies the properties of each pixel in a two-dimensional array of pixels. The pixel values typically relate to respective measured, estimated, or computed responses to x rays of corresponding volumes in the breast, i.e., voxels or columns of tissue. In a preferred embodiment, the geometry of the tomosynthesis images (Tr and Tp), mammography images (Ms and Mp) and the merged image IMERGE are matched to a common coordinate system, as described in U.S. Pat. No. 7,702,142, the disclosure of which is hereby incorporated by reference in its entirety. Unless otherwise specified, such coordinate system matching is assumed to be implemented with respect to the embodiments described in the ensuing detailed description of this patent specification.
More particularly, the image generation and display system includes an image acquisition system 1 that acquires tomosynthesis image data for generating Tp images of a patient's breasts, using the respective three dimensional and/or tomosynthesis acquisition methods of any of the currently available systems. If the acquisition system is a combined tomosynthesis/mammography system, Mp images may also be generated. Some dedicated tomosynthesis systems or combined tomosynthesis/mammography systems may be adapted to accept and store legacy mammogram images, (indicated by a dashed line and legend Mplegacy in
The Tp images are transmitted from either the acquisition system 1, or from the storage device 2, or both, to a computer system configured as a reconstruction engine 3 that reconstructs the Tp images into reconstructed image “slabs” Tr, representing breast slices of selected thickness and at selected orientations, as disclosed in the above-incorporated patents and application publication. The imaging and display system 1 further includes a 2D synthesizer that operates substantially in parallel with the reconstruction engine for generating 2D images that simulate mammograms taken at any orientation (e.g., CC or MLO) using a combination of one or more Tp and/or Tr images. The synthesized 2D images may be generated dynamically prior to display (as shown in
Mode filters 7a, 7b are disposed between image acquisition and image display. Each of the filters 7a and 7b may additionally include customized filters for each type of image (i.e., Tp, Mp, Tr) arranged to identify and highlight certain aspects of the respective image types. In this manner, each imaging mode can be tuned or configured in an optimal way for a specific purpose. The tuning or configuration may be automatic, based on the type of the image, or may be defined by manual input, for example through a user interface coupled to a display. In the illustrated embodiment of
According to one aspect of the disclosed inventions, and as described in greater detail herein, the system 1 includes an image merge processor 6 that merges relevant image data obtained from a set of available source and synthesized images of a patient's breast to provide a merged 2D image IMERGE for display. The set of available images used to generate the merged image IMERGE may include filtered and/or unfiltered Ms, Mp, Tr and/or Tp images. While
By way of illustration, a medical professional, such as a radiologist, may wish to merge two or more reconstructed tomosynthesis slices (or slabs) in order to provide a merged image showing the most readily discerned structures in the collective tomosynthesis image data in a displayed synthesized 2D image, which essentially maps the tomosynthesis slices (or slabs) at a pixel wise granularity. Additionally or alternatively, the radiologist may combine a 2D mammogram image, whether Mp or Ms, with a 3D projection, or with selected reconstructed images, in order to obtain a customized merged image that highlights both calcifications and various tissue structures in the breast. Filters applied to each type of image can further highlight the types of structures or features in the merged image that are generally most prevalent or most readily discerned in the respective source image type. Thus, one type of filter may be applied to mammography images to highlight calcifications, while a different filter may be applied to tomosynthesis slices to highlight masses, allowing both the highlighted calcifications and highlighted tissue masses to be displayed in the single merged image. Filters may also provide the merged image with a desired look and feel; i.e., to make the merged image appear more like a tomosynthesis or mammography image.
The display system 5 may be part of a standard acquisition workstation (e.g., of acquisition system 1), or of a standard (multi-display) review station that is physically remote from the acquisition system 1. In some embodiments, a display connected via a communication network may be used, for example, a display of a personal computer or of a so-called tablet, smart phone or other hand-held device. In any event, the display 5 of the system is preferably able to display IMERGE, Ms, Mp and Tr (and/or Tp) images concurrently, e.g., in separate side-by-side monitors of a review workstation, although the invention may still be implemented with a single display monitor, by toggling between images.
To facilitate the detection/diagnosis process, Tr slices are preferably reconstructed all to the same size for display, which can be the same as the size of an Mp or Ms image of the breast, or they can be initially reconstructed to sizes determined by the fan shape of the x ray beam used in the acquisition, and then later converted to that same size by appropriate interpolation and/or extrapolation. In this manner, images of different types and from different sources can be displayed in desirable size and resolution. For example, an image can be displayed in (1) Fit To View Port mode, in which the size of the displayed image size is maximized such that the entire imaged breast tissue is visible, (2) True Size mode, in which a display pixel on the screen corresponds to a pixel of the image, or (3) Right Size mode, in which the size of a displayed image is adjusted so that it matches that of another image being concurrently displayed, or with which the displayed image is, or can be, toggled.
For example, if two images of the same breast are taken and are not the same size, or do not have the same resolution, provisions may be made to automatically or user-selectively increase or reduce the magnification (i.e., “zoom in” or “zoom out”) of one or both images, such that they appear to be the same size when they are concurrently displayed, or as a user toggles between the images. Known interpolation, extrapolation and/or weighting techniques can be used to accomplish the re-sizing process, and known image processing technology can also be used to make other characteristics of the displayed images similar in a way that facilitates detection/diagnosis. When viewing such resized images, according to one embodiment of the disclosed inventions, the merged image IMERGE is automatically resized, accordingly.
Thus, the system 1, which is described as for purposes of illustration and not limitation in this patent specification, is capable of receiving and displaying selectively tomosynthesis projection images Tp, tomosynthesis reconstruction images Tr, a synthesized mammogram image Ms, and/or mammogram (including contrast mammogram) images Mp, or any one or sub combination of these image types. The system 1 employs software to convert (i.e., reconstruct) tomosynthesis images Tp into images Tr, software for synthesizing mammogram images Ms, and software for merging a set of images to provide a merged image that displays, for every region of the merged image, the most relevant feature in that region among all images in the source image set. For the purpose of this patent specification, an object of interest or feature in a source image may be considered a ‘most relevant’ feature for inclusion in the merged image based upon the application of one or more CAD algorithms to the collective source images, wherein the CAD algorithms assign numerical values, weights or thresholds, to pixels or regions of the respective source images based upon identified/detected objects and features of interest within the respective region or between features or, in instances when the merged image is generated directly from the synthesized image without CAD assistance, simply the pixel value, weight or other threshold associated with a pixel or region of the image. The objects and features of interest may include, for example, spiculated lesions, calcifications, and the like. Various systems and methods are currently well known for computerized detection of abnormalities in radiographic images, such as those disclosed by Giger et al. in RadioGraphics, May 1993, pp. 647-656; Giger et al. in Proceedings of SPIE, Vol. 1445 (1991), pp. 101-103; U.S. Pat. Nos. 4,907,156, 5,133,020, 5,343,390, and 5,491,627, each of which being hereby incorporated by reference in its entirety.
As discussed above, the image with the most desirable display data may be an image with a highest pixel value, a lowest pixel value, or which has been assigned a threshold value or weight based on the application of a CAD algorithm to the image. When the image with the most desirable display data for that region is identified, the pixels of that region are copied over to the corresponding region of the merged image. For example, as shown in
Once the merged image is generated, it may be used to assist in the navigation through a tomosynthesis image data stack from which the merge image was generated. Such navigation is a two-step process comprising selection of various objects of interest, and display of corresponding tomosynthesis images that are the source of such objects of interest in the merged image. By way of example,
The presently disclosed inventions envision many different mechanisms for selection of the objects of interest and corresponding display of the respective source images corresponding; although it is to be understood that the disclosed inventions are not limited to those described herein. For example, the selection of a region or area within the merged image may include a selection of a CAD mark, or alternatively a selection of a particular feature of interest to the reviewer. Although in both instances the most relevant slices are made available to the user, the mechanics behind the processes differ. One such preferred mechanism is illustrated in
Selection Using CAD Marks:
In addition or alternatively to use of a merge/guidance map, if the merged image is presented with a CAD overlay, the CAD overlay may include either CAD marks derived from 3D data, or CAD marks derived from 2D data (if the system has the ability to obtain 2D data). CAD marks derived from 3D data generally include, as part of the data object associated with the mark, identifiers of one or more slices which contributed to the generation of the 3D mark. When the merged image is overlaid with 3D CAD data, selection of the CAD mark results in the retrieval of the series of slices that contributed to the mark. In one embodiment, the central image slice is displayed; in alternate embodiments, the image slice having the highest weight is displayed; and in a still further alternate embodiment, the image slice having the least visual noise (i.e., the clearest image) is displayed.
Selection by Objects of Interest:
As an alternate to selecting by CAD marks, a mechanism is provided for allowing a user to select any object on a merged image, whether it is a CAD mark, or a feature of interest, such as any abnormality or irregularity in the image. In one embodiment, the user or system may select a region, using for example a mouse click for a single pixel area, or a click and drag action to select a larger region. Alternatively, the user may be provided with a selection of graphical frames of various or variable sizes, and have the ability to move the frame to different locations within the merged image to select areas when it is desired to view additional tomosynthesis image slices. In response to such a selection, the particular image slice for initial display may be selected in a variety of ways.
For example, an image slice could be selected based on the weighting of its associated pixel within the selected region. Or a particular image slice may be selected because a particular feature which is selected, or which is near a pixel or region that is selected, is best viewed in the selected image slice, e.g., provides the clearest view of that region. Thus, the identification of a particular image slice that is most relevant to a selected pixel or region may utilize pixel information that surrounds the selected object, for example, using region growing techniques known to those in the art. Thus, pixels that neighbor the selected pixel or region are included in the evaluation for relevant slices if the pixels have a characteristic that satisfies a certain threshold established by the user; for example, including but not limited to the pixels having a particular weight, or being arranged in a particular pattern, etc.
Alternatively, a group of image slices may be selected, e.g., a successive order of image slices, with a central slice or most heavily weighted slice being first presented. As described above, alternatively the image slice within the group having the least noise, i.e., the clearest slice, may be provided. In addition, the selection of an image slice for presentation may also take into account a desired visualization mode. Thus, if the user-specified purpose is to visualize calcifications, an image slice having calcification features may be presented ahead of another slice within the group having a lesser calcification characteristic.
It will be appreciated that the disclosed and described systems and methods in this patent specification are designed to condense the image information made available from a tomosynthesis reconstruction volume (or “stack”) containing a patient's 3D breast image data down to a single, synthesized 2D image, similar to a conventional 2D mammographic image. By reviewing this synthesized 2D image concurrently with the 3D tomosynthesis stack, it is possible to provide a much more efficient and accurate review of the patient's breast tissue. This is because the synthesized 2D merged image can act as a guidance-map, so that the medical professional reviewing the images can focus on the synthesized 2D image for detecting any objects or regions of interest that merit further review, and the system can provide immediate, automated navigation to a “best” corresponding tomosynthesis image slice (or a subset of adjacent tomosynthesis slices) to allow the medical professional to conduct this further review, verify and evaluate the finding. Thus, it is preferred, although not required for practicing all embodiments of the disclosed inventions, for the medical professional to employ a user interface that can display a respective synthesized 2D merged image along-side the tomosynthesis volume image slices, for concurrent viewing of both.
The synthesized 2D image is displayed to the medical professional (interchangeably referred to as the “user” of the described system), typically on a workstation having side-by-side monitors as depicted in
Thereafter, the medical professional (user) may use the user-interface to activate the navigational capability of the system. In particular, at step 94, the user may affirmatively input a command to select a particular object or region in the displayed synthesized 2D image. Alternatively, the system may be configured so that the user merely positions a “pointer,” e.g., a movable cross or arrowhead that is controlled using a mouse or similar input device), overlying an object or region in the displayed synthesized 2D image, thereby “indicating” an interest in the item. In response to the received command or indication, using the index map, the system may easily retrieve, at step 96, and display on the right-hand-side monitor, at step 98, the tomosynthesis slice that is either the direct source of the user selected/indicated object or region, or which otherwise contains a most similar representation of the object or region as depicted in the displayed 2D image. Additionally and/or alternatively, the system may be configured for concurrently displaying a respective source image and/or most similar representation of a tissue structure or region that corresponds to a given location of a user movable input device in the displayed synthesized 2D image.
The plurality of 2D and/or 3D images from which a synthesized 2D image is generated may include tomosynthesis projection images, tomosynthesis reconstruction slices, mammography images, contrast enhanced mammography images, synthesized 2D images, and combinations thereof. It will be appreciated that the synthesized 2D image advantageously incorporates the most relevant information from each of the underlying acquired and computer generated image data sets of the patient's breast. Thus, different regions of pixels in the displayed synthesized 2D image may be sourced from corresponding different images in the underlying image data set, depending on which underlying image is best for viewing an object of interest, e.g., a mass or a calcification, in the respective region. The particular regions may be identified statically, i.e., within a particular grid, or dynamically, i.e., based on identified objects of interest, and may range in granularity from as little as one pixel, to all pixels in the respective image. In one embodiment, priority is given to first importing into a merged image under construction those regions containing one or more specific tissue structures of interest in the images of a tomosynthesis image data set (or “stack”), and thereafter populating the remaining regions of the merged image with the otherwise most relevant regions from the images, as described above.
The user interface may additionally include features to enable the medical professional to manipulate the presented tomosynthesis data, for example, to allow the medical professional to scan through adjacent image slices of the tomosynthesis stack, or to further zoom (magnify) into a selected region, to place markers, or alternatively to apply filters or other image processing techniques to the image data. In this manner, the medical professional may quickly review a large stack of tomosynthesis data by utilizing a synthesized 2D image for navigation purposes, thereby increasing the performance and efficiency of breast cancer screening and diagnosis. According to a further aspect of the disclosed inventions, it has been determined or otherwise appreciated that particular types of images may include or be superior for viewing different types of relevant information. For example, calcifications are typically best visualized in 2D mammograms, while masses are typically best visualized using 3D reconstructed images.
Thus, in one embodiment of the disclosed inventions, different filters are applied to each of the different types of underlying 2D and/or 3D images in the image data set used to generate the merged image, the filters selected to highlight particular characteristics of the images that are best displayed in the respective imaging mode. Appropriate filtering of the images prior to generating the merged image helps ensure that the final merged image includes the most relevant information that can be obtained from all the underlying image types. Additionally and/or alternatively, the type of filtering performed for the various images may be defined via user input, which permits a user to select a ‘merge mode’, for example, geared towards highlighting masses, calcifications, or for making the merged image appear to be a particular image type, such as a 3D reconstructed slice, or a 2D mammogram.
Synthesizing the 2D image may be accomplished in a variety of ways. For example, in one embodiment, general purpose image filtering algorithms are used to identify features within each of the respective 2D and 3D images, and a user may select whether to use 2D filtered data or 3D filtered data to generate the merged image. Alternatively, 2D or 3D filtered data may be automatically selected in accordance with a particular visualization mode that has been user selected; for example, 2D filtered data may be automatically selected by the system for calcification visualization mode, while 3D filtered data may be automatically selected by the system for mass visualization modes. In one embodiment, two different merged images may be constructed, one for each mode; alternatively, a single merged image may be constructed that takes into account the respective filtered image data results from all available image types.
In one embodiment, features (representing potential objects of interest) are identified in the available source images and thereafter weighted, e.g., on a pixel by pixel or region by region basis in each respective image. A 2D image is then constructed by incorporating the respective regions having the most significant weight in individual images of the available source images. The size of the region may vary in granularity from one pixel to many (or even all) pixels of the respective image, and may be statically pre-defined, or may have margins that vary in accordance with the varying thresholds of the source images. The synthesized (aka “merged”) image may be pre-processed and stored as a DICOM object following tomosynthesis acquisition, and thereafter forwarded with the reconstruction data for subsequent review by a medical professional. Such an arrangement removes the need to forward weighting information for each reconstructed slice. Alternatively, the stored DICOM object may include the weighting information, allowing the merged image to be dynamically constructed in response to a request for a synthesized 2D image at the medical professional's work station. In one embodiment, both the weighting information and the synthesized 2D image may be provided in the DICOM object, allowing presentation of a default merged image, while still enabling customization according to the personal workflow of the reviewer. To be clear, the weighting information can be stored with the image itself, and need not be a separate file.
It is realized that the visualization of the synthesized 2D images may have some drawbacks. For example, there may be neighboring regions in the merged image which exhibit bright calcifications, but which in fact are sourced from image slices that are distant from one another in the z plane. Therefore, what may appear to be a cluster of micro-calcifications in the 2D image may, in fact, be individual calcifications that are distributed (i.e., along the z-axis) throughout the breast and thus do not actually represent a micro-calcification cluster that requires further review. Thus, according to a further aspect of the disclosed inventions, a ‘cluster spread indicator’ may be provided with the synthesized 2D image, which visually indicates the distribution of calcifications along the z-plane, allowing the medical professional to quickly assess whether a group of calcifications comprise a calcification cluster.
In some instances, the system may determine based on the index map information that more than one tomosynthesis image slice should be displayed for a selected/indicated object type or region, for example, a spiculated mass. In such instances, a series of two or more adjacent tomosynthesis slices are displayed, one after the other, at a timing interval that is preferably user selected. As will be additionally described herein, the user may select or indicate more than one object or region in a given synthesized 2D image. Once the user has completed his or her review of the displayed tomosynthesis slice(s), the process is complete (at step 100) for the particular breast image data.
As previously pointed out, while various image processing techniques may be employed for providing the this navigational functionality, in a preferred embodiment, the system is preferably configured for, and the method further includes, generating an index map comprising identifying information of selected images of the plurality of 2D and/or 3D images that are source images or that otherwise contain a most similar representation of regions and/or objects displayed in the synthesized 2D image. The index map can thereafter be used by the system for to greatly reduce the time needed to navigate through the images, e.g., a tomosynthesis volume stack of the breast image volume.
An implementation of one preferred process 102 for generating an index map will now be described in conjunction with the flow diagram shown in
However, in parallel with the creation of the generic index map 108, an object type index map 114 is generated, in which individual object types, designated as 110-1 to 110-n in
As noted above, in various embodiments, an object or region may be automatically highlighted in the synthesized 2D image and/or displayed at least portion of the one or more images from the plurality. Additionally and/or alternatively, an object or region in the synthesized 2D image and/or displayed at least portion of the one or more images from the plurality may be highlighted in response to a further received user command or to certain user activity detected through the user interface. By way of non-limiting example, an object or region may is highlighted by a contour line representing a boundary of the highlighted object or region. Preferably, the object or region is highlighted in a manner indicating that the highlighted object or region is or contains a specified type of tissue structure.
By way of illustration,
It should be appreciated that there will be instances in which the mapping between an object or region in the merged 2D image to the respective object or region in the displayed (i.e., source or “best”) image may not necessarily be 1-to-1, and will possibly be “1-to-many” in certain circumstances, for example, when multiple line structures on different tomosynthesis image slices combine together to form a line-crossing structures in the synthesized 2D image. By way of example,
As explained above, this above described examples with respect to
In accordance with a further aspect of the disclosed inventions, the available features of the user interface may be extended to function, not only based point/location of the merged image, but also based in a similar fashion on a structure/object/region. For example, particular objects or region(s) in the merged image may be automatically highlighted when displayed, based on the system recognition of possible interest in the respective objects, or of objects located in the respective region(s). In one embodiment, shown in
In preferred embodiments, the system employs known image processing techniques to identify different breast tissue structures in the various source images, and highlight them in the merged image, in particular, tissue structures comprising or related to abnormal objects, such as micro-calcification clusters, round-or-lobulated masses, spiculated masses, architectural distortions, etc.; as well as benign tissue structures comprising or related to normal breast tissues, such as linear tissues, cysts, lymph nodes, blood vessels, etc. Furthermore, an object or region consisting of or containing a first type of tissue structure may be highlighted in a first manner in the displayed merged image, and an object or region consisting or containing a second type of tissue structure may be highlighted in a second manner different from the first manner in the displayed merged image.
In various embodiments, the user may input a command through the user interface selecting or otherwise identifying a certain type of tissue structure, and, in response to the received command, the system performs one or both of (i) automatically highlighting in the displayed merged image objects comprising the selected type of tissue structure and/or regions containing one or more objects comprising the selected type of tissue structure, and (ii) automatically concurrently displaying the respective source slice (or otherwise the slice with best depiction of) a tissue structure of the selected type in the breast image data, e.g., a most prominent one of the selected tissue structure type based on a comparison, if more than one is detected in the source image stack. Thus, when the user “click” on (or very close to) a micro-calcification spot/cluster in the merged 2D image, and the system automatically concurrently displays the source (or otherwise best) tomosynthesis image slice including the corresponding micro-calcification in 3D. By way of another example, a user can select (through the user interface) a region in the 2D merged image that has the appearance with radiating line patterns (often an indication of spiculated masses), and the system will concurrently display the source (or otherwise best) 3D tomosynthesis slice, or perhaps to a series of consecutive tomosynthesis slices, for viewing the radiating line patterns.
In various embodiments, the user may input a command through the user interface, activating dynamic display functionality, wherein the system automatically highlights those objects and tissue structures that (dynamically) correspond to the location of a user movable input device in the displayed merged image. In such embodiments, the system may further comprise automatically concurrently displaying a respective source image of a highlighted selected tissue structure that corresponds to a given location of a user movable input device in the displayed merged image, again, on a dynamic basis.
In one embodiment, the system can be activated to provide a “shadow” cursor is displayed on the right-hand-side monitor 126, in a location corresponding to the same (x,y) location as the user's actual curser on the left-hand-side monitor 124, so that moving the curser around in the 2D image moves the shadow curser in the tomosynthesis image at same X,Y coordinates. The reverse can also be implemented, i.e., with the active user curser operable in the right-hand monitor 126, and the show curser in the left-hand monitor 124. In one implementation, this dynamic display feature allows the system to follow the user's point of interest, e.g. mouse cursor location, in the 2d merged image, and dynamically display/highlight the most “meaningful” region(s) underneath in real time. For example, the user can move the mouse (without clicking any button) over a blood vessel, and the system will instantly highlight the vessel contour.
It should be appreciated that the presently disclosed inventions may be extended such that, rather than generate merely a synthesized 2D image and associated index/guidance map, the mapping concepts described herein may be extended to generate a fully mapped 3D volume, with each of the voxels in the mapped volume storing information related to the associated tomosynthesis slices(s) sourcing the particular voxel. For example, in one embodiment, the volume may be projected onto a fixed coordinate system, regardless of the actual volume of the breast. Projecting the volume to a fixed coordinate system in this manner facilitates processing of the image data, in particular, simplifying the correlation of voxels obtained during different acquisitions. For example, facilitating correlation of voxels in a 3D volume obtained from a CC acquisition of a breast with voxels in a volume obtained from an MLO acquisition of the same breast. In such an arrangement, one or more 3D maps may be provided, for example, to map from voxels in one slice of a 3D volume acquired via CC to one or more corresponding voxels in another volume, for example acquired via an MLO view. Such an arrangement facilitates comparison of slices obtained from different acquisitions that relate to a similar feature of interest within the breast volume, essentially permitting the medical professional to obtain a multi-planar review of a region of interest.
Having described exemplary embodiments, it can be appreciated that the examples described above and depicted in the accompanying figures are only illustrative, and that other embodiments and examples also are encompassed within the scope of the appended claims. For example, while the flow diagrams provided in the accompanying figures are illustrative of exemplary steps; the overall image merge process may be achieved in a variety of manners using other data merge methods known in the art. The system block diagrams are similarly representative only, illustrating functional delineations that are not to be viewed as limiting requirements of the disclosed inventions. Thus the above specific embodiments are illustrative, and many variations can be introduced on these embodiments without departing from the scope of the appended claims.
This application is a continuation of U.S. patent application Ser. No. 16/555,925, filed on Aug. 29, 2019, now issued as U.S. Pat. No. 10,977,863, which is a continuation of U.S. patent application Ser. No. 15/794,635, filed on Oct. 26, 2017, now issued as U.S. Pat. No. 10,410,417, which is a continuation of U.S. patent application Ser. No. 14/376,530, now issued as U.S. Pat. No. 9,805,507, which is a National Phase Entry under 35 U.S.C. § 371 of International Patent Application No. PCT/US2013/025993, having an international filing date of Feb. 13, 2013, which claims the benefit of priority under 35 U.S.C. § 119 to U.S. Provisional Patent Application No. 61/597,958, filed Feb. 13, 2012, and which is hereby incorporated by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
3502878 | Stewart et al. | Mar 1970 | A |
3863073 | Wagner | Jan 1975 | A |
3971950 | Evans et al. | Jul 1976 | A |
4160906 | Daniels | Jul 1979 | A |
4310766 | Finkenzeller et al. | Jan 1982 | A |
4496557 | Malen et al. | Jan 1985 | A |
4559641 | Caugant et al. | Dec 1985 | A |
4706269 | Reina et al. | Nov 1987 | A |
4744099 | Huettenrauch | May 1988 | A |
4773086 | Fujita | Sep 1988 | A |
4773087 | Plewes | Sep 1988 | A |
4819258 | Kleinman et al. | Apr 1989 | A |
4821727 | Levene et al. | Apr 1989 | A |
4907156 | Doi et al. | Mar 1990 | A |
4969174 | Schied | Nov 1990 | A |
4989227 | Tirelli et al. | Jan 1991 | A |
5018176 | Romeas et al. | May 1991 | A |
RE33634 | Yanaki | Jul 1991 | E |
5029193 | Saffer | Jul 1991 | A |
5051904 | Griffith | Sep 1991 | A |
5078142 | Siczek et al. | Jan 1992 | A |
5099846 | Hardy | Mar 1992 | A |
5129911 | Siczek et al. | Jul 1992 | A |
5133020 | Giger et al. | Jul 1992 | A |
5163075 | Lubinsky | Nov 1992 | A |
5164976 | Scheid et al. | Nov 1992 | A |
5199056 | Darrah | Mar 1993 | A |
5219351 | Teubner | Jun 1993 | A |
5240011 | Assa | Aug 1993 | A |
5279309 | Taylor et al. | Jan 1994 | A |
5280427 | Magnusson | Jan 1994 | A |
5289520 | Pellegrino et al. | Feb 1994 | A |
5343390 | Doi et al. | Aug 1994 | A |
5359637 | Webbe | Oct 1994 | A |
5365562 | Toker | Nov 1994 | A |
5386447 | Siczek | Jan 1995 | A |
5415169 | Siczek et al. | May 1995 | A |
5426685 | Pellegrino et al. | Jun 1995 | A |
5452367 | Bick | Sep 1995 | A |
5491627 | Zhang et al. | Feb 1996 | A |
5499097 | Ortyn et al. | Mar 1996 | A |
5506877 | Niklason et al. | Apr 1996 | A |
5526394 | Siczek | Jun 1996 | A |
5539797 | Heidsieck et al. | Jul 1996 | A |
5553111 | Moore | Sep 1996 | A |
5592562 | Rooks | Jan 1997 | A |
5594769 | Pellegrino | Jan 1997 | A |
5596200 | Sharma | Jan 1997 | A |
5598454 | Franetzki | Jan 1997 | A |
5609152 | Pellegrino et al. | Mar 1997 | A |
5627869 | Andrew et al. | May 1997 | A |
5642433 | Lee et al. | Jun 1997 | A |
5642441 | Riley et al. | Jun 1997 | A |
5647025 | Frost et al. | Jul 1997 | A |
5657362 | Giger et al. | Aug 1997 | A |
5668889 | Hara | Sep 1997 | A |
5671288 | Wilhelm et al. | Sep 1997 | A |
5712890 | Spivey et al. | Jan 1998 | A |
5719952 | Rooks | Feb 1998 | A |
5735264 | Siczek et al. | Apr 1998 | A |
5763871 | Ortyn et al. | Jun 1998 | A |
5769086 | Ritchart et al. | Jun 1998 | A |
5773832 | Sayed et al. | Jun 1998 | A |
5803912 | Siczek et al. | Sep 1998 | A |
5818898 | Tsukamoto et al. | Oct 1998 | A |
5828722 | Ploetz | Oct 1998 | A |
5835079 | Shieh | Nov 1998 | A |
5841124 | Ortyn et al. | Nov 1998 | A |
5872828 | Niklason | Feb 1999 | A |
5875258 | Ortyn et al. | Feb 1999 | A |
5878104 | Ploetz | Mar 1999 | A |
5878746 | Lemelson et al. | Mar 1999 | A |
5896437 | Ploetz | Apr 1999 | A |
5941832 | Tumey | Aug 1999 | A |
5954650 | Saito | Sep 1999 | A |
5986662 | Argiro | Nov 1999 | A |
6005907 | Ploetz | Dec 1999 | A |
6022325 | Siczek et al. | Feb 2000 | A |
6067079 | Shieh | May 2000 | A |
6075879 | Roehrig et al. | Jun 2000 | A |
6091841 | Rogers | Jul 2000 | A |
6101236 | Wang et al. | Aug 2000 | A |
6102866 | Nields et al. | Aug 2000 | A |
6137527 | Abdel-Malek | Oct 2000 | A |
6141398 | He | Oct 2000 | A |
6149301 | Kautzer et al. | Nov 2000 | A |
6175117 | Komardin | Jan 2001 | B1 |
6196715 | Nambu | Mar 2001 | B1 |
6215892 | Douglass et al. | Apr 2001 | B1 |
6216540 | Nelson | Apr 2001 | B1 |
6219059 | Argiro | Apr 2001 | B1 |
6256370 | Yavus | Apr 2001 | B1 |
6233473 | Sheperd | May 2001 | B1 |
6243441 | Zur | Jun 2001 | B1 |
6245028 | Furst et al. | Jun 2001 | B1 |
6272207 | Tang | Aug 2001 | B1 |
6289235 | Webber et al. | Sep 2001 | B1 |
6292530 | Yavus | Sep 2001 | B1 |
6293282 | Lemelson | Sep 2001 | B1 |
6327336 | Gingold et al. | Dec 2001 | B1 |
6327377 | Rutenberg et al. | Dec 2001 | B1 |
6341156 | Baetz | Jan 2002 | B1 |
6375352 | Hewes | Apr 2002 | B1 |
6389104 | Bani-Hashemi et al. | May 2002 | B1 |
6411836 | Patel | Jun 2002 | B1 |
6415015 | Nicolas | Jul 2002 | B2 |
6424332 | Powell | Jul 2002 | B1 |
6442288 | Haerer | Aug 2002 | B1 |
6459925 | Nields et al. | Oct 2002 | B1 |
6463181 | Duarte | Oct 2002 | B2 |
6468226 | McIntyre, IV | Oct 2002 | B1 |
6480565 | Ning | Nov 2002 | B1 |
6501819 | Unger et al. | Dec 2002 | B2 |
6556655 | Chichereau | Apr 2003 | B1 |
6574304 | Hsieh | Jun 2003 | B1 |
6597762 | Ferrant | Jul 2003 | B1 |
6611575 | Alyassin et al. | Aug 2003 | B1 |
6620111 | Stephens et al. | Sep 2003 | B2 |
6626849 | Huitema et al. | Sep 2003 | B2 |
6633674 | Barnes | Oct 2003 | B1 |
6638235 | Miller et al. | Oct 2003 | B2 |
6647092 | Eberhard | Nov 2003 | B2 |
6650928 | Gailly | Nov 2003 | B1 |
6683934 | Zhao | Jan 2004 | B1 |
6744848 | Stanton | Jun 2004 | B2 |
6748044 | Sabol et al. | Jun 2004 | B2 |
6751285 | Eberhard | Jun 2004 | B2 |
6758824 | Miller et al. | Jul 2004 | B1 |
6813334 | Koppe | Nov 2004 | B2 |
6882700 | Wang | Apr 2005 | B2 |
6885724 | Li | Apr 2005 | B2 |
6901156 | Giger et al. | May 2005 | B2 |
6912319 | Barnes | May 2005 | B1 |
6940943 | Claus | Sep 2005 | B2 |
6978040 | Berestov | Dec 2005 | B2 |
6987331 | Koeppe | Jan 2006 | B2 |
6999554 | Mertelmeier | Feb 2006 | B2 |
7022075 | Grunwald et al. | Apr 2006 | B2 |
7025725 | Dione et al. | Apr 2006 | B2 |
7030861 | Westerman | Apr 2006 | B1 |
7110490 | Eberhard | Sep 2006 | B2 |
7110502 | Tsuji | Sep 2006 | B2 |
7117098 | Dunlay et al. | Oct 2006 | B1 |
7123684 | Jing et al. | Oct 2006 | B2 |
7127091 | OpDeBeek | Oct 2006 | B2 |
7142633 | Eberhard | Nov 2006 | B2 |
7218766 | Eberhard | May 2007 | B2 |
7245694 | Jing et al. | Jul 2007 | B2 |
7289825 | Fors et al. | Oct 2007 | B2 |
7298881 | Giger et al. | Nov 2007 | B2 |
7315607 | Ramsauer | Jan 2008 | B2 |
7319735 | Defreitas et al. | Jan 2008 | B2 |
7323692 | Rowlands | Jan 2008 | B2 |
7346381 | Okerlund et al. | Mar 2008 | B2 |
7406150 | Minyard et al. | Jul 2008 | B2 |
7430272 | Jing et al. | Sep 2008 | B2 |
7443949 | Defreitas et al. | Oct 2008 | B2 |
7466795 | Eberhard et al. | Dec 2008 | B2 |
7577282 | Gkanatsios et al. | Aug 2009 | B2 |
7606801 | Faitelson et al. | Oct 2009 | B2 |
7616801 | Gkanatsios et al. | Nov 2009 | B2 |
7630533 | Ruth et al. | Dec 2009 | B2 |
7634050 | Muller et al. | Dec 2009 | B2 |
7640051 | Krishnan | Dec 2009 | B2 |
7697660 | Ning | Apr 2010 | B2 |
7702142 | Ren et al. | Apr 2010 | B2 |
7705830 | Westerman et al. | Apr 2010 | B2 |
7760924 | Ruth et al. | Jul 2010 | B2 |
7769219 | Zahniser | Aug 2010 | B2 |
7787936 | Kressy | Aug 2010 | B2 |
7809175 | Roehrig et al. | Oct 2010 | B2 |
7828733 | Zhang et al. | Nov 2010 | B2 |
7831296 | DeFreitas et al. | Nov 2010 | B2 |
7869563 | DeFreitas | Jan 2011 | B2 |
7974924 | Holla et al. | Jul 2011 | B2 |
7991106 | Ren et al. | Aug 2011 | B2 |
8044972 | Hall et al. | Oct 2011 | B2 |
8051386 | Rosander et al. | Nov 2011 | B2 |
8126226 | Bernard | Feb 2012 | B2 |
8155421 | Ren et al. | Apr 2012 | B2 |
8165365 | Bernard et al. | Apr 2012 | B2 |
8532745 | DeFreitas et al. | Sep 2013 | B2 |
8571289 | Ruth | Oct 2013 | B2 |
8594274 | Hoernig et al. | Nov 2013 | B2 |
8677282 | Cragun et al. | Mar 2014 | B2 |
8712127 | Ren et al. | Apr 2014 | B2 |
8897535 | Ruth et al. | Nov 2014 | B2 |
8983156 | Periaswamy et al. | Mar 2015 | B2 |
9020579 | Smith | Apr 2015 | B2 |
9075903 | Marshall | Jul 2015 | B2 |
9084579 | Ren et al. | Jul 2015 | B2 |
9119599 | Itai | Sep 2015 | B2 |
9129362 | Jerebko | Sep 2015 | B2 |
9289183 | Karssemeijer | Mar 2016 | B2 |
9451924 | Bernard | Sep 2016 | B2 |
9456797 | Ruth et al. | Oct 2016 | B2 |
9478028 | Parthasarathy | Oct 2016 | B2 |
9589374 | Gao | Mar 2017 | B1 |
9592019 | Sugiyama | Mar 2017 | B2 |
9805507 | Chen | Oct 2017 | B2 |
9808215 | Ruth et al. | Nov 2017 | B2 |
9811758 | Ren et al. | Nov 2017 | B2 |
9901309 | DeFreitas et al. | Feb 2018 | B2 |
10008184 | Kreeger et al. | Jun 2018 | B2 |
10010302 | Ruth et al. | Jul 2018 | B2 |
10092358 | DeFreitas | Oct 2018 | B2 |
10111631 | Gkanatsios | Oct 2018 | B2 |
10242490 | Karssemeijer | Mar 2019 | B2 |
10335094 | DeFreitas | Jul 2019 | B2 |
10357211 | Smith | Jul 2019 | B2 |
10410417 | Chen et al. | Sep 2019 | B2 |
10413263 | Ruth et al. | Sep 2019 | B2 |
10444960 | Marshall | Oct 2019 | B2 |
10456213 | DeFreitas | Oct 2019 | B2 |
10573276 | Kreeger et al. | Feb 2020 | B2 |
10575807 | Gkanatsios | Mar 2020 | B2 |
10595954 | DeFreitas | Mar 2020 | B2 |
10624598 | Chen | Apr 2020 | B2 |
10977863 | Chen | Apr 2021 | B2 |
10978026 | Kreeger | Apr 2021 | B2 |
20010038681 | Stanton et al. | Nov 2001 | A1 |
20010038861 | Hsu et al. | Nov 2001 | A1 |
20020012450 | Tsuji | Jan 2002 | A1 |
20020050986 | Inoue | May 2002 | A1 |
20020075997 | Unger et al. | Jun 2002 | A1 |
20020113681 | Byram | Aug 2002 | A1 |
20020122533 | Marie et al. | Sep 2002 | A1 |
20020188466 | Barrette et al. | Dec 2002 | A1 |
20020193676 | Bodicker | Dec 2002 | A1 |
20030007598 | Wang | Jan 2003 | A1 |
20030018272 | Treado et al. | Jan 2003 | A1 |
20030026386 | Tang | Feb 2003 | A1 |
20030048260 | Matusis | Mar 2003 | A1 |
20030073895 | Nields et al. | Apr 2003 | A1 |
20030095624 | Eberhard et al. | May 2003 | A1 |
20030097055 | Yanof | May 2003 | A1 |
20030128893 | Castorina | Jul 2003 | A1 |
20030135115 | Burdette et al. | Jul 2003 | A1 |
20030169847 | Karellas | Sep 2003 | A1 |
20030194050 | Eberhard | Oct 2003 | A1 |
20030194121 | Eberhard et al. | Oct 2003 | A1 |
20030195433 | Turovskiy | Oct 2003 | A1 |
20030210254 | Doan | Nov 2003 | A1 |
20030212327 | Wang | Nov 2003 | A1 |
20030215120 | Uppaluri | Nov 2003 | A1 |
20040008809 | Webber | Jan 2004 | A1 |
20040008900 | Jabri et al. | Jan 2004 | A1 |
20040008901 | Avinash | Jan 2004 | A1 |
20040036680 | Davis | Feb 2004 | A1 |
20040047518 | Tiana | Mar 2004 | A1 |
20040052328 | Saboi | Mar 2004 | A1 |
20040064037 | Smith | Apr 2004 | A1 |
20040066884 | Hermann Claus et al. | Apr 2004 | A1 |
20040066904 | Eberhard et al. | Apr 2004 | A1 |
20040070582 | Smith et al. | Apr 2004 | A1 |
20040077938 | Mark et al. | Apr 2004 | A1 |
20040081273 | Ning | Apr 2004 | A1 |
20040094167 | Brady | May 2004 | A1 |
20040101095 | Jing et al. | May 2004 | A1 |
20040109028 | Stern et al. | Jun 2004 | A1 |
20040109529 | Eberhard et al. | Jun 2004 | A1 |
20040127789 | Ogawa | Jul 2004 | A1 |
20040138569 | Grunwald | Jul 2004 | A1 |
20040171933 | Stoller et al. | Sep 2004 | A1 |
20040171986 | Tremaglio, Jr. et al. | Sep 2004 | A1 |
20040267157 | Miller et al. | Dec 2004 | A1 |
20050047636 | Gines et al. | Mar 2005 | A1 |
20050049521 | Miller et al. | Mar 2005 | A1 |
20050063509 | Defreitas et al. | Mar 2005 | A1 |
20050078797 | Danielsson et al. | Apr 2005 | A1 |
20050084060 | Seppi et al. | Apr 2005 | A1 |
20050089205 | Kapur | Apr 2005 | A1 |
20050105679 | Wu et al. | May 2005 | A1 |
20050107689 | Sasano | May 2005 | A1 |
20050111718 | MacMahon | May 2005 | A1 |
20050113681 | DeFreitas | May 2005 | A1 |
20050113715 | Schwindt et al. | May 2005 | A1 |
20050124845 | Thomadsen et al. | Jun 2005 | A1 |
20050135555 | Claus | Jun 2005 | A1 |
20050135664 | Kaufhold | Jun 2005 | A1 |
20050226375 | Eberhard | Oct 2005 | A1 |
20060009693 | Hanover et al. | Jan 2006 | A1 |
20060018526 | Avinash | Jan 2006 | A1 |
20060025680 | Jeune-Iomme | Feb 2006 | A1 |
20060030784 | Miller et al. | Feb 2006 | A1 |
20060074288 | Kelly et al. | Apr 2006 | A1 |
20060098855 | Gkanatsios | May 2006 | A1 |
20060129062 | Nicoson et al. | Jun 2006 | A1 |
20060132508 | Sadikali | Jun 2006 | A1 |
20060147099 | Marshall et al. | Jul 2006 | A1 |
20060155209 | Miller et al. | Jul 2006 | A1 |
20060197753 | Hotelling | Sep 2006 | A1 |
20060210131 | Wheeler | Sep 2006 | A1 |
20060228012 | Masuzawa | Oct 2006 | A1 |
20060238546 | Handley | Oct 2006 | A1 |
20060257009 | Wang | Nov 2006 | A1 |
20060269040 | Mertelmeier | Nov 2006 | A1 |
20060291618 | Eberhard et al. | Dec 2006 | A1 |
20070019846 | Bullitt et al. | Jan 2007 | A1 |
20070030949 | Jing et al. | Feb 2007 | A1 |
20070036265 | Jing et al. | Feb 2007 | A1 |
20070046649 | Reiner | Mar 2007 | A1 |
20070052700 | Wheeler et al. | Mar 2007 | A1 |
20070076844 | Defreitas et al. | Apr 2007 | A1 |
20070114424 | Danielsson et al. | May 2007 | A1 |
20070118400 | Morita et al. | May 2007 | A1 |
20070156451 | Gering | Jul 2007 | A1 |
20070223651 | Wagenaar et al. | Sep 2007 | A1 |
20070225600 | Weibrecht et al. | Sep 2007 | A1 |
20070236490 | Casteele | Oct 2007 | A1 |
20070242800 | Jing et al. | Oct 2007 | A1 |
20070263765 | Wu | Nov 2007 | A1 |
20070274585 | Zhang et al. | Nov 2007 | A1 |
20080019581 | Gkanatsios et al. | Jan 2008 | A1 |
20080043905 | Hassanpourgol | Feb 2008 | A1 |
20080045833 | Defreitas et al. | Feb 2008 | A1 |
20080101537 | Sendai | May 2008 | A1 |
20080114614 | Mahesh et al. | May 2008 | A1 |
20080125643 | Huisman | May 2008 | A1 |
20080130979 | Ren | Jun 2008 | A1 |
20080139896 | Baumgart | Jun 2008 | A1 |
20080152086 | Hall | Jun 2008 | A1 |
20080165136 | Christie et al. | Jul 2008 | A1 |
20080187095 | Boone et al. | Aug 2008 | A1 |
20080198966 | Hjarn | Aug 2008 | A1 |
20080221479 | Ritchie | Sep 2008 | A1 |
20080229256 | Shibaike | Sep 2008 | A1 |
20080240533 | Piron et al. | Oct 2008 | A1 |
20080297482 | Weiss | Dec 2008 | A1 |
20090003519 | Defreitas et al. | Jan 2009 | A1 |
20090005668 | West et al. | Jan 2009 | A1 |
20090010384 | Jing et al. | Jan 2009 | A1 |
20090034684 | Bernard et al. | Feb 2009 | A1 |
20090037821 | O'Neal et al. | Feb 2009 | A1 |
20090079705 | Sizelove et al. | Mar 2009 | A1 |
20090080594 | Brooks et al. | Mar 2009 | A1 |
20090080602 | Brooks et al. | Mar 2009 | A1 |
20090080604 | Shores et al. | Mar 2009 | A1 |
20090080752 | Ruth | Mar 2009 | A1 |
20090080765 | Bernard et al. | Mar 2009 | A1 |
20090087067 | Khorasani | Apr 2009 | A1 |
20090123052 | Ruth | May 2009 | A1 |
20090129644 | Daw et al. | May 2009 | A1 |
20090135997 | Defreitas et al. | May 2009 | A1 |
20090138280 | Morita et al. | May 2009 | A1 |
20090143674 | Nields | Jun 2009 | A1 |
20090167702 | Nurmi | Jul 2009 | A1 |
20090171244 | Ning | Jul 2009 | A1 |
20090238424 | Arakita | Sep 2009 | A1 |
20090259958 | Ban | Oct 2009 | A1 |
20090268865 | Ren et al. | Oct 2009 | A1 |
20090278812 | Yasutake | Nov 2009 | A1 |
20090296882 | Gkanatsios et al. | Dec 2009 | A1 |
20090304147 | Jing et al. | Dec 2009 | A1 |
20100034348 | Yu | Feb 2010 | A1 |
20100049046 | Peiffer | Feb 2010 | A1 |
20100054400 | Ren et al. | Mar 2010 | A1 |
20100079405 | Bernstein | Apr 2010 | A1 |
20100086188 | Ruth et al. | Apr 2010 | A1 |
20100088346 | Urness et al. | Apr 2010 | A1 |
20100098214 | Star-Lack et al. | Apr 2010 | A1 |
20100105879 | Katayose et al. | Apr 2010 | A1 |
20100121178 | Krishnan | May 2010 | A1 |
20100131294 | Venon | May 2010 | A1 |
20100131482 | Linthicum et al. | May 2010 | A1 |
20100135558 | Ruth et al. | Jun 2010 | A1 |
20100152570 | Navab | Jun 2010 | A1 |
20100166267 | Zhang | Jul 2010 | A1 |
20100195882 | Ren et al. | Aug 2010 | A1 |
20100208037 | Sendai | Aug 2010 | A1 |
20100231522 | Li | Sep 2010 | A1 |
20100246909 | Blum | Sep 2010 | A1 |
20100259561 | Forutanpour et al. | Oct 2010 | A1 |
20100259645 | Kaplan | Oct 2010 | A1 |
20100260316 | Stein et al. | Oct 2010 | A1 |
20100280375 | Zhang | Nov 2010 | A1 |
20100293500 | Cragun | Nov 2010 | A1 |
20110018817 | Kryze | Jan 2011 | A1 |
20110019891 | Puong | Jan 2011 | A1 |
20110054944 | Sandberg et al. | Mar 2011 | A1 |
20110069808 | Defreitas et al. | Mar 2011 | A1 |
20110069906 | Park | Mar 2011 | A1 |
20110087132 | DeFreitas et al. | Apr 2011 | A1 |
20110105879 | Masumoto | May 2011 | A1 |
20110109650 | Kreeger et al. | May 2011 | A1 |
20110110576 | Kreeger et al. | May 2011 | A1 |
20110150447 | Li | Jun 2011 | A1 |
20110163939 | Tam et al. | Jul 2011 | A1 |
20110178389 | Kumar et al. | Jul 2011 | A1 |
20110182402 | Partain | Jul 2011 | A1 |
20110234630 | Batman et al. | Sep 2011 | A1 |
20110237927 | Brooks et al. | Sep 2011 | A1 |
20110242092 | Kashiwagi | Oct 2011 | A1 |
20110310126 | Georgiev et al. | Dec 2011 | A1 |
20120014504 | Jang | Jan 2012 | A1 |
20120014578 | Karssemeijer | Jan 2012 | A1 |
20120069951 | Toba | Mar 2012 | A1 |
20120131488 | Karlsson et al. | May 2012 | A1 |
20120133600 | Marshall | May 2012 | A1 |
20120133601 | Marshall | May 2012 | A1 |
20120134464 | Hoernig et al. | May 2012 | A1 |
20120148151 | Hamada | Jun 2012 | A1 |
20120189092 | Jerebko | Jul 2012 | A1 |
20120194425 | Buelow | Aug 2012 | A1 |
20120238870 | Smith et al. | Sep 2012 | A1 |
20120293511 | Mertelmeier | Nov 2012 | A1 |
20130022165 | Jang | Jan 2013 | A1 |
20130044861 | Muller | Feb 2013 | A1 |
20130059758 | Haick | Mar 2013 | A1 |
20130108138 | Nakayama | May 2013 | A1 |
20130121569 | Yadav | May 2013 | A1 |
20130121618 | Yadav | May 2013 | A1 |
20130202168 | Jerebko | Aug 2013 | A1 |
20130259193 | Packard | Oct 2013 | A1 |
20140033126 | Kreeger | Jan 2014 | A1 |
20140035811 | Guehring | Feb 2014 | A1 |
20140064444 | Oh | Mar 2014 | A1 |
20140073913 | DeFreitas et al. | Mar 2014 | A1 |
20140219534 | Wiemker et al. | Aug 2014 | A1 |
20140219548 | Wels | Aug 2014 | A1 |
20140327702 | Kreeger et al. | Nov 2014 | A1 |
20140328517 | Gluncic | Nov 2014 | A1 |
20150052471 | Chen | Feb 2015 | A1 |
20150061582 | Smith | Apr 2015 | A1 |
20150238148 | Georgescu | Aug 2015 | A1 |
20150302146 | Marshall | Oct 2015 | A1 |
20150309712 | Marshall | Oct 2015 | A1 |
20150317538 | Ren et al. | Nov 2015 | A1 |
20150331995 | Zhao | Nov 2015 | A1 |
20160000399 | Halmann et al. | Jan 2016 | A1 |
20160022364 | DeFreitas et al. | Jan 2016 | A1 |
20160051215 | Chen | Feb 2016 | A1 |
20160078645 | Abdurahman | Mar 2016 | A1 |
20160140749 | Erhard | May 2016 | A1 |
20160228034 | Gluncic | Aug 2016 | A1 |
20160235380 | Smith | Aug 2016 | A1 |
20160367210 | Gkanatsios | Dec 2016 | A1 |
20170071562 | Suzuki | Mar 2017 | A1 |
20170262737 | Rabinovich | Sep 2017 | A1 |
20180047211 | Chen et al. | Feb 2018 | A1 |
20180137385 | Ren | May 2018 | A1 |
20180144244 | Masoud | May 2018 | A1 |
20180256118 | DeFreitas | Sep 2018 | A1 |
20190015173 | DeFreitas | Jan 2019 | A1 |
20190043456 | Kreeger et al. | Feb 2019 | A1 |
20190290221 | Smith | Sep 2019 | A1 |
20200046303 | DeFreitas | Feb 2020 | A1 |
20200093562 | DeFreitas | Mar 2020 | A1 |
20200184262 | Chui | Jun 2020 | A1 |
20200205928 | DeFreitas | Jul 2020 | A1 |
20200253573 | Gkanatsios | Aug 2020 | A1 |
20200345320 | Chen | Nov 2020 | A1 |
20200390404 | DeFreitas | Dec 2020 | A1 |
20210000553 | St. Pierre | Jan 2021 | A1 |
20210100518 | Chui | Apr 2021 | A1 |
20210100626 | St. Pierre | Apr 2021 | A1 |
20210113167 | Chui | Apr 2021 | A1 |
20210118199 | Chui | Apr 2021 | A1 |
20220013089 | Kreeger | Jan 2022 | A1 |
20220192615 | Chui | Jun 2022 | A1 |
20220386969 | Smith | Dec 2022 | A1 |
Number | Date | Country |
---|---|---|
2014339982 | Apr 2015 | AU |
1846622 | Oct 2006 | CN |
202161328 | Mar 2012 | CN |
102429678 | May 2012 | CN |
107440730 | Dec 2017 | CN |
102010009295 | Aug 2011 | DE |
102011087127 | May 2013 | DE |
775467 | May 1997 | EP |
982001 | Mar 2000 | EP |
1428473 | Jun 2004 | EP |
2236085 | Jun 2010 | EP |
2215600 | Aug 2010 | EP |
2301432 | Mar 2011 | EP |
2491863 | Aug 2012 | EP |
1986548 | Jan 2013 | EP |
2656789 | Oct 2013 | EP |
2823464 | Jan 2015 | EP |
2823765 | Jan 2015 | EP |
3060132 | Apr 2019 | EP |
H09-198490 | Jul 1997 | JP |
H09-238934 | Sep 1997 | JP |
H10-33523 | Feb 1998 | JP |
2000-200340 | Jul 2000 | JP |
2002-109510 | Apr 2002 | JP |
2002-282248 | Oct 2002 | JP |
2003-189179 | Jul 2003 | JP |
2003-199737 | Jul 2003 | JP |
2003-531516 | Oct 2003 | JP |
2006-519634 | Aug 2006 | JP |
2006-312026 | Nov 2006 | JP |
2007-130487 | May 2007 | JP |
2007-330334 | Dec 2007 | JP |
2007-536968 | Dec 2007 | JP |
2008-068032 | Mar 2008 | JP |
2009-034503 | Feb 2009 | JP |
2009-522005 | Jun 2009 | JP |
2009-526618 | Jul 2009 | JP |
2009-207545 | Sep 2009 | JP |
2010-137004 | Jun 2010 | JP |
2011-110175 | Jun 2011 | JP |
2012-501750 | Jan 2012 | JP |
2012011255 | Jan 2012 | JP |
2012-061196 | Mar 2012 | JP |
2013-244211 | Dec 2013 | JP |
2014-507250 | Mar 2014 | JP |
2014-534042 | Dec 2014 | JP |
2015-506794 | Mar 2015 | JP |
2015-144632 | Aug 2015 | JP |
2016-198197 | Dec 2015 | JP |
10-2015-0010515 | Jan 2015 | KR |
10-2017-0062839 | Jun 2017 | KR |
WO 9005485 | May 1990 | WO |
9317620 | Sep 1993 | WO |
9406352 | Mar 1994 | WO |
199700649 | Jan 1997 | WO |
WO 9816903 | Apr 1998 | WO |
WO 0051484 | Sep 2000 | WO |
WO 03020114 | Mar 2003 | WO |
WO 2005051197 | Jun 2005 | WO |
2005110230 | Nov 2005 | WO |
WO 2005110230 | Nov 2005 | WO |
2005112767 | Dec 2005 | WO |
WO 2005112767 | Dec 2005 | WO |
WO 2006055830 | May 2006 | WO |
WO 2006058160 | Jun 2006 | WO |
2007095330 | Aug 2007 | WO |
08014670 | Feb 2008 | WO |
WO 2008047270 | Apr 2008 | WO |
2008054436 | May 2008 | WO |
2009026587 | Feb 2009 | WO |
2010028208 | Mar 2010 | WO |
WO 2010059920 | May 2010 | WO |
WO 2011008239 | Jan 2011 | WO |
2011043838 | Apr 2011 | WO |
WO 2011065950 | Jun 2011 | WO |
WO 2011073864 | Jun 2011 | WO |
WO 2011091300 | Jul 2011 | WO |
2012001572 | Jan 2012 | WO |
2012068373 | May 2012 | WO |
WO 2012063653 | May 2012 | WO |
2012112627 | Aug 2012 | WO |
2012122399 | Sep 2012 | WO |
2013001439 | Jan 2013 | WO |
2013035026 | Mar 2013 | WO |
2013078476 | May 2013 | WO |
2013123091 | Aug 2013 | WO |
2014149554 | Sep 2014 | WO |
2014207080 | Dec 2014 | WO |
2015061582 | Apr 2015 | WO |
2015066650 | May 2015 | WO |
2015130916 | Sep 2015 | WO |
2016103094 | Jun 2016 | WO |
2016184746 | Nov 2016 | WO |
2018183548 | Oct 2018 | WO |
2018183549 | Oct 2018 | WO |
2018183550 | Oct 2018 | WO |
2018236565 | Dec 2018 | WO |
Entry |
---|
Van Schie, Guido, et al., “Mass detection in reconstructed digital breast tomosynthesis volumes with a computer-aided detection system trained on 2D mammograms”, Med. Phys. 40(4), Apr. 2013, 41902-1-41902-11. |
Van Schie, Guido, et al., “Generating Synthetic Mammograms from Reconstructed Tomosynthesis Volumes”, IEEE Transactions on Medical Imaging, vol. 32, No. 12, Dec. 2013, 2322-2331. |
Mikko Lilja, “Fast and accurate voxel projection technique in free-form cone-beam geometry with application to algebraic reconstruction,” Applies Sciences on Biomedical and Communication Technologies, 2008, Isabel '08, first international symposium on, IEEE, Piscataway NJ, Oct. 25, 2008. |
Pediconi, “Color-coded automated signal intensity-curve for detection and characterization of breast lesions: Preliminary evaluation of new software for MR-based breast imaging,” International Congress Series 1281 (2005) 1081-1086. |
Heang-Ping, Roc “Study of the effect of stereoscopic imaging on assessment of breast lesions,” Medical Physics, vol. 32, No. 4, Apr. 2005. |
Amendment Response to Final Office Action for U.S. Appl. No. 12/276,006 dated Mar. 24, 2010 (6 pages). |
Amendment Response to Non-Final Office Action for U.S. Appl. No. 12/276,006 dated Sep. 28, 2009 (8 pages). |
Final Office Action dated Jan. 20, 2010 for U.S. Appl. No. 12/276,006. |
Non-Final Office Action dated Jun. 25, 2009 for U.S. Appl. No. 12/276,006. |
Amendment Resonse after Final Office Action for U.S. Appl. No. 12/471,981 dated Apr. 3, 2013 (6 pages). |
Amendment Response to Non-Final Office Action for U.S. Appl. No. 12/471,981 dated Dec. 10, 2012 (6 pages). |
Non-Final Office Action dated Feb. 13, 2013 for U.S. Appl. No. 12/471,981. |
Non-Final Office Action dated Aug. 10, 2012 for U.S. Appl. No. 12/471,981. |
Amendment Response to Non-Final Office Action for U.S. Appl. No. 14/044,959 dated May 13, 2014 (8 pages). |
Non-Final Office Action dated Feb. 13, 2014 for U.S. Appl. No. 14/044,959. |
Foreign Office Action for CN Application No. 200980101409.X dated Jun. 26, 2014. |
Foreign Office Action for EP Patent Application No. 09796173.4 dated Apr. 11, 2014. |
Foreign Office Action for JP Patent Application No. 2011-537644 dated Jul. 29, 2013. |
Foreign Office Action for JP Patent Application No. 2014-047021 dated Jan. 21, 2015. |
International Search Report for International Patent Application No. PCT/US2009/065288 dated Jan. 29, 2014. |
International Preliminary Report on Patentability for International Publication No. PCT/US2012/066526 dated May 27, 2014. |
PCT Notification of International Search Report and Written Opinion for PCT/US2012/066526, Applicant Hologic, Inc., dated Feb. 6, 2013 (7 pages). |
International Preliminary Report on Patentability for International Publication No. PCT/US2013/025993 dated Aug. 19, 2014. |
International Search Report and Written Opinion for International Publication No. PCT/US2013/025993 dated Apr. 26, 2013. |
Foreign office action from JP 2014-543604 dated Oct. 4, 2016. |
Extended EP Search Report for EP Application No. 13749870.5 dated Oct. 7, 2015, 7 pages. |
Extended EP Search Report for EP Application No. 12851085.6, dated Jan. 6, 2015, 6 pages. |
Giger et al. “Development of a smart workstation for use in mammography”, in Proceedings of SPIE, vol. 1445(1991), p. 101 103; 4 pages. |
Giger et al., “An Intelligent Workstation for Computer-aided Diagnosis”, in RadioGraphics, May 1993, 13:3 pp. 647 656; 10 pages. |
Non final office action dated Jan. 22, 2016 for U.S. Appl. No. 14/360,389. |
“Predicting tumour location by simulating large deformations of the breast using a 3D finite element model and nonlinear elasticity” by P. Pathmanathan et al., Medical Image Computing and Computer-Assisted Intervention, pp. 217-224, vol. 3217 (2004). |
“ImageParser: a tool for finite element generation from three-dimensional medical images” by H. M. Yin et al., BioMedical Engineering Online. 3:31, pp. 1-9, Oct. 1, 2004. |
“Biomechanical 3-D Finite Element Modeling of the Human Breast Using MRI Data” by A. Samani et al. IEEE Transactions on Medical Imaing, vol. 20, No. 4, pp. 271-279. 2001. |
“Mammogram synthesis using a 3D simulation. I. breast tissue model and image acquisition simulation” by Bakic et al., Medical Physics. 29, pp. 2131-2139 (2002). |
Non Final Office action dated Nov. 20, 2015 for U.S. Appl. No. 14/549,604. |
Response to Non Final Office action dated May 23, 2016 for U.S. Appl. No. 14/360,389. |
Final Office Action dated Jul. 5, 2016 for U.S. Appl. No. 14/360,389. |
Response to Final Office Action dated Aug. 15, 2016 for U.S. Appl. No. 14/360,389. |
Advisory Action dated Aug. 24, 2016 for U.S. Appl. No. 14/360,389. |
Pre-Appeal Brief Request for Review submitted Oct. 4, 2016 for U.S. Appl. No. 14/360,389. |
Appeal Brief submitted Dec. 4, 2016 for U.S. Appl. No. 14/360,389. |
Examiner's Answer to Appeal Brief dated Jan. 31, 2017 for U.S. Appl. No. 14/360,389. |
Reply Brief submitted Mar. 6, 2017 for U.S. Appl. No. 14/360,389. |
Decision on Appeal mailed Nov. 8, 2017 for U.S. Appl. No. 14/360,389. |
Non-Final Office Action dated Mar. 9, 2017 for U.S. Appl. No. 15/088,844. |
Notice of Allowance for U.S. Appl. No. 15/088,844 dated Jun. 29, 2017. |
Notice of Allowance for U.S. Appl. No. 15/088,844 dated Mar. 28, 2017. |
Office Action dated Mar. 10, 2017 for Canadian Application No. 2,702,782, Owner Hologic, Inc., based on PCT/US2009/065288, 3 pages. |
Office Action dated Jan. 11, 2017 for Japanese Patent Application No. 2014-556824, Applicant Hologic, Inc., including English Translation provided by Japanese associate, 12 pages. |
Computer generated translation of Foreign Patent Reference JP 2003-189179 A, published Jul. 4, 2003, 16 pages. |
International Preliminary Report on Patentability for International Publication No. PCT/US2009/065288 dated Feb. 18, 2014. |
Notice of Allowance dated Jan. 22, 2018 for U.S. Appl. No. 14/360,389. |
Office action dated Feb. 1, 2018 for U.S. Appl. No. 15/802,225. |
Office Action dated Feb. 19, 2018 for EP Application 12851085.6, Applicant Hologic, Inc. 5 pp. |
Extended EP Search Report for EP Application No. 17176956.5 dated Apr. 3, 2018, 7 pages. |
Office action dated Aug. 27, 2018 for U.S. Appl. No. 15/794,635. |
Amendment response to office action filed Nov. 14, 2018 for U.S. Appl. No. 15/794,635. |
Notice of Allowance dated Jan. 17, 2019 for U.S. Appl. No. 15/794,635. |
Non Final office Action dated Jan. 25, 19 for U.S. Appl. No. 16/013,782. |
European search report in connection with corresponding European patent application No. EP 06255790, dated Aug. 17, 2007. |
European search report in connection with counterpart European Patent Application No. 05824734, dated May 9, 2011. |
PCT International Search Report and Written Opinion dated Sep. 25, 2008, for International Application No. PCT/US2005/041941, Applicant Hologic, Inc., 8 pages. |
Amendment After Non-Final Office Action filed Apr. 12, 2019 for U.S. Appl. No. 16/013,782. |
Non Final Office Action dated Sep. 21, 2016 for U.S. Appl. No. 14/744,930. |
Response to Non Final Office action filed Dec. 14, 2016 for U.S. Appl. No. 14/744,930. |
Final Office Action dated Mar. 31, 2017 for U.S. Appl. No. 14/744,930. |
Response to Final Office action filed Aug. 2, 2017 for U.S. Appl. No. 14/744,930. |
Non Final Office action dated May 18, 2018 for U.S. Appl. No. 15/804,915. |
Response to Non Final Office Action filed Aug. 20, 2018 for U.S. Appl. No. 15/804,915. |
Non-Final Office Action dated Jun. 27, 2019 for U.S. Appl. No. 16/013,701. |
Al Sallab et al., “Self Learning Machines Using Deep Networks”, Soft Computing and Pattern Recognition (SoCPaR), 2011 Int'l. Conference of IEEE, Oct. 14, 2011, pp. 21-26. |
Ghiassi, M. et al., “A Dynamic Architecture for Artificial Networks”, Neurocomputing, vol. 63, Aug. 20, 2004, pp. 397-413. |
Caroline, B.E. et al., “Computer aided detection of masses in digital breast tomosynthesis: A review”, 2012 International Conference on Emerging Trends in Science, Engineering and Technology (INCOSET), Tiruchirappalli, 2012, pp. 186-191. |
Ertas, M. et al., “2D versus 3D total variation minimization in digital breast tomosynthesis”, 2015 IEEE International Conference on Imaging Systems and Techniques (IST), Macau, 2015, pp. 1-4. |
EFilm Mobile HD by Merge Healthcare, web site: http://itunes.apple.com/bw/app/efilm-mobile-hd/id405261243?mt=8, accessed on Nov. 3, 2011 (2 pages). |
EFilm Solutions, eFilm Workstation (tm) 3.4, website: http://estore.merge.com/na/estore/content.aspx?productID=405, accessed on Nov. 3, 2011 (2 pages). |
Wodajo, Felasfa, MD, “Now Playing: Radiology Images from Your Hospital PACS on your iPad,” Mar. 17, 2010; web site: http://www.imedicalapps.com/2010/03/now-playing-radiology-images-from-your-hospital-pacs-on-your-ipad/, accessed on Nov. 3, 2011 (3 pages). |
Lewin,JM, et al., Dual-energy contrast-enhanced digital subtraction mammography: feasibility. Radiology 2003; 229:261-268. |
Berg, WA et al., “Combined screening with ultrasound and mammography vs mammography alone in women at elevated risk of breast cancer”, JAMA 299:2151-2163, 2008. |
Carton, AK, et al., “Dual-energy contrast-enhanced digital breast tomosynthesis—a feasibility study”, Br J Radiol. Apr. 2010;83 (988):344-50. |
Chen, SC, et al., “Initial clinical experience with contrast-enhanced digital breast tomosynthesis”, Acad Radio. Feb. 2007 14(2):229-38. |
Diekmann, F., et al., “Digital mammography using iodine-based contrast media: initial clinical experience with dynamic contrast medium enhancement”, Invest Radiol 2005; 40:397-404. |
Dromain C., et al., “Contrast enhanced spectral mammography: a multi-reader study”, RSNA 2010, 96th Scientific Assembly and Scientific Meeting. |
Dromain, C., et al., “Contrast-enhanced digital mammography”, Eur J Radiol. 2009; 69:34-42. |
Freiherr, G., “Breast tomosynthesis trials show promise”, Diagnostic Imaging—San Francisco 2005, V27; N4:42-48. |
ICRP Publication 60: 1990 Recommendations of the International Commission on Radiological Protection, 12 pages. |
Jochelson, M., et al., “Bilateral Dual Energy contrast-enhanced digital mammography: Initial Experience”, RSNA 2010, 96th Scientific Assembly and Scientific Meeting, 1 page. |
Jong, RA, et al., Contrast-enhanced digital mammography: initial clinical experience. Radiology 2003; 228:842-850. |
Kopans, et al. Will tomosynthesis replace conventional mammography? Plenary Session SFN08: RSNA 2005. |
Lehman, CD, et al. MRI evaluation of the contralateral breast in women with recently diagnosed breast cancer. N Engl J Med 2007; 356:1295-1303. |
Lindfors, KK, et al., Dedicated breast CT: initial clinical experience. Radiology 2008; 246(3): 725-733. |
Niklason, L., et al., Digital tomosynthesis in breast imaging. Radiology. Nov. 1997; 205(2):399-406. |
Poplack, SP, et al., Digital breast tomosynthesis: initial experience in 98 women with abnormal digital screening mammography. AJR Am J Roentgenology Sep. 2007 189(3):616-23. |
Prionas, ND, et al., Contrast-enhanced dedicated breast CT: initial clinical experience. Radiology. Sep. 2010 256(3):714-723. |
Rafferty, E. et al., “Assessing Radiologist Performance Using Combined Full-Field Digital Mammography and Breast Tomosynthesis Versus Full-Field Digital Mammography Alone: Results”. . . presented at 2007 Radiological Society of North America meeting, Chicago IL. |
Smith, A., “Full field breast tomosynthesis”, Radiol Manage. Sep.-Oct. 2005; 27(5):25-31. |
Weidner N, et al., “Tumor angiogenesis and metastasis: correlation in invasive breast carcinoma”, New England Journal of Medicine 1991; 324:1-8. |
Weidner, N, “The importance of tumor angiogenesis: the evidence continues to grow”, Am J Clin Pathol. Nov. 2004 122(5):696-703. |
Hologic, Inc., 510(k) Summary, prepared Nov. 28, 2010, for Affirm Breast Biopsy Guidance System Special 510(k) Premarket Notification, 5 pages. |
Hologic, Inc., 510(k) Summary, prepared Aug. 14, 2012, for Affirm Breast Biopsy Guidance System Special 510(k) Premarket Notification, 5 pages. |
“Filtered Back Projection”, (NYGREN), published May 8, 2007, URL: http://web.archive.org/web/19991010131715/http://www.owlnet.rice.edu/˜elec539/Projects97/cult/node2.html, 2 pgs. |
Hologic, “Lorad StereoLoc II” Operator's Manual 9-500-0261, Rev. 005, 2004, 78 pgs. |
Shrading, Simone et al., “Digital Breast Tomosynthesis-guided Vacuum-assisted Breast Biopsy: Initial Experiences and Comparison with Prone Stereotactic Vacuum-assisted Biopsy”, the Department of Diagnostic and Interventional Radiology, Univ. of Aachen, Germany, published Nov. 12, 2014, 10 pgs. |
“Supersonic to feature Aixplorer Ultimate at ECR”, AuntiMinnie.com, 3 pages (Feb. 2018). |
Bushberg, Jerrold et al., “The Essential Physics of Medical Imaging”, 3rd ed., In: “The Essential Physics of Medical Imaging, Third Edition”, Dec. 28, 2011, Lippincott & Wilkins, Philadelphia, PA, USA, XP05579051, pp. 270-272. |
Dromain, Clarisse et al., “Dual-energy contrast-enhanced digital mammography: initial clinical results”, European Radiology, Sep. 14, 2010, vol. 21, pp. 565-574. |
Reynolds, April, “Stereotactic Breast Biopsy: A Review”, Radiologic Technology, vol. 80, No. 5, Jun. 1, 2009, pp. 447M-464M, XP055790574. |
E. Shaw de Paredes et al., “Interventional Breast Procedure”, published Sep./Oct. 1998 in Curr Probl Diagn Radiol, pp. 138-184. |
Burbank, Fred, “Stereotactic Breast Biopsy: Its History, Its Present, and Its Future”, published in 1996 at the Southeastern Surgical Congress, 24 pages. |
Georgian-Smith, Dianne, et al., “Stereotactic Biopsy of the Breast Using an Upright Unit, a Vacuum-Suction Needle, and a Lateral Arm-Support System”, 2001, at the American Roentgen Ray Society meeting, 8 pages. |
Fischer Imaging Corp, Mammotest Plus manual on minimally invasive breast biopsy system, 2002, 8 pages. |
Fischer Imaging Corporation, Installation Manual, MammoTest Family of Breast Biopsy Systems, 86683G, 86684G, P-55957-IM, Issue 1, Revision 3, Jul. 2005, 98 pages. |
Fischer Imaging Corporation, Operator Manual, MammoTest Family of Breast Biopsy Systems, 86683G, 86684G, P-55956-OM, Issue 1, Revision 6, Sep. 2005, 258 pages. |
Koechli, Ossi R., “Available Sterotactic Systems for Breast Biopsy”, Renzo Brun del Re (Ed.), Minimally Invasive Breast Biopsies, Recent Results in Cancer Research 173:105-113; Springer-Verlag, 2009. |
Conner, Peter, “Breast Response to Menopausal Hormone Therapy—Aspects on Proliferation, apoptosis and Mammographic Density”, 2007 Annals of Medicine, 39;1, 28-41. |
Glick, Stephen J., “Breast CT”, Annual Rev. Biomed. Eng., 2007, 9;501-26. |
Metheany, Kathrine G. et al., “Characterizing anatomical variability in breast CT images”, Oct. 2008, Med. Phys. 35 (10); 4685-4694. |
Dromain, Clarisse, et al., “Evaluation of tumor angiogenesis of breast carcinoma using contrast-enhanced digital mammography”, AJR: 187, Nov. 2006, 16 pages. |
Zhao, Bo, et al., “Imaging performance of an amorphous selenium digital mammography detector in a breast tomosynthesis system”, May 2008, Med. Phys 35(5); 1978-1987. |
Mahesh, Mahadevappa, “AAPM/RSNA Physics Tutorial for Residents—Digital Mammography: An Overview”, Nov.-Dec. 2004, vol. 24, No. 6, 1747-1760. |
Zhang, Yiheng et al., “A comparative study of limited-angle cone-beam reconstruction methods for breast tomosythesis”, Med Phys., Oct. 2006, 33(10): 3781-3795. |
Sechopoulos, et al., “Glandular radiation dose in tomosynthesis of the breast using tungsten targets”, Journal of Applied Clinical Medical Physics, vol. 8, No. 4, Fall 2008, 161-171. |
Wen, Junhai et al., “A study on truncated cone-beam sampling strategies for 3D mammography”, 2004, IEEE, 3200-3204. |
Ijaz, Umer Zeeshan, et al., “Mammography phantom studies using 3D electrical impedance tomography with numerical forward solver”, Frontiers in the Convergence of Bioscience and Information Technologies 2007, 379-383. |
Kao, Tzu-Jen et al., “Regional admittivity spectra with tomosynthesis images for breast cancer detection”, Proc. Of the 29th Annual Int'l. Conf. of the IEEE EMBS, Aug. 23-26, 2007, 4142-4145. |
Varjonen, Mari, “Three-Dimensional Digital Breast Tomosynthesis in the Early Diagnosis and Detection of Breast Dancer”, IWDM 2006, LNCS 4046, 152-159. |
Taghibakhsh, f. et al., “High dynamic range 2-TFT amplified pixel sensor architecture for digital mammography tomosynthesis”, IET Circuits Devices Syst., 2007, 1(10, pp. 87-92. |
Chan, Heang-Ping et al., “Computer-aided detection system for breast masses on digital tomosynthesis mammograms: Preliminary Experience”, Radiology, Dec. 2005, 1075-1080. |
European Decision to Refuse a European Patent Application in Application 18207785.9, dated May 19, 2022, 23 pages. |
European Search Opinion in Application 18207785.9, dated Feb. 12, 2019, 2 pages. |
European Summons to Attend Oral Proceedings in Application 18207785.9, mailed Aug. 17, 2021, 8 pages. |
European Minutes of the Oral Proceedings in Application 18207785.9, mailed Apr. 8, 2022, 5 pages. |
European Brief Communication in Application 18207785.9, mailed Feb. 21, 2022, 55 pages. |
European Submission as Filed further to Appeal in Application 09796173.4, filed Jun. 13, 2022, 24 pages. |
Diekmann, Felix et al., “Thick Slices from Tomosynthesis Data Sets: Phantom Study for the Evaluation of Different Algorithms”, Journal of Digital Imaging, Springer, vol. 22, No. 5, Oct. 23, 2007, pp. 519-526. |
Kopans, Daniel B., “Breast Imaging”, 3rd Edition, Lippincott Williams and Wilkins, published Nov. 2, 2006, pp. 960-967. |
Williams, Mark B. et al., “Optimization of exposure parameters in full field digital mammography”, Medical Physics 35, 2414 (May 20, 2008); doi: 10.1118/1.2912177, pp. 2414-2423. |
Elbakri, Idris A. et al., “Automatic exposure control for a slot scannong full field digital mammagraphy system”, Med. Phys. 2005; Sep; 32(9):2763-2770, Abstract only. |
Feng, Steve Si Jia, et al., “Clinical digital breast tomosynthesis system: Dosimetric Characterization”, Radiology, Apr. 2012, 263(1); pp. 35-42. |
Number | Date | Country | |
---|---|---|---|
20220005277 A1 | Jan 2022 | US |
Number | Date | Country | |
---|---|---|---|
61597958 | Feb 2012 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 16555925 | Aug 2019 | US |
Child | 17200754 | US | |
Parent | 15794635 | Oct 2017 | US |
Child | 16555925 | US | |
Parent | 14376530 | US | |
Child | 15794635 | US |