The presently disclosed inventions relate generally to breast imaging techniques such as tomosynthesis, and more specifically to systems and methods for obtaining, processing, synthesizing, storing and displaying a breast imaging data set or a subset thereof. In particular, the present disclosure relates to creating a high-dimensional grid by decomposing high-dimensional data to lower-dimensional data in order to identify objects to display in one or more synthesized images.
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 image data, and to also provide other benefits. Further, substantial attention and technological development have been dedicated to obtaining three-dimensional images of the breast using methods such as breast tomosynthesis. In contrast to the 2D 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 mathematically reconstructed on planes typically 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 user (e.g., a radiologist or other medical professional) to scroll through the image slices to view only the structures in that slice.
Imaging systems such as 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 introduced systems that include tomosynthesis imaging; e.g., which do not include the ability to also acquire a mammogram in the same compression.
Examples of systems and methods that leverage existing medical expertise in order to facilitate, optionally, 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 optionally be displayed along with tomosynthesis projection or reconstructed images, in order to assist in screening and diagnosis.
The 2D synthesized image is designed to provide a concise representation of the 3D reconstruction slices, including any clinically important and meaningful information, such as abnormal lesions and normal breast structures, while representing in relevant part a traditional 2D image. There are many different types of lesions and breast structures, which may be defined as different types of image objects having different characteristics. For any given image object visible in the 3D volume data, it is important to maintain and enhance the image characteristics (e.g., micro-calcifications, architectural distortions, etc.), as much as possible, onto the 2D synthesized image. To achieve the enhancement of the targeted image object, it is critical to accurately identify and represent the image object present in the 3D tomosynthesis data.
In one embodiment of the disclosed inventions, a method for processing breast tissue image data includes obtaining image data of a patient's breast tissue, and processing the image data to generate a set of image slices that collectively depict the patient's breast tissue. One or more filters associated with a plurality of multi-level feature modules are then applied to each image slice, the multi-level feature modules being configured to and recognize at least one assigned feature of a high-dimensional object that may be present in the patient's breast tissue, wherein the method further includes at each multi-level feature module, generating a feature map depicting regions (if any) of the respective image slice having the at least one assigned feature. The generated feature maps are then combined into an object map, preferably by using a learning library-based combiner, wherein the object map indicates a probability that the respective high-dimensional object is present at a particular location of the image slice. The method may further include creating a 2D synthesized image identifying one or more high-dimensional objects based at least in part on object maps generated for a plurality of image slices.
These and other aspects and embodiments of the disclosed inventions are described in more detail below, in conjunction with the accompanying figures.
The drawings illustrate the design and utility of embodiments of the disclosed inventions, in which similar elements are referred to by common reference numerals. These drawings are not necessarily drawn to scale. In order to better appreciate how the above-recited and other advantages and objects are obtained, a more particular description of the embodiments will be rendered, which are illustrated in the accompanying drawings. These drawings depict only typical embodiments of the disclosed inventions and are not therefore to be considered limiting of its scope.
All numeric values are herein assumed to be modified by the terms “about” or “approximately,” whether or not explicitly indicated, wherein the terms “about” and “approximately” generally refer to a range of numbers that one of skill in the art would consider equivalent to the recited value (i.e., having the same function or result). In some instances, the terms “about” and “approximately” may include numbers that are rounded to the nearest significant figure. The recitation of numerical ranges by endpoints includes all numbers within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5).
As used in this specification and the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the content clearly dictates otherwise. As used in this specification and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise. 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.
Various embodiments of the disclosed inventions are described hereinafter with reference to the figures. It should be noted that the figures are not drawn to scale and that elements of similar structures or functions are represented by like reference numerals throughout the figures. It should also be noted that the figures are only intended to facilitate the description of the embodiments. They are not intended as an exhaustive description of the invention or as a limitation on the scope of the disclosed inventions, which is defined only by the appended claims and their equivalents. In addition, an illustrated embodiment of the disclosed inventions needs not have all the aspects or advantages shown. For example, an aspect or an advantage described in conjunction with a particular embodiment of the disclosed inventions is not necessarily limited to that embodiment and can be practiced in any other embodiments even if not so illustrated.
For the following defined terms and abbreviations, these definitions shall be applied throughout this patent specification and the accompanying claims, unless a different definition is given in the claims or elsewhere in this specification:
An “acquired image” refers to an image generated while visualizing a patient's tissue. Acquired images can be generated by radiation from a radiation source impacting on a radiation detector disposed on opposite sides of a patient's tissue, as in a conventional mammogram.
A “reconstructed image” refers to an image generated from data derived from a plurality of acquired images. A reconstructed image simulates an acquired image not included in the plurality of acquired images.
A “synthesized image” refers to an artificial image generated from data derived from a plurality of acquired and/or reconstructed images. A synthesized image includes elements (e.g., objects and regions) from the acquired and/or reconstructed images, but does not necessarily correspond to an image that can be acquired during visualization. Synthesized images are constructed analysis tools.
An “Mp” image is 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 (e.g., to a health professional), storage (e.g., in the PACS system of a hospital), and/or other use.
A “Tp” image is 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, storage, and/or other use.
A “Tr” image is type (or subset) of a reconstructed image that is reconstructed from tomosynthesis projection images Tp, for example, in the manner described in one or more of U.S. Pat. Nos. 7,577,282, 7,606,801, 7,760,924, and 8,571,289, 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.
An “Ms” image is a type (or subset) of a synthesized image, in particular, a synthesized 2D projection image that simulates mammography images, such as a craniocaudal (CC) or mediolateral oblique (MLO) images, and is constructed using tomosynthesis projection images Tp, tomosynthesis reconstructed images Tr, or a combination thereof. Ms images may be provided for display to a health professional or for storage in the PACS system of a hospital or another institution. Examples of methods that may be used to generate Ms images are described in the above-incorporated U.S. Pat. Nos. 7,760,924 and 8,571,289.
It should be appreciated that Tp, Tr, Ms and Mp image data encompasses information, in whatever form, that is sufficient to describe the respective image for display, further processing, or storage. The respective 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) and mammography images (Ms and Mp) are matched to a common coordinate system, as described in U.S. Pat. No. 7,702,142. 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.
The terms “generating an image” and “transmitting an image” respectively refer to generating and transmitting information that is sufficient to describe the image for display. The generated and transmitted information is typically digital information.
In order to ensure that a synthesized 2D image displayed to an end-user (e.g., an Ms image) includes the most clinically relevant information, it is necessary to detect and identify three-dimensional (3D) objects, such as malignant breast mass, tumors, etc., within the breast tissue. This information may be used to create a high-dimensional grid, e.g., a 3D grid, that helps create a more accurate and enhanced rendering of the most important features in the synthesized 2D image. The present disclosure describes one approach for creating a 3D grid by decomposing high-dimensional objects (i.e., 3D or higher) into lower-dimensional image patterns (2D images). When these 2D image patterns are detected in a tomosynthesis stack of images, they may be combined using a learning library that determines a location and morphology of the corresponding 3D object within the patient's breast tissue. This information regarding the presence of the respective 3D object(s) enables the system to render a more accurate synthesized 2D image to an end-user.
More particularly, the image generation and display system 100 includes an image acquisition system 101 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 101, or from the storage device 102, or both, to a computer system configured as a reconstruction engine 103 that reconstructs the Tp images into reconstructed image “slices” Tr, representing breast slices of selected thickness and at selected orientations, as disclosed in the above-incorporated patents and applications.
Mode filters 107 are disposed between image acquisition and image display. The filters 107 may additionally include customized filters for each type of image (i.e., Tp, Mp, and Tr images) 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. For example, filters programmed for recognizing objects across various 2D image slices may be applied in order to detect image patterns that may belong to a particular high-dimensional objects. 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
The imaging and display system 100 further includes a hierarchical multi-level feature 2D synthesizer 104 that operates substantially in parallel with the reconstruction engine 103 for generating 2D synthesized images using a combination of one or more Tp, Mp, and/or Tr images. The hierarchical multi-level feature 2D synthesizer 104 consumes a set of input images (e.g., Mp, Tr and/or Tp images), determines a set of most relevant features from each of the input images, and outputs one or more synthesized 2D images. The synthesized 2D image represents a consolidated synthesized image that condenses significant portions of various slices onto one image. This provides an end-user (e.g., medical personnel, radiologist, etc.) with the most clinically-relevant image data in an efficient manner, and reduces time spent on other images that may not have significant data.
One type of relevant image data to highlight in the synthesized 2D images would be relevant objects found across one or more Mp, Tr and/or Tp images. Rather than simply assessing image patterns of interest in each of the 2D image slices, it may be helpful to determine whether any of the 2D image patterns of interest belong to a larger high-dimensional structure, and if so, to combine the identified 2D image patterns into a higher-dimensional structure. This approach has several advantages, but in particular, by identifying high-dimensional structures across various slices/depths of the breast tissue, the end-user may be better informed as to the presence of a potentially significant structure that may not be easily visible in various 2D slices of the breast.
Further, instead of identifying similar image patterns in two 2D slices (that are perhaps adjacent to each other), and determining whether or not to highlight image data from one or both of the 2D slices, identifying both image patterns as belonging to the same high-dimensional structure may allow the system to make a more accurate assessment pertaining to the nature of the structure, and consequently provide significantly more valuable information to the end-user. Also, by identifying the high-dimensional structure, the structure can be more accurately depicted on the synthesized 2D image. Yet another advantage of identifying high-dimensional structures within the various captured 2D slices of the breast tissue relates to identifying a possible size/scope of the identified higher-dimensional structure. For example, once a structure has been identified, previously unremarkable image patterns that are somewhat proximate to the high-dimensional structure may now be identified as belonging to the same structure. This may provide the end-user with an indication that the high-dimensional structure is increasing in size/scope.
To this end, the hierarchical multi-level feature 2D synthesizer 104 creates, for a stack of image slices, a stack of object maps indicating possible locations of 3D objects. In other words, the stack of object maps depicts one or more probability regions that possibly contain high-dimensional objects. In some embodiments, the set of object maps may be used to create a high-dimensional object grid (e.g., a 3D object grid) comprising one or more high-dimensional structures (3D objects) present in the breast tissue. The stack of object maps represents a 3D volume representative of the patient's breast tissue, and identifies locations that probably hold identified 3D object(s).
However, creating object maps that identify probabilities associated with the presence of known high-dimensional objects is difficult because it may be difficult to ascertain whether a structure is an independent structure, or whether it belongs to a high-dimensional structure. Also, it may be computationally difficult and expensive to run complex algorithms to identify complicated image patterns contains in the various image slices, and identify certain image patterns as belonging to a known object. To this end, high-dimensional objects may be decomposed into lower-dimensional image patterns.
This may be achieved through a plurality of hierarchical multi-level feature modules that decompose high-dimensional objects into simpler low-level patterns. In other words, an image pattern constituting a high-level object representation can be decomposed into multiple features such as density, shape, morphology, margin, edge, line, etc. as will be described in further detail below. These decomposed representations may be computationally easier to process than the original high-level image pattern, and may help associate the lower-level image patterns as belonging to the higher-dimensional object. By decomposing more complex objects into simpler image patterns, the system enables easier detection of complex objects because it may be computationally easier to detect low-level features, while at the same time associating the low-level features to the high-dimensional object.
A high-dimensional object may refer to any object that comprises at least three or more dimensions (e.g., 3D object or higher, 3D object and time dimension, etc.). An image object may be defined as a certain type of image pattern that exists in the image data. The object may be a simple round object in a 3D space, and a corresponding flat round object in a 2D space. It can be an object with complex patterns and complex shapes, and it can be of any size or dimension. The concept of an object may extend past a locally bound geometrical object. Rather, the image object may refer to an abstract pattern or structure that can exist in any dimensional shape. It should be appreciated that this disclosure is not limited to 3D objects and/or structures, and may refer to even higher-dimensional structures. However, for simplicity, the remaining disclosure will refer to the higher-dimensional objects as 3D objects populated in a 3D grid.
The multi-level feature modules include a high-level feature module 114 to detect and identify higher-dimensional objects. For example, the high-level feature module 114 is configured to identify complex structures, such as a spiculated mass. However, it should be appreciated that the high-level feature module may require the most computational resources, and may require more complex algorithms that are programmed with a large number of filters or more computationally complex filters. Thus, in addition to directly utilizing a high-level feature module to recognize the complex structure, the 3D object may be decomposed into a range of mid-level and low-level features. Towards this end, the multi-level feature modules also include a mid-level feature module 112 configured to detect an image pattern of medium complexity, such as a center region of the spiculated mass, and a low-level feature module 110 configured to detect an even simpler image pattern, such as linear patterns radiating from the center of the spiculated mass.
Each of the multi-level feature modules (110, 112 and 114) may correspond to respective filters that comprise models, templates, and filters that enable each of the multi-level feature modules to identify respective image patterns. These multi-level feature modules are run on the input images (e.g., Tp, Tr, Mp, etc.) with their corresponding filters to identify the assigned high-level, mid-level and/or low-level features. Each hierarchical multi-level feature module (e.g., 110, 112 and 114) outputs a group of feature maps identifying areas of the respective image slice that comprise that particular feature. For example, the low-level feature module 110 may identify areas of the image slice that contains lines. The mid-level feature module 112 may identify areas of the image slice that contains circular shapes, and the high-level feature module 114 may identify areas containing the entire spiculated mass.
These feature maps outputted by the respective feature module may be combined using a combiner 120. The combiner 120 may be any kind of suitable combiner, e.g., a simple voting-based combiner such as shown in
The learning library-based combiner 120/122 stores a set of known shapes/image patterns, and uses the feature maps to determine a probability of whether a particular shape exists at a 3D location. Each object map 124 is formed based on combining the various feature maps derived through the feature modules. It should be appreciated that the formed object maps 124 may identify probabilities corresponding to multiple different objects, or may simply identify probabilities corresponding to a single object. In other words, a single object map 124 corresponding to a particular image slice may identify a possible location for two different objects. Or, a single object map 124 may identify two possible locations for the same object. Thus, multiple feature maps belonging to one or more high-dimensional objects may be combined into a single object map. The hierarchical multi-level feature synthesizer 104 utilizes the stack of object maps 124, in addition to the input images (e.g., Tr, Tp, Mp, etc.) in order to create one or more synthesized 2D images, as will be discussed in further detail below.
The synthesized 2D images may be viewed at a display system 105. The reconstruction engine 103 and 2D synthesizer 104 are preferably connected to a display system 105 via a fast transmission link. The display system 105 may be part of a standard acquisition workstation (e.g., of acquisition system 101), or of a standard (multi-display) review station (not shown) that is physically remote from the acquisition system 101. 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 105 of the system is preferably able to display respective Ms, Mp, 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.
Thus, the imaging and display system 100, which is described as for purposes of illustration and not limitation, is capable of receiving and selectively displaying tomosynthesis projection images Tp, tomosynthesis reconstruction images Tr, synthesized mammogram images Ms, and/or mammogram (including contrast mammogram) images Mp, or any one or sub combination of these image types. The system 100 employs software to convert (i.e., reconstruct) tomosynthesis images Tp into images Tr, software for synthesizing mammogram images Ms, software for decomposing 3D objects, software for creating feature maps and object maps. An object of interest or feature in a source image may be considered a ‘most relevant’ feature for inclusion in a 2D synthesized image based upon the application of the object maps along with one or more algorithms and/or heuristics, wherein the 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. The objects and features of interest may include, for example, spiculated lesions, calcifications, and the like.
As shown in the illustrated embodiment, the tomosynthesis stack 202 comprises a plurality of images 218 taken at various depths/cross-sections of the patient's breast tissue. Some of the images 218 in the tomosynthesis stack 202 comprise 2D image patterns. Thus, the tomosynthesis stack 202 comprises a large number of input images containing various image patterns within the images of the stack. For example, the tomosynthesis stack 202 may comprise one hundred images 218 captured at various depths/cross sections of the patient's breast tissue. Only a few of the images 218 may comprise any information of significance. Also, it should be noted that the tomosynthesis stack 202 simply contains 2D image patterns at various image slices 218, but it may be difficult to determine 3D structures based on the various cross-sectional images. However, the tomosynthesis stack 202 may be utilized in order to create the 3D breast volume 204 comprising the stack of object maps 124 (indicated by reference numbers 220a and 220b in
The 3D breast volume 204 may be considered a 3D coordinate space representing a patient's breast mass. Rather than depicting 2D image patterns at various image slices, the 3D breast volume 204 depicts, through the object maps 124 (220a, 220b), probable locations of identified 3D objects in the entire mass (or portion thereof) that represents the patient's breast tissue. The object maps 214 (220a, 220b) depict, for each image slice 218, a probability that a particular object (or objects) 222 is/are present at that particular coordinate location. Rather the simply display image patterns, the stack of object maps clearly identifies particular objects in the breast volume 204. This allows for more accurate rendering of the 2D synthesized image 206 that can depict locations of objects 222 rather than simply highlight interesting image patterns (that may or may not be related to objects). Knowing that image patterns belong to particular objects 222 provides the end-user with more insight when reviewing the synthesized 2D image 206.
The object maps 124 (220a, 220b) may comprise several areas depicting a probability that an object is present at that location. For example, in the illustrated embodiment, two object maps, 220a and 220b, are shown depicting probabilities for objects at two different locations. These may refer to a single object or multiple objects, as discussed above.
The object maps 220a and 220b are created by running the image slices 218 through the various hierarchical multi-level feature modules (e.g., modules 110, 112 and 114) to produce feature maps that are then combined together in consultation with the learning library-based combiner 120/122 to determine a possible location of the respective 3D object. It should be appreciated that each 3D object may correspond to respective high-level, mid-level and low-level feature modules. Each of the multi-level feature modules outputs feature maps that identify the particular feature in the image slice. Multiple feature maps may be combined using the learning-library-based combiner 120/122 to generate an object map 220a, 220b for a particular image slice 218.
For example, in the illustrated embodiment, object maps 220a and 220b may depict probabilities for two separate objects. Although not necessarily visible in the displayed object maps 220a, 220b, themselves, when these object maps 220a and 220b are viewed as a whole for the entire tomosynthesis stack 202, the shape/size and dimensions of the various objects will become clear in the 3D breast volume 204. Thus, since two objects 222 are identified in the 3D breast volume 204, the 2D synthesized image 206 identifies their locations. It should be appreciated, however, that these two identified objects 222 may be the same object or may be multiple objects. In particular, it should be appreciated that these objects 222 may be predefined objects that the system has been trained to identify. However, even in healthy breast tissue that does not necessarily comprise any suspicious objects or structures, the 3D breast volume 204 may display a breast background object. For example, all breast linear tissue and density tissue structures can be displayed as the breast background object. For example, the 3D object grid 204 may display a “breast background” pattern throughout the 3D grid, and one or more objects may be located at various areas of the breast background. In other embodiments, “healthy” objects such as spherical shapes, oval shapes, etc., may simply be identified through the 3D object grid 204. These identified 3D objects may then be displayed on the 2D synthesized image 206; of course, out of all identified 2D objects, more clinically-significant objects may be prioritized or otherwise enhanced when displaying the respective object on the 2D synthesized image, as will be discussed in further detail below.
In one or more embodiments, the hierarchical multi-level feature synthesizer 104 utilizes both the tomosynthesis image stack 202 along with the created 3D breast volume 204 containing the stack of object maps 220 in order to condense the relevant features into a single 2D synthesized image 206. As shown in the illustrated embodiment, the 2D synthesized image 206 provides important details from multiple image slices on a single 2D synthesized image 206. Simply utilizing legacy techniques on the tomosynthesis image stack 202 may or may not necessarily provide details about both identified objects. To explain, if there is overlap in the z direction of two important image patterns, the two image patterns are essentially competing with each other for highlighting in the 2D synthesized image. If it is not determined that the two image patterns belong to two separate objects, important aspects of both objects may be compromised. Alternatively, only one of the two structures may be highlighted at all in the 2D synthesized image 206. Or, in yet another scenario, the 2D synthesized image may depict both structures as one amorphous structure such that an important structure goes entirely undetected by the end-user.
Thus, identifying objects through the stack of object maps 220a, 220b, allows the system to depict the structures more accurately in the 2D synthesized image 206, and allows for various objects to be depicted simultaneously, even if there is an overlap of various objects in the coordinate space. Thus, utilizing the 3D breast volume 204 containing the stack of object maps 220a, 220b has many advantages in producing a more accurate 2D synthesized image 206.
In one or more embodiments, the tomosynthesis image stack 202 may be used to construct the 3D breast volume 204, as discussed above. The various images of the tomosynthesis image stack 202 may be run through the multi-level feature modules (e.g., modules 110, 112 and 114). More specifically, the tomosynthesis image stack 202 may be run through a high-level module 114 that is configured to identify complex structures. For example, the high-level module 114 corresponding to 3D spiculated masses may be configured to identify the entire spiculated lesion, or complex sub-portions of spiculated lesions. The high-level module 114 may be associated with high-level filters 212 that comprise models, templates and filters that allow the high-level feature module 114 to detect the assigned feature. Although the illustrated embodiment only depicts a single high-level, mid-level and low-level feature, it should be appreciated that there may be many more multi-level feature modules per object. For example, there may be separate high-level, mid-level and low-level modules for each of the two objects depicted in the 2D synthesized image 206.
The tomosynthesis image stack 202 may also be run through the mid-level feature module 112 that may be configured to identify mid-level features. For example, the mid-level feature module 112 corresponding to 3D spiculated masses may detect circular structures representative of the centers of spiculated lesions. The mid-level feature module 112 may be associated with mid-level filters 210 that comprise models, templates and filters that allow the mid-level module 112 to detect the assigned feature.
Similarly, the tomosynthesis image stack 202 may also be run through the low-level feature module 110 that may be configured to identify much simpler low-level features. For example, the low-level feature module 110 corresponding to 3D spiculated masses may detect lines representative of linear patterns that radiate from the centers of spiculated lesions. The low-level feature module 110 may be associated with low-level filters 208 that comprise models, templates and filters that allow the low-level module 110 to detect the assigned feature.
As will be described in further detail below, each of the multi-level feature modules outputs a feature map showing areas that contain the particular feature on the image slice. These outputted feature maps for each image slice 218 may be combined using the learning library-based combiner 120/122. The learning library-based combiner 120/122 may store a plurality of known objects and may determine, based on the outputted feature maps, a probability that a particular object is located on the image slice 218. It should be appreciated that the learning library 122 will achieve greater accuracy over time, and may produce increasingly more accurate results in identifying both the location, scope and identity of respective objects 222.
The learning library-based combiner 120/122 synthesizes information gained through the various feature maps outputted by each of the hierarchical multi-level feature modules, and combines the feature maps into the object maps 220a, 220b. As discussed above, the series of object maps 220a and 220b forms the 3D breast volume 204.
Referring now to
When the multi-level feature modules (e.g., 310, 312 and 314) are run on the stack of Tr slices 300a-300e, a set of feature maps 320a-320e are generated. In one or more embodiments, at least three groups of feature maps (for each of the three modules) are generated for each Tr image slice. More specifically, referring to feature maps 320a, feature map 410a is generated based upon running the low-level feature module 310 (that identifies linear patterns) on Tr slice 300a. Similarly, feature map 412a is generated based upon running the mid-level feature module 312 (that identifies circular patterns) on Tr slice 300a, and feature map 414a is generated based upon running the high-level feature module 314 (that identifies the spiculated lesion) on Tr slice 300a.
Similarly, feature maps 320b (comprising 410b, 412b, and 414b) are generated by running the multi-level feature modules 310, 312 and 314 on Tr slice 300b; feature maps 320c (comprising 410c, 412c, and 414c) are generated by running the multi-level feature modules 310, 312 and 314 on Tr slice 300c; feature maps 320d (comprising 410d, 412d, and 414d) are generated by running the multi-level feature modules 310, 312 and 314 on Tr slice 300d; and feature maps 320e (comprising 410e, 412e, and 414e) are generated by running the multi-level feature modules 310, 312 and 314 on Tr slice 300e. Although not drawn to scale, each of the feature maps represents a respective coordinate system that identifies regions of the image slice containing the assigned feature.
For example, referring to feature map 410a, a highlighted region 430 refers to the possibility of a linear structure being present at that coordinate location of the Tr slice 300a. Similarly, the highlighted region of feature map 412a indicates areas containing a circular structure in Tr slice 300a, and the highlighted region of feature map 414a indicates an area that possibly contains an entire spiculated lesion is present in Tr slice 300a. As can be seen from the range of feature maps, some highlighted regions are denser than other highlighted regions. For example, feature map 414c shows a highlighted region indicating a strong possibility that a spiculated lesion is detected. Similarly, other feature maps (e.g., 410b, 410c, 410d, etc.) illustrate multiple regions indicating several detected features at various locations. If no feature is detected at a particular Tr image slice, the respective feature maps may show no highlighted regions (e.g., 412e and 414e).
For example, edge filters may be used to detect edges in the image slice. Similarly, edge filters, line filters and shape filters may be used to detect linear patterns in the image slice 300c. Since the low-level module 310 is simply configured to detect linear patterns, these simple filters may be sufficient. When these filters are run on the image slice 300c, the feature map may record one or more regions that indicate a coordinate location of the line. Feature map 410c shows numerous regions of Tr slice 300c that comprise the low-level features (e.g., lines).
Similarly, the mid-level feature module 312 corresponds to the mid-level filters 210. In addition to (or instead of) the edge filters, gradient filters, line filters, and shape filters, the mid-level filter bank 210 may also comprise filters configured to recognize simple geometrical shapes. For example, the mid-level filters 210 may be configured to recognize a simple circular shape. In another embodiment, orthogonal direction filters may be configured that enable the system to determine whether an orthogonal direction of set of edges converge at a single center point. Such a combination of filters may be used to determine a region corresponding to a circular shape. The feature map 412c highlights regions comprising circular shapes present in image slice 300c.
The high-level feature module 314 corresponds to the high-level filters 212. In addition to (or instead of) filters described with respect to the low-level filters bank 208 and mid-level filters bank 210, the high-level filters 212 may comprise filters that are specifically trained to detect complex structures. These may be a combination of simple filters or more sophisticated image recognition algorithms that help detect a shape that most resembles a spiculated mass. It should be appreciated that these filters/algorithms may be computationally more complex as compared to the filters in the low-level and mid-level filters bank (e.g., 208 and 210 respectively). For example, in the illustrated embodiment, the high-level filters 208 may be configured to detect a complex geometrical shape, such as radiating lines around a circular shape. In the illustrated embodiment, the feature map 414c depicts regions of the image slice 300c containing the high-level feature. As discussed above, for each image slice, the feature maps corresponding to each of the multi-level feature modules (110, 112 and 114) are combined to form an object map depicting a probability that the particular object is present at a particular location of the image slice. The object maps are created using the learning library-based combiner 120/122, as discussed above.
The learning library-based combiner 120/122 may receive inputs from the three levels of feature maps regarding the presence of a spiculated mass. This pattern of information may help create an object map identifying a probability region 502 in the object map 420c. It should be appreciated that the technique described herein is simplified for illustrative purposes, and a number of complex machine learning algorithms may be used to accurately compute the probable location and dimensions of the 3D object. It should also be appreciated that machine learning algorithms employed as part of the learning library 122 may enable the system to detect and identify 3D objects using very little information as the system “learns” more over time. Thus, it is envisioned that the learning library 122 grows to be more efficient and accurate over time. For example, in one or more embodiments, weights may be assigned to feature maps derived through various feature modules in order for the system to gauge how much weight a particular feature module should be given. As the system “learns” more, the weights assigned to certain features may change.
As discussed above, the learning library-based combiner 120/122 combines information from the various feature maps in order to produce the object map 420c depicting the probability region 502 of a particular 3D object. For example, the probability region 502 may pertain to a location, size and scope of a spiculated mass that may be present in Tr image slice 300c. Similarly, the learning-library-based combiner 120/122 may output other object maps for the other image slices 300a, 300b, 300d and 300e (not shown). This stack of object maps may be used to create the 3D breast volume (such as 204 shown in
By contrast,
For example, filters associated with the high-level feature module, mid-level feature module and low-level feature module may be applied to each image of the Tr stack. At step 806, feature maps are generated by each hierarchical multi-level feature module (e.g., 3 feature maps are outputted assuming there are three multi-level feature modules associated with a particular 3D object. At step 808, the feature maps generated by the high-level feature module, mid-level feature module and the low-level feature module are combined to form an object map by using a learning library. The learning library utilizes the generated feature maps to determine a probability that the particular 3D object is located at a particular location of the Tr image slice. At step 810, multiple object maps corresponding to multiple Tr image slices are stacked to create a 3D breast volume. At step 812, a synthesized 2D image is created using the plurality of object maps in the 3D breast volume. At step 814, the synthesized 2D image is displayed to the end-user.
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. It will also be apparent to those skilled in the art that various changes and modifications may be made to the depicted and/or described embodiments (e.g., the dimensions of various parts), without departing from the scope of the disclosed inventions, which is to be defined only by the following claims and their equivalents. The specification and drawings are, accordingly, to be regarded in an illustrative rather than restrictive sense.
This application is a continuation application of U.S. patent application Ser. No. 16/497,764, filed Sep. 25, 2019, which application is a National Phase entry under 35 U.S.C. § 371 of International Patent Application No. PCT/US2018/024911, having an international filing date of Mar. 28, 2018, which claims the benefit under 35 U.S.C. § 119 to U.S. Provisional Patent Application Ser. No. 62/478,977, filed Mar. 30, 2017, the entire disclosures of which are hereby incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3502878 | Stewart | 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 |
4727565 | Ericson | Feb 1988 | 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. | Jun 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 et al. | 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 |
5660185 | Shmulewitz et al. | Aug 1997 | A |
5668889 | Hara | Sep 1997 | A |
5671288 | Wilhelm et al. | Sep 1997 | A |
5712890 | Spivey | 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 et al. | 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 |
7286634 | Sommer, Jr. et al. | Oct 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 | 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 | Apr 2010 | B2 |
7705830 | Westerman et al. | Apr 2010 | B2 |
7760924 | Ruth | 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 et al. | 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 |
11419565 | Gkanatsios | Aug 2022 | B2 |
11508340 | Kreeger | Nov 2022 | 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 | Claus | 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 |
20050113680 | Ikeda et al. | May 2005 | A1 |
20050113681 | DeFreitas et al. | 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 et al. | 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 |
20060274928 | Collins et al. | Dec 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 | Jan 2009 | A1 |
20090005668 | West et al. | Jan 2009 | A1 |
20090005693 | Brauner | Jan 2009 | A1 |
20090010384 | Jing et al. | Jan 2009 | A1 |
20090034684 | Bernard | 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 | May 2011 | A1 |
20110110570 | Bar-Shalev | May 2011 | A1 |
20110110576 | Kreeger | May 2011 | A1 |
20110125526 | Gustafson | 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 |
20120106698 | Karim | May 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 |
20140200433 | Choi | Jul 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 | 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 |
20220005277 | Chen | Jan 2022 | A1 |
20220013089 | Kreeger | Jan 2022 | A1 |
20220386969 | Smith | Dec 2022 | A1 |
20230053489 | Kreeger | Feb 2023 | A1 |
20230054121 | Chui | Feb 2023 | A1 |
20230056692 | Gkanatsios | Feb 2023 | A1 |
20230082494 | Chui | Mar 2023 | A1 |
20230125385 | Solis | Apr 2023 | A1 |
20230225821 | DeFreitas | Jul 2023 | A1 |
Number | Date | Country |
---|---|---|
2014339982 | Apr 2015 | AU |
1846622 | Oct 2006 | CN |
101066212 | Nov 2007 | CN |
202161328 | Mar 2012 | CN |
102429678 | May 2012 | CN |
107440730 | Dec 2017 | CN |
112561908 | Mar 2021 | 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 |
2004254742 | Sep 2004 | 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 |
2012-011255 | Jan 2012 | JP |
2012-501750 | 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 |
9005485 | May 1990 | WO |
9317620 | Sep 1993 | WO |
9406352 | Mar 1994 | WO |
199700649 | Jan 1997 | WO |
199816903 | Apr 1998 | WO |
0051484 | Sep 2000 | WO |
2003020114 | Mar 2003 | WO |
2005051197 | Jun 2005 | WO |
2005110230 | Nov 2005 | WO |
2005110230 | Nov 2005 | WO |
2005112767 | Dec 2005 | WO |
2005112767 | Dec 2005 | WO |
2006055830 | May 2006 | WO |
2006058160 | Jun 2006 | WO |
2007095330 | Aug 2007 | WO |
08014670 | Feb 2008 | WO |
2008047270 | Apr 2008 | WO |
2008054436 | May 2008 | WO |
2009026587 | Feb 2009 | WO |
2010028208 | Mar 2010 | WO |
2010059920 | May 2010 | WO |
2011008239 | Jan 2011 | WO |
2011043838 | Apr 2011 | WO |
2011065950 | Jun 2011 | WO |
2011073864 | Jun 2011 | WO |
2011091300 | Jul 2011 | WO |
2012001572 | Jan 2012 | WO |
2012068373 | May 2012 | 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 |
2014080215 | May 2014 | 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 |
2021021329 | Feb 2021 | WO |
Entry |
---|
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. |
“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. |
“Supersonic to feature Aixplorer Ultimate at ECR”, AuntiMinnie.com, 3 pages (Feb. 2018). |
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. |
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. |
Burbank, Fred, “Stereotactic Breast Biopsy: Its History, Its Present, and Its Future”, published in 1996 at the Southeastern Surgical Congress, 24 pages. |
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. |
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. |
Carton, AK, et al., “Dual-energy contrast-enhanced digital breast tomosynthesis—a feasibility study”, Br J Radiol. Apr. 2010;83 (988):344-50. |
Chan, Heang-Ping et al., “ROC Study of the effect of stereoscopic imaging on assessment of breast lesions,” Medical Physics, vol. 32, No. 4, Apr. 2005, 1001-1009. |
Chen, SC, et al., “Initial clinical experience with contrast-enhanced digital breast tomosynthesis”, Acad Radio. Feb. 2007 14(2):229-38. |
Diekmann, Felix., 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. |
Dromain, Clarisse et al., “Dual-energy contrast-enhanced digital mammography: initial clinical results”, European Radiology, Sep. 14, 2010, vol. 21, pp. 565-574. |
E. Shaw de Paredes et al., “Interventional Breast Procedure”, published Sep./Oct. 1998 in Curr Probl Diagn Radiol, pp. 138-184. (D15 in oppo). |
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). |
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. |
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. |
Freiherr, G., “Breast tomosynthesis trials show promise”, Diagnostic Imaging—San Francisco 2005, V27; N4:42-48. |
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. |
Ghiassi, M. et al., “A Dynamic Architecture for Artificial Networks”, Neurocomputing, vol. 63, Aug. 20, 2004, pp. 397-413. |
Giger et al. “Development of a smart workstation for use in mammography”, in Proceedings of SPIE, vol. 1445 (1991), pp. 101103; 4 pages. |
Giger et al., “An Intelligent Workstation for Computer-aided Diagnosis”, in RadioGraphics, May 1993, 13:3 pp. 647-656; 10 pages. |
Hologic, “Lorad StereoLoc II” Operator's Manual 9-500-0261, Rev. 005, 2004, 78 pgs. |
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. |
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. |
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. |
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. |
Lewin,JM, et al., Dual-energy contrast-enhanced digital subtraction mammography: feasibility. Radiology 2003; 229:261-268. |
Lilja, Mikko, “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. |
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. |
Pathmanathan et al., “Predicting tumour location by simulating large deformations of the breast using a 3D finite element model and nonlinear elasticity”, Medical Image Computing and Computer-Assisted Intervention, pp. 217-224, vol. 3217 (2004). |
PCT International Preliminary Report on Patentability in International Application PCT/US2018/024911, dated Oct. 10, 2019, 8 pages. |
PCT International Search Report and Written Opinion in International Application PCT/US2018/024911, dated Jul. 2, 2018, 10 pages. |
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. |
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. |
Reynolds, April, “Stereotactic Breast Biopsy: A Review”, Radiologic Technology, vol. 80, No. 5, Jun. 1, 2009, pp. 447M-464M, XP055790574. |
Sakic et al., “Mammogram synthesis using a 3D simulation. I. breast tissue model and image acquisition simulation” Medical Physics. 29, pp. 2131-2139 (2002). |
Samani, A. et al., “Biomechanical 3-D Finite Element Modeling of the Human Breast Using MRI Data”, 2001, IEEE Transactions on Medical Imaging, vol. 20, No. 4, pp. 271-279. |
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. |
Smith, A., “Full field breast tomosynthesis”, Radiol Manage. Sep.-Oct. 2005; 27(5):25-31. |
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. |
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. |
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. |
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). |
Yin, H.M., et al., “Image Parser: a tool for finite element generation from three-dimensional medical images”, BioMedical Engineering Online. 3:31, pp. 1-9, Oct. 1, 2004. |
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. |
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 Cancer”, 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. |
Duan, Xiaoman et al., “Matching corresponding regions of interest on cranio-caudal and medio-lateral oblique view mammograms”, IEEE Access, vol. 7, Mar. 25, 2019, pp. 31586-31597, XP011715754, DOI: 10.1109/Access.2019.2902854, retrieved on Mar. 20, 2019, abstract. |
Samulski, Maurice et al., “Optimizing case-based detection performance in a multiview CAD system for mammography”, IEEE Transactions on Medical Imaging, vol. 30, No. 4, Apr. 1, 2011, pp. 1001-1009, XP011352387, ISSN: 0278-0062, DOI: 10.1109/TMI.2011.2105886, abstract. |
Nikunjc, Oza et al., Dietterich, T.G., Ed., “Ensemble methods in machine learning”, Jan. 1, 2005, Multiple Classifier Systems, Lecture Notes in Computer Science; LNCS, Springer-Verlag Berlin/Heidelberg, pp. 1-15, abstract. |
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20220192615 A1 | Jun 2022 | US |
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Child | 17692989 | US |