1. Field of the Invention
The present invention relates generally to a device, system and method for performing surgical soft tissue lesion excision, more specifically, to a device, system and method for surgical soft tissue lesion excision performed after radiologic localization of the tissue lesion to be excised.
2. Description of the Related Art
In current practice, a patient with a radiologically identified lesion, for example, a breast lesion, which cannot be palpated by a physician, and thus cannot be surgically removed without some sort of guide or marker, is marked by placement of a radiologically guided wire which is placed into the tissue of the radiologically identified lesion. Subsequently, a surgeon during an operation, makes an incision and follows the guide wire down to the lesion, then excises the lesion. There are a number of inherent problems with this procedure as currently practiced. The first is that the currently available guide wires are easily dislodged from the lesion during manipulation during the operation. Second, the guide wire, as currently used, marks only the approximate center of the lesion. As the lesion is surrounded by tissue, and often not palpable by the surgeon's fingers, thus, the lesion can be inadvertently cut into, incompletely removed, or missed altogether. There is substantial need in the field for a radiologically guided marker which also surrounds and encompasses the lesion to be excised, preventing dislodging, cutting into the lesion, incompletely removing the lesion, or missing the lesion altogether.
In preferred embodiments, the present invention comprises a radiologically placed soft tissue lesion excision device and system used to mark, encompass, and provide tactile feedback to the surgeon during the surgical removal of a soft tissue lesion.
In some embodiments, the device and system comprise a soft tissue encompassing element, an insertion element, a deployment element and a removal element. The soft tissue encompassing element comprises three or more shape memory wires, preferably formed from nitinol, or any other shape memory material. Each wire being formed such that it has a straight proximal section and a curved distal section, the curved distal section being pre bent in a generally curvilinear configuration and having the ability to be straightened fully, and then return to its original curvilinear configuration. The three or more shape memory wires are formed into a fixed arrangement such that the straight portions of the wires are generally parallel to and fixed to one another at a proximal end, forming a central axis, and the planes described by the curvilinear portions of the wires each being generally parallel to one another, perpendicular to the central axis, and spaced radially equidistant from one another.
For example, in a device comprising three wires, the curved portion of each wire would describe a vertical plane generally perpendicular to the central axis formed by the fixed straight portion of the wire. The planes described by the curved portions of the three wires would each be generally parallel to one another and spaced approximately one hundred and twenty degrees from one another. If four wires are used the planes described by the curved portions of the four wires would each be approximately ninety degrees from one another. The central straight portions of the wires being fixed to one another, or to a fixation element, such that the wires maintain their planar orientation rigidly. In a preferred embodiment, an extension wire is fixed to the proximal end of the three or more shape memory wires, or to the fixation element and is configured to extend outward through the skin of a patient and functional to act as a guide for the surgeon to locate the distal end of the encompassing element during an operation. In another embodiment, the extension wire is absent and the three or more shape memory wires are of a length that they can extend out from the lesion past the skin of a patient and act as a guide for the surgeon to locate the distal end of the encompassing element during an operation.
An insertion element comprises a hollow tube with an inner diameter large enough to admit the soft tissue encompassing element within said inner diameter, and sharp or beveled at one end to allow it to penetrate the tissue through which it is to be inserted. In another embodiment there is an infusion port connected to the inner channel of the hollow tube which may be used to administer a local anesthetic agent prior to deployment of the encompassing element. In another embodiment there are perforations in the distal end of the hollow tube functional to allow the infused liquid into the tissue lateral to the soft tissue lesion.
A deployment element comprises a second hollow tube, with an outer diameter small enough to fit inside the inner diameter of the insertion element and with an inner diameter both large enough to admit the extension wire of the encompassing element and small enough to prevent the three or more shape memory wires from passing through it. At a proximal end is a flattened portion functional to be pressed upon by a physician's finger.
A removal element comprises a hollow tube with an inner diameter large enough to admit the soft tissue encompassing element within said inner diameter, and with a conical bevel at one end configured to guide the curvilinear portions of the encompassing element into the inner diameter of the removal element allowing the encompassing element to be removed from the soft tissue lesion it has been inserted into following surgical excision of the lesion.
In a first stored configuration, the encompassing element is inserted into the inner diameter of the insertion element with the curvilinear portions of the shape memory wires having a generally straight configuration. The deployment element is inserted into the proximal end of the inner diameter of the insertion element such that the extension wire resides inside the inner diameter of the deployment element and the distal tip of the deployment element abuts the proximal ends of the three or more shape memory wires. In this configuration, the apparatus may be placed through the skin of a patient and into the approximate center of the soft tissue lesion, preferably via radiologic guidance. Once located into the approximate center of the lesion, the deployment element is pushed into the insertion element, deploying the encompassing element outward through the sharpened tip of the insertion element. As the encompassing element is deployed, the tips of the curvilinear portions of the shape memory wires penetrate the tissue and while traveling through the tissue, resume their curvilinear configuration surrounding and encompassing the soft tissue lesion. Once fully deployed, the insertion element and deployment element are withdrawn from the tissue, leaving the encompassing element in place around the tissue and the extension wire exiting from and extending outwardly past the surface of the skin. The patient would then be taken to an operating room and a surgeon would make an incision in the skin, then follow the extension wire down to the encompassing element surrounding the lesion. The surgeon would then excise the lesion encompassed within the encompassing element by cutting along the outer diameter formed by the shape memory wires in their curvilinear configuration surrounding the lesion. Once the lesion has been excised, the removal element is slid down the proximal portion of the encompassing element and the encompassing element pulled into the inner diameter of the removal element, removing the encompassing element from the soft tissue lesion allowing for pathological analysis of the lesion.
The present invention will be readily understood by the following detailed description in conjunction with the accompanying drawings, wherein like reference numerals designate like structural elements, and in which:
The following description is provided to enable any person skilled in the art to make and use the invention and sets forth the best modes contemplated by the inventor for carrying out the invention. Various modifications, however, will remain readily apparent to those skilled in the art. Any and all such modifications, equivalents and alternatives are intended to fall within the spirit and scope of the present invention. In describing the orientation of the device, the term proximal will refer to that end of the described part closest to the portion.
An insertion element 30 comprises a hollow tube having an outer wall 31 and an inner channel 32. The insertion element is preferably sharpened at one end 33 with the diameter of the inner channel 32 being large enough to admit the full diameter of the soft tissue encompassing element 20.
As illustrated in
In preferred embodiments, a deployment element 40 comprises a second hollow tube, having an outer wall 41 and an inner channel 42 and a widened plunger 43 on its proximal end. The deployment element being formed such that the diameter of the outer wall 41 is smaller than the inner diameter of the channel 32 of the insertion element 30 and functional to slide easily inside the inner channel 32 of the insertion element 30. The inner channel of the deployment element 42 is formed such that it is larger than the diameter of the extension wire 22 but smaller than the diameter of the shelf 23 formed by the combination of the proximal ends of the three or more shape memory wires 21 allowing the distal end of the deployment element to abut said shelf 23 of the shape memory wires 22 and functional to slide the marking and encompassing element distally into the tissue when pressure is applied to the plunger 43.
Once fully deployed, the insertion element 30 and deployment element 40 are withdrawn from the tissue, leaving the encompassing element 20 in place around the soft tissue lesion 60 and the extension wire 22 extending outwardly past the surface of and exiting from the skin of the patient. The patient would then be taken to an operating room and a surgeon would make an incision in the skin, then follow the extension wire 22 down to the encompassing element 20 surrounding the lesion 50. The surgeon would then be able to safely excise the lesion encompassed within the encompassing element by cutting around the outer diameter formed by the shape memory wires 21 in their curvilinear configuration surrounding the lesion 60. Following excision of the soft tissue lesion 60 the encompassing element 20 may be removed from the soft tissue lesion 60 by sliding the removal element 50 down over first the extension wire 22 then over the proximal straight portion of the encompassing element 211. The encompassing element 20 is then drawn up into first the flared conical end 53 of the removal element 50 and then into the inner channel of the removal element 52, the flared conical end functional to guide the curvilinear portions of the shape memory wires 212 into a more straightened configuration, facilitating the entry of the curvilinear portions of the shape memory wires 212 into the inner channel 52.
Those skilled in the art will appreciate that various adaptations and modifications of the just described preferred embodiments can be configured without departing from the scope and spirit of the invention. Therefore, it is to be understood that, within the scope of the appended claims, the invention may be practiced other than as specifically described herein.
This application claims the benefit of U.S. Provisional Application No. 61/869,825, filed Aug. 26, 2013, entitled SOFT TISSUE LESION EXCISION GUIDE, the disclosure of which is herein incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61869825 | Aug 2013 | US |