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Claims  |
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What is claimed is:
1. Apparatus for positioning a tip of a biopsy device for insertion into a selected region of a tissue mass, the apparatus for use in a system including display means, the
apparatus comprising:
an ultrasonic scanner that provides an image of the tissue mass, the image of the tissue mass, including the selected region, displayed on the display means;
a support for holding a tip of a biopsy device with a trajectory;
means, other than the ultrasonic scanner, coupled to the support for generating a signal corresponding to a current location of the tip of the biopsy device, prior to insertion into the tissue mass, the signal being displayed on the display means
by a symbol representative of the current location of the tip of the biopsy device relative to the selected region,
wherein aligning the symbol with the selected region corresponds to moving the support to position at which the trajectory of the tip of the biopsy device will intersect the selected region.
2. The apparatus as defined in claim 1 wherein the support comprises first and second support tracks disposed in orthogonal relation to one another.
3. The apparatus as defined in claim 1 wherein the means for generating a signal comprises at least one encoder.
4. The apparatus as defined in claim 1 wherein the ultrasonic scanner provides real-time imaging of the tissue mass.
5. The apparatus as defined in claim 4 wherein the ultrasonic scanner provides imaging of the tip of the biopsy device after the tip of the biopsy device has been inserted into the tissue mass.
6. The apparatus as defined in claim 1 wherein the support releasably holds the biopsy device, so that the biopsy device may be released from the support after insertion of the tip of the biopsy device into the tissue mass to enable free-hand
manipulation of the biopsy device.
7. The apparatus as defined in claim 1 wherein the ultrasonic scanner forms a first compression surface, the apparatus further comprising a tissue support table forming a second compression surface, the tissue mass immobilized between the first
and second compression surfaces.
8. The apparatus as defined in claim 2 further comprising a tissue support table, the first support track removably anchored to the tissue support table.
9. The apparatus as defined in claim 2 further comprising a dummy X-ray film cassette, the first support track anchored to the dummy X-ray film cassette.
10. The apparatus as defined in claim 1 wherein the ultrasonic scanner comprises an ultrasonic transducer and a compression plate having an edge, the ultrasonic transducer disposed at an angle relative to the compression plate so that the
ultrasonic transducer provides imaging of regions of the tissue mass located near, or extending beyond, the edge of the compression plate.
11. The apparatus as defined in claim 1 wherein the ultrasonic scanner comprises an ultrasonic transducer and a compression plate having an edge, the ultrasonic transducer and the compression plate disposed at an angle relative to a horizontal
plane so that the ultrasonic transducer provides imaging of regions of the tissue mass located near, or extending beyond, the edge of the compression plate.
12. The apparatus as defined in claim 1 wherein the display means displays images of the tissue mass from a selected one of a plurality of orthogonal views.
13. Apparatus for positioning a tip of a biopsy device for insertion into a selected region of a tissue mass, the apparatus for use in a system including display means and an ultrasonic scanner that provides an image of the tissue mass, the
apparatus comprising:
a support for holding a tip of a biopsy device with a trajectory;
means, other than the ultrasonic scanners, coupled to the support for generating a signal corresponding to a current location of the tip of the biopsy device, prior to insertion into the tissue mass,
the display means displaying the image of the tissue mass including the selected region and a symbol representative of the current location of the tip of the biopsy device relative to the selected region, so that aligning the symbol with the
selected region corresponds to moving the support to position at which the trajectory of the tip of the biopsy device will intersect the selected region.
14. The apparatus as defined in claim 13 wherein the support comprises first and second support tracks disposed in orthogonal relation to one another.
15. The apparatus as defined in claim 13 wherein the means for generating a signal comprises at least one encoder.
16. A system including the apparatus as defined in claim 13, wherein the ultrasonic scanner provides real-time imaging of the tissue mass.
17. The system as defined in claim 16 wherein the ultrasonic scanner provides imaging of the tip of the biopsy device after the tip of the biopsy device has been inserted into the tissue mass.
18. The apparatus as defined in claim 13 wherein the support releasably holds the biopsy device, so that the biopsy device may be released from the support after insertion of the tip of the biopsy device into the tissue mass to enable free-hand
manipulation of the biopsy device.
19. A system including the apparatus as defined in claim 13, wherein the ultrasonic scanner forms a first compression surface, the system further comprising a tissue support table forming a second compression surface, the tissue mass immobilized
between the first and second compression surfaces.
20. The apparatus as defined in claim 14 further comprising a tissue support table, the first support track removably anchored to the tissue support table.
21. The apparatus as defined in claim 14 further comprising a dummy X-ray film cassette, the first support track anchored to the dummy X-ray film cassette.
22. A system including the apparatus as defined in claim 13, wherein the ultrasonic scanner comprises an ultrasonic transducer and a compression plate having an edge, the ultrasonic transducer disposed at an angle relative to the compression
plate so that the ultrasonic transducer provides imaging of regions of the tissue mass located near, or extending beyond, the edge of the compression plate.
23. A system including the apparatus as defined in claim 13, wherein the ultrasonic scanner comprises an ultrasonic transducer and a compression plate having an edge, the ultrasonic transducer and the compression plate disposed at an angle
relative to a horizontal plane, so that the ultrasonic transducer provides imaging of regions of the tissue mass located near, or extending beyond, the edge of the compression plate.
24. A system including the apparatus as defined in claim 13, wherein the display means displays images of the tissue mass from a selected one of a plurality of orthogonal views.
25. A method of positioning a tip of a biopsy device to have a predetermined trajectory into a selected region of a tissue mass, the method comprising steps of:
immobilizing the tissue mass;
generating an ultrasonic image of the tissue mass including the selected region;
displaying the ultrasonic image of the tissue mass including the selected region;
providing a support for holding a tip of a biopsy device with a trajectory;
generating a signal corresponding to a current location of the tip of the biopsy device, prior to insertion of the tip of the biopsy device into the tissue mass;
displaying a symbol representative of the current location of the tip of the biopsy device relative to the selected region, responsive to the signal; and
moving the support to a location at which the symbol is aligned with the selected region, so that the trajectory of the tip of the biopsy device will intersect the selected region.
26. The method as defined in claim 25 further comprising a step of providing a real-time ultrasonic image of the tissue mass.
27. The method as defined in claim 26 further comprising steps of:
inserting the tip of the biopsy device into the tissue mass while providing a real-time ultrasonic image of the tissue mass and the tip of the biopsy device;
displaying the ultrasonic image of the tissue mass and the tip of the biopsy device; and
guiding insertion of the tip of the biopsy device into the tissue mass responsive to the displayed image.
28. The method as defined in claim 25 further comprising steps of:
releasing the biopsy device from the support after insertion of the tip of the biopsy device into the tissue mass; and
manipulating the biopsy device free-hand to alter the trajectory of the tip of the biopsy device within the tissue mass.
29. The method of claim 25 wherein the step of displaying the ultrasonic image of the tissue mass comprises displaying an elevation view of the tissue mass.
30. The method of claim 27 wherein the step of displaying an ultrasonic image of the tissue mass and the tip of the biopsy device comprises displaying a plan view of the tissue mass and tip of the biopsy device. |
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Claims  |
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Description  |
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FIELD OF THE INVENTION
The present invention relates to apparatus and methods for performing biopsy of biological tissue, and more particularly, to performing biopsy of biological tissue guided by ultrasound imaging.
BACKGROUND OF THE INVENTION
Apparatus and methods are known to identify tumorous masses suspected of being malignant, for example, by radiographic and sonographic techniques. It is typical for such tissue masses to then be biopsied to determine status as, or degree of,
malignancy, to determine further course of treatment. For example, a region of a mammogram suspected to contain a lesion may be biopsied to determine whether the lesion is benign or malignant, and if malignant, the course of treatment appropriate for
the degree of malignancy, e.g. mastectomy, radiation treatment or chemotherapy.
Previously known biopsy methods range from minimally invasive techniques, such as fine needle aspiration using a 21 gauge hypodermic needle and large core biopsy using a 14 gauge needle mounted in an automated biopsy gun, to open-procedures in
which the lesion is surgically excised. Minimally invasive techniques are faster, less expensive, safer and less traumatic for the patient than surgical excision, and begun developing widespread acceptance.
A concern common to previously known minimally invasive biopsy techniques, however, is ensuring that the biopsy needle actually obtains a tissue sample from the suspected lesion, rather than adjacent healthy tissue. Previously known techniques
that attempt to ensure that the biopsy needle trajectory enters the region of the suspected lesion are described, for example, in Fornage et al., "Ultrasound-Guided Needle Biopsy Of The Breast And Other Interventional Procedures," Radiologic Clinics Of
North America, Vol. 30, No. 1 (January 1992), Fornage et al. "Breast Masses: US-Guided Fine Needle Aspiration Biopsy," Radiology, 162:409-414 (February 1987), Parker et al., "US-guided Automated Large-Core Breast Biopsy," Radiology, 187:507-511 (May
1993), and Parker and Jobe, "Large-Core Breast Biopsy Offers Reliable Diagnosis," reprinted from Diagnostic Imaging (October 1990).
The foregoing articles describe a free-hand ultrasound technique, in which insertion of a biopsy needle into a suspected lesion is performed by holding a linear array ultrasound transducer in one hand and inserting the needle into the tissue with
the other hand. In particular, the ultrasound transducer is held above the midline of the suspicious mass and the needle (or needle of the automated biopsy gun) is then inserted in the tissue near the base of the transducer, so that the tip of the
needle appears in the ultrasound scan. In addition, when a biopsy gun is employed, additional personnel may be required to steady the biopsy gun during use or to hold the ultrasound transducer.
As described in the Fornage et al. articles and Parker et al. article, difficulties arise using the free-hand technique where the suspected lesion is located near the patient's chest wall, or in proximity to a prothesis. These articles also
emphasize that the practitioner's level of skill in using the free-hand technique can dramatically influence the results obtained. All of the foregoing articles reject the use of biopsy needle guides that can be attached to the ultrasound transducer,
because the guides interfere with the flexibility and maneuverability required to obtain satisfactory results.
The Parker and Jobe article also describes stereotactic mammographic biopsy systems. In such systems, two X-ray images of the breast tissue are made at different angles, thereby permitting the coordinates of a lesion to be calculated. The
biopsy needle, typically an automated biopsy gun (e.g., Biopty from C. R. Bard, Inc., Bard Urological Division, Covington, Ga.) mounted in a rigid housing attached to the biopsy table, is moved to the calculated coordinates and actuated. Two additional
X-ray views of the breast tissue are then taken to confirm that the needle has actually sampled the region of the suspected lesion.
The Parker and Jobe article further describes the drawbacks of add-on stereotactic systems--namely, the potential for breast movement that renders earlier stereo calculations worthless. That article also describes the Mammotest system sold by
Fischer Imaging Corporation, Thornton, Colo., as overcoming some of the problems of add-on stereotactic systems, but at a considerable cost differential.
A drawback common to all of the stereotactic systems, however, is the need for multiple X-rays of the tissue, thus exposing the tissue to potentially unhealthful ionizing radiation. These systems also provide no real-time imaging of the needle
trajectory, so as described in the Parker and Jobe article, intervening movement of the breast tissue may render the calculated coordinates useless and result in a potentially misleading biopsy sample. Indeed, the clinician is not even aware that the
biopsy needle missed the intended target until after the follow-up stereotactic views are taken.
Moreover, because the biopsy needle is secured in a fixed housing so as to provide a fixed trajectory for biopsy needle, stereotactic systems provide no freedom of movement for the biopsy needle relative to the target tissue. Consequently,
several needle insertions and withdrawals are required to adequately characterize the tissue.
A major disadvantage of the above-described previously known methods and apparatus arises due to the inability of the clinician to estimate, in real-time, the correct trajectory of the biopsy needle from the breast surface to the region of the
suspected tumor or lesion. Even when guided by free-hand ultrasound scanning, the clinician typically must insert and withdraw the biopsy needle ten to fifteen times or more to improve the confidence level that a portion of the suspected lesion has been
collected. Then, each of the needle aspiration samples must be separately tested, significantly increasing the overall cost of the procedure.
Likewise, in stereotactic systems, the inability to monitor tissue movement and to manipulate the biopsy needle once inserted, creates the need for multiple needle insertions to obtain adequate characterization of the suspected lesion. And
again, each of these multiple samples must be individually tested to properly characterize the suspected lesion.
Such repetitive insertion and withdrawal of the biopsy needle may cause significant patient discomfort. Moreover, in those cases where the biopsy indicates no need for treatment by surgical methods, the repeated biopsy needle insertion may
nevertheless leave the patient with cosmetically unappealing scar tissue.
A further disadvantage of these previously known methods and apparatus is the potential for seeding the needle tracks with potentially malignant tumor cells. For example, because the clinician in previously known methods must make several needle
insertions to confirm that he or she has sampled cells from the target tissue, there is the potential that malignant cells may be dispersed along a needle track which was not believed by the clinician to have entered the region of the suspected tumor,
but which in fact did so.
In view of the foregoing, it would be desirable to provide apparatus and methods by which a biopsy needle could be positioned for insertion so as to have a real-time, predetermined trajectory to a targeted tissue region, thereby reducing the need
for repetitive needle insertion and withdrawal to obtain a biopsy sample.
It would also be desirable to provide apparatus and methods by which a biopsy needle could be positioned for insertion in real-time with a high degree of confidence that the needle trajectory will enter a targeted tissue region, thus reducing the
risk of spreading potential malignant tumor cells by dispersing them along multiple needle tracks.
It would also be desirable to provide apparatus and methods by which a biopsy needle could be positioned for insertion into tissue along a predetermined trajectory, and which enables the clinician to alter that trajectory once the needle has been
inserted, so as to reduce the number of scars resulting from repetitive skin punctures.
A yet further drawback of previously known biopsy systems, including those employing ultrasonic imaging of the biological tissue, is the inability to assess tissue features located near, or extending within, the chest wall. Such features
typically have been inaccessible to previously known radiographic and sonographic imaging techniques due to the inability, for example, to direct such X-radiation to the X-ray film, while in sonographic systems, complicated structures including
submersing the tissue in a water bath have been required.
It therefore would be desirable to provide a biopsy system having enhanced imaging capability to provide images of biological features located near or within a patient's chest line.
SUMMARY OF THE INVENTION
In view of the foregoing, it is an object of this invention to provide a apparatus and methods by which a biopsy needle may be initially positioned in real-time for insertion so as to have a predetermined trajectory to a targeted tissue region.
In this manner, the need for repetitive needle insertion and withdrawal to obtain a biopsy sample is reduced, improving the efficiency of the medical procedure, and reducing patient distress during the medical procedure.
It is another object of this invention to provide apparatus and methods by which a biopsy needle may be positioned for insertion in real-time with a high degree of confidence that the needle trajectory will enter a targeted tissue region, thereby
reducing the risk of spreading potential malignant tumor cells by dispersing them along multiple needle tracks.
It is yet another object of the present invention to provide apparatus and methods by which a biopsy needle may be positioned for insertion into tissue along a predetermined trajectory, and which enables the clinician to alter the needle
trajectory once the needle has been inserted, thus reducing the number of scars resulting from repetitive skin punctures as well as patient discomfort.
It is yet a further object of this invention to provide apparatus and methods by which a clinician can image biological features within tissue that are located near, or extend within, a patient's chest wall, thereby enabling more thorough
examination of the tissue and more thorough biopsy, if indicated.
These and other objects of the invention are accomplished in accordance with the principles of the invention by providing apparatus and methods in which a biopsy needle is guided to an initial insertion position by correlating, in real-time, the
actual needle position prior to insertion with its probable trajectory once inserted. In a preferred embodiment, the needle location is tracked electronically and projected over a previously stored or real-time image of the tissue. The clinician may
then observe which features of the imaged tissue the biopsy needle is likely to intersect when inserted. Additionally, ultrasound scanning of a selected trajectory may also be provided to assess depth of penetration of the biopsy needle, when inserted.
The ultrasound scanning provided by the apparatus of the present invention may include the capability, by angling either the ultrasound transducer or the upper compression plate relative to the chest wall, to provide imaging of biological
features located near, or extending within, the chest line.
Further features of the invention, its nature and various advantages will be more apparent from the accompanying drawings and the following detailed description of the preferred embodiments.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a perspective view of an illustrative embodiment of the biopsy system of the present invention;
FIG. 2 is an exploded perspective enlarged view of a portion of the biopsy system of FIG. 1, indicated in inset 2 of FIG. 1;
FIGS. 3A-3C are perspective and elevational views, respectively, of an alternative needle support assembly in the open and closed positions;
FIG. 4 is a perspective view from beneath of an alternative arrangement of the biopsy system of FIGS. 1 and 2;
FIG. 5 is a perspective view of compressed breast tissue showing the reference axes employed with the biopsy system of the present invention;
FIG. 6 is an illustrative Y-Z display of the compressed breast tissue of FIG. 5, taken along line 6--6 of FIG. 5;
FIG. 7 is an illustrative X-Y display of the compressed breast tissue of FIG. 5, taken along line 7--7 of FIG. 5, showing a biopsy needle partially inserted into the tissue;
FIG. 8 is a cross-sectional view of an ultrasound scanning system constructed in accordance with the present invention that enables imaging of biological features located near, or extending within, the patient's chest line;
FIG. 9 is a cross-sectional view of an alternative embodiment of the system of FIG. 8.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to a system for performing biopsy of biological tissue, as indicated by, for example, a sonogram or mammogram. In overview, the apparatus of the present invention uses a previously stored or real-time ultrasound
image to determine an initial position for a biopsy needle so that there is a high degree of confidence that the needle trajectory will intersect a target tissue region, for example, a suspected lesion.
In a first illustrative embodiment described herein, the biopsy system includes stand-alone sonography apparatus. In an alternative embodiment, the biopsy system may be used in conjunction with a sonomammography system as described in copending,
commonly assigned patent application Ser. No. 08/277,894, filed Jul. 20, 1994, which is incorporated by reference herein in its entirety.
Referring now to FIG. 1, biopsy system 10 constructed in accordance with the principles of the present invention is described. System 10 comprises biopsy table 11 and computer-based display system 12. Biopsy table 11 includes ultrasonic scanner
13, tissue support table 14, and needle support system 15 movably mounted on support members 16 between base 17 and top block 18. Biopsy needle 19 is releasably carried by needle support system 15, as described in detail hereinafter. Needle support
system 15 is detachably coupled to computer 20 of computer-based display system 12 by cable 21, so that movement of biopsy needle is displayed by monitor 23 of computer-based display system 12.
Ultrasonic scanner 13 may be constructed as described with respect to FIG. 7 of the above-incorporated U.S. patent application Ser. No. 08/277,894, so as to include an annular or linear array ultrasonic transducer mounted for movement in an X-Y
plane as indicated by the axes shown in FIG. 1 herein. In particular, the ultrasound transducer may be mounted on a carriage that is driven by a system of belts, cables, drive screws, or similar mechanisms to provide scanning along a series of planes
sufficient to generate a three-dimensional data model of the tissue to be biopsied.
Ultrasonic scanner 13 includes a lower surface that functions as an upper compression plate, for immobilizing tissue against tissue support table 14. While the compression plate of ultrasonic scanner 13 may be constructed of any of the materials
described in the above-incorporated application, it will of course be understood that radiolucency of the compression plate is not required for stand-alone sonographic applications of the present invention. Ultrasonic scanner 13 may also incorporate
certain improvements, described in detail hereinafter, that enable imaging of biological features located near, or within, the patient's chest line. Imaging data generated by ultrasonic scanner is provided to computer-based display system 12 via cable
22.
Tissue support table 14 of the illustrative embodiment of FIG. 1 comprises a sturdy material, e.g., metal, fiberglass or plastic, such as UHMW plastic (e.g., ultra high molecular weight polyethylene), or combinations thereof, and serves to
support the lower surface of the biological tissue in compression. In particular, tissue support table 14 and ultrasonic scanner 13 may be releasably and adjustably mounted to support members 16 to provide both adequate compression of the tissue and to
provide height adjustment to accommodate the size of the patient.
Computer-based display system 12 is illustratively shown comprising monitor 23 and computer 20 disposed on movable cart 24. Computer 20 may be a general purpose personal computer, having for example, an 80386 or greater microprocessor, or
similar processor, and a hard disk drive, or similar memory device sufficient for storing software programs, to manipulate imaging data generated by ultrasonic scanner 13 and positioning data generated by needle support system 15. As will of course be
understood, system 12 includes one or more additional cards for processing data received from ultrasonic transducer 13 and needle support system 15, the implementation details of which employ routine application of ultrasound signal acquisition
principles, and which therefore form no part of the present invention.
Referring now to FIG. 2, an illustrative embodiment of needle support system 15 is described. Needle support system 15 includes anchor bar 25, support block assemblies 26 and 27, Y-axis track 28, Y-axis linear encoder 29, support plate assembly
30, Z-axis track 31, Z-axis linear encoder 32, and needle support block assembly 33.
Anchor block 25 is dimensioned to fit with close tolerances into grooves 34 provided in the lateral sides of tissue support table 14. Positioning holes 35 are provided in the grooved portion of tissue support table 14 so that locking pegs (not
shown) can be extended through holes 35 and into holes 36 of anchor block 25, thus positively locking anchor block 25 (and thus needle support system 15) into known relation with tissue support table 14.
The combination of groove 34 and anchor block 25 provides a high degree of rigidity to the overall needle support system, while provision of grooves 34 on each side of tissue support table 14 enables the clinician to obtain access to the tissue
from either the left or right side. In addition, ultrasonic scanner 13 and tissue support table 14 may be adjustably mounted, for example, to a block that is in turn pivotally connected to support members 16, so as to enable the entire biopsy system to
be rotated relative to the biological tissue, thus offering additional areas of access to the tissue.
Support block assemblies 26 and 27 rigidly fasten Y-axis track 28 to anchor block 25, and thus tissue support table 14. Y-axis linear encoder 29 comprises, for example, an incremental binary counter, and is slidably movable along the length of
Y-axis track 28. In a preferred embodiment, the Y-axis track has disposed within it a printed circuit board arrangement of parallel, spaced-apart copper strips, while Y-axis linear encoder 29 includes a head that senses the static capacitance of the
copper strips as the encoder is manually slid along Y-axis track 28, and circuitry for interpolating between adjacent copper strips. As Y-axis linear encoder 29 is moved along track 28, it outputs a signal corresponding to its displacement from a preset
reference point, preferably, a hard stop at a distal-most position from the patient's chest wall. The signal output by linear encoder 29 is provided to computer 20 via connecting cable 21, which connects to encoder 29 through jack 21a.
Support plate assembly 30 rigidly connects Z-axis linear encoder 32 to Y-axis linear encoder 29. Z-axis track 31 is slidably engaged in linear encoder 32, so that linear encoder 32 generates a signal corresponding to the displacement of Z-axis
track relative to linear encoder 32 when track 32 is raised and lowered. The signal output by linear encoder 32 is provided to computer 20 via connecting cable 21, which connects to encoder 32 through jack 21b. Linear encoder 32 may use, for example,
either the upper surface of tissue support table 14, or the lower surface of ultrasonic scanner 13, as its reference point. Linear encoders 29 and 32 preferably have a displacement accuracy of about plus/minus 0.05 mm, and can be reset via switches on
encoders 29 and 32, or via software control.
Linear encoder 29 includes means, not shown, for locking the encoder in position along Y-axis track 28, while linear encoder 32 includes means (not shown) for locking Z-axis track 31 in position in encoder 32. Linear encoders 29 and 32, and
mating tracks 28 and 31, are available from Sylvac S. A., Crissier, Switzerland, and distributed in the United States by Fowler Company, Inc., Chicago, Ill., as Part Nos. 54-050-035 (for Y-axis encoder 29) and 54-050-000 (for Z-axis encoder 32).
In addition, as will of course be understood by persons of skill in the art, linear encoders 29 and 32 may also comprise suitably designed rotary encoders, for example, as are used in computer mice and videogame joysticks, or other suitable
displacement sensing components, such as linear variable displacement transducers or linear potentiometers.
Needle support assembly 33 comprises a biopsy needle holder that holds the biopsy needle securely during initial positioning and insertion, but detachably releases biopsy needle to allow free-hand movement of the biopsy needle once it has been
inserted into a patient's tissue.
In the illustrative embodiment of FIG. 2, needle support assembly includes upper block 33a and lower block 33b. Needle support member is detachably coupled to the upper end of Z-axis track 31, for example, by a slot (not shown) in the lower
surface of lower block 33b. Upper block 33a includes semi-circular channel 33c in its lower surface while lower block 33b includes semi-circular channel 33c in its upper surface. The channels in upper block 33a and lower block 33b mate when the two
pieces are positioned together, thus forming a bore through which biopsy needle 19 may be slidably disposed.
Upper block 33a and lower block 33b preferably also have mating projections and concavities, for example, in the illustrative embodiment of FIG. 2, block-like projection 33e and corresponding indentation 33f. Bore 33g aligns across upper block
33a and lower block 33b when the two blocks are mated together, to permit pin 33d to be slidably disposed in bore 33g. In this manner, upper block 33a and lower block 33b may be rigidly fastened together by pin 33d to carry biopsy needle 19 during
initial positioning and insertion of biopsy needle 19. When inserted in the bore formed by channels 33c, the biopsy needle has a trajectory aligned with the bore.
Once the needle is inserted in the patient, pin 33d may be removed from bore 33g, permitting removal of upper block 33a and movement of lower block 33b out of the clinician's way. This arrangement permits the clinician to thus remove the biopsy
needle from needle support assembly 33 and manipulate it manually, while observing movement of the needle tip via display 23. Accordingly, needle support assembly 33 permits the biopsy needle to be initially positioned with the accuracy of a
stereotactic biopsy system, while providing the flexibility and maneuverability of free-hand ultrasound techniques.
An alternative illustrative embodiment of needle support assembly 33' is described with respect to FIGS. 3A-3B. As shown in FIG. 3A, needle support assembly 33' co | | |