Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
CA 0223~702 1998-0~-13
WO97/18751 PCT~S96/18592
1 STEREOTACTIC BREAST BIOPSY COIL
2 AND METHOD FOR USE
3 BACKGROUND OF THE INVENTION
4 The present invention relates to MRI-guided tissue biopsy
and, in particular, to a stereotaxic breast biopsy coil.
6 Magnetic resonance imaging (MRI) can detect breast
7 malignancies that have previously been sub-clinical (i.e.,
8 neither palpable nor detected by mammography). Unfortunately,
9 a 40 percent false positive rate goes along with this detection.
This results in a large number of extremely invasive open
11 biopsies being performed.
12 It iS desirable to use less invasive methods such as a
13 needle biopsy (core or aspiration), but needle placement re~uires
14 1 mm accuracy in three dimensions.
SUMMARY OF THE INVENTION
16 An MRI coil for providing an image of a protuberance of
17 tissue has a tubular wall having a longitudinal proximal portion
18 adapted to receive the protuberance and a longitudinal distal
19 portion. The wall includes a transverse access portal between
the distal and proximal portions. This portal eliminates a
21 substantial portion of the wall. A first coil portion is located
22 about the distal portion and a second coil portion is located
23 about the proximal portion.
24 BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a perspective view of a coil according to the
26 invention from above with a portion exploded.
27 FIG. 2 is a front perspective view of a coil according to
28 t~e invention.
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1 FI&. 3 is a top plan view of the a coil according to the
2 invention.
3 FIG. 4 is front elevation view of a needle guide according
4 to the invention.
FIG. 5 is a graphical view of the geometry of an embodiment
6 of the invention.
7 DESCRIPTION OF THE PREFERRED EMBODIMENTS
8 Referring to FIGS. 1, 2 and 3, a breast biopsy coil lO
9 includes a base 12 to which is attached a tubular wall 14 and
three fiducials 16, 18, 20.
11 A ring 22 abuts the external junction of the base 12 and the
12 wall 14. The ring 22 is rotatable about its axis and is slidably
13 retained between the fiducials 16, 18, 20 and base 12 and wall
14 14. A needle guide 24 is removably attached to the ring 22.
These structures can be formed from a suitable non-magnetic, MRI
16 transparent material such as a thermoplastic pol~7mer of methyl
17 methacrylate (e.g., Plexiglas).
18 The wall 14 includes a large aperture or portal 26. The
19 wall 14 contains a slot 28 for receiving a sheath 30. The sheath
30 may be, for example, a thin sheet of plastic of moderate
21 stiffness and being relatively easy to puncture with a sharp
22 instrument (e.g., 15 mil thick polyurethane film such as TEXIN
23 brand polyurethane film from Bayer Polymers Division, Bayer
24 Corporation, or 1/32 inch thick Huntsman ~igh Impact Polystyrene
- Medical Grade).
26 The interior of the wall opposite the portal 26 is provided
27 with an inflatable bladder 32. The bladder 32 may be, for
28 example, formed of latex rubber.
29 The coil 10 may have, for example, an internal diameter of
17.8 cm an~ a height of 7 cm. This provides an internal volume
31 of about 1740 ml for ease of breast placement. When the bladder
32 32 is fully inflated, this volume may be, for example, reduced
33 to 9OO ml.
. .
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1 The proximal portion of the wall 14 contains a portion 34
2 of an electrical coil about its circumference. Similarly, the
3 distal portion of the wall 14 contains a portion 36 of an
4 electrical coil about its circumference. The electrical coil
portions 34, 36 may be, for example, single turns. The
6 electrical coil portions are connected by an unshown matching
7 network to a cable 38 and include capacitive splits, a detuning
8 diode, and current traps to protect the coil during transmission
9 by an unshown imager. such features are set forth in U.S. Patent
Application Serial Number 08/530,576, filed September 19, 1995,
11 and incorporated herein by reference. The coil may operate, for
12 example, at 63.89 MHz. The distal and proximal coil portions
13 allow for the portal to be, for example, 5.7 cm high and to
14 extend around nearly 180 degrees of the wall 14.
The base 12 can be provided with a graduated scale 38 to
16 provide an azimuthal positioning of the needle guide 24 as the
17 ring 22 is rotated.
18 Referring to FIG. 4, the needle guide 24 has a series of
19 guide bores 40. The bores 40 are in two staggered rows to
provide increased spatial resolution. For use with an 18 gauge
21 needle (nominally 1 mm), the bores 40 are bored 0.07 mm over
22 needle size. They are on 2 mm centers with the staggering
23 providing plus or minus 0.5 mm resolution in the vertical
24 direction. A different guide 24 is provided for each size needle
to be used. The guide 24 can be conveniently made to insert into
26 a receptacle in the ring 22. The number of staggered rows can
27 be varied to insure the desired resolution for different
28 needle/bore sizes.
29 In general, a needle 42 inserted into the guide 24 will
follow a radial path with respect to the ring 22. The
31 graduations scale 38 may be, for example, spaced to provide 1.5
32 mm arc len~th at the interior of the wall 14. This then provides
33 a resolution of plus or minus 0.77 mm at the wall 14 and as the
34 needle tip continues to the center the resolution approaches
zero.
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WO97/187S1 PCT~S96/18592
1 The depth of insertion of the needle 42 can be conveniently
2 determined, for example, by either a graduated scale on the
3 needle or a moveable stop placed on the needle to prevent further
4 insertion through a guide bore 40.
The combination of adjusting the ring 22 in azimuth,
6 choosing the proper guide bore 40 and inserting the needle 42 a
7 desired depth into the guide bore can easily provide better than
8 1 mm resolution for positioning the needle tip in three
9 dimensions within the coil lO.
The vertical fiducials 16, 18 consist of 5 mm bores parallel
11 to the axis the coil lO. The fiducials 16, 18 are located on a
12 diameter of the ring 22. The fiducial 20 consists o~ a 5 mm bore
13 at an angle to the fiducial 18. The bores of the fiducials 18,
14 20 intersect to ~orm the zero height reference of the coil lO.
The angle between the fiducials 18, 20 may be, for example, 45
16 degrees. The bores are filled with a material that will provide
17 an MRI image, for example, 0.04M CuSo4-5H2O.
18 In operation, a breast or other protuberance of tissue is
19 inserted into the proximal portion 34 of the wall 14 and extends
toward the distal portion 36. In the preferred embodiment, the
21 patient lies in a prone position upon the coil lO (with suitable
22 surrounding support3.
23 The bladder 32 is inflated by unshown means to compress the
24 breast against the portal 26. The sheath 30 keeps the breast
from "leaking" in a transverse direction out of the portal 26.
26 The sheath 30 provides support of the lateral portion of breast.
27 Despite the large portal 24, there is no compromise of
28 immobilization. The sheath 30 is readily replaceable between
29 patients or procedures.
The breast is then imaged using the coil lO with an unshown
31 MRI imager. Referring to FIG. 5, in a coronal image, the
32 fiducials ~8, 20 produce dots separated by a distance d. The
33 height h above the base of the coil is given by: h = d-tan(45~).
34 I~ the coordinates of the fiducials 16, 18 are ~x1~ Y1) and
tXz~ Y2), respectively, then the midpoint between them (xm/ Ym) is
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A l given by: (xm, Ym) = ((x1 + x2)/2, (Y1 ~ y2)/2). The distance
2 between the fiducials 16, 18 is D given by: D = (~x1 - x2)Z + (Y
3 - y2)2)(1/Z)
4 The distance p from the midpoint to the imaged lesion or
target (Xt, Yt) is given by: p = ((xt - Xm) 2 + (Yt - y~) 2~ ~1/2), The
6 distance c from the fiducial 16 to the target is given by c =
7 ((xt ~ x2)2 ~ (Yt + Y2)Z)(1/2) The azimuthal angle ~ is given by:
8 ~ = arCcos((c2 _ p2 -(~/2)2)/( 2.p.(D/2))
9 The needle insertion length N i5 given by: N = R - p where
R is the length of the needle. Thus the image can be used to
ll provide the anteroposterior distance, the needle insertion
12 length, and the angular position necessary to locate the target
13 in three dimensions and insert the tip the needle 42 to that
14 location.
Based on the data from the image, the needle guide 24 is
l~ rotated to the correct azimuth and the needle inserted into the
17 correct guide bore 40. The needle 42 is then inserted through
18 the sheath 30 into the breast (the needle and sheath are sterile)
l9 to the desired depth. For particularly large bore needles, the
breast skin (and the sheath) can be nicked to assist in inserting
2l the needle. The tip of the needle is then located within less
22 than l mm of the desired location.
23 A biopsy of the lesion can be performed by using either a
24 coring biopsy needle or an aspiration biopsy needle. In
addition, because of MRI detects tumor borders more accurately
26 than other modalities, the needle can be used to localize the
27 lesion.
28 The large po!rtal 24 provides ready access to any point
29 within the breast and makes such procedures as skin nicks easy
to accomplish. This large portal 24 is made possible by the
3l sheath 30.
32 The s~eath 30 provides support and immobilization for the
33 tissue, while still permitting access to any location of the
34 tissue with needles or other puncturing or cutting instruments.
This combination of portal and sheath can be used in other
CA 0223~702 1998-0~-13
WO97/18751 PCT~S96/18592
l coil/frame structures, for example, a tubular wall having an oval
2 or rectangular cross-section, or a frustoconical chamber can be
3 conveniently provided with a large portal that can be covered
4 with a sheath.
In the preferred embodiment, the necessary position settings
6 for the needle 42 are automatically calculated by either software
7 in the imager or in an auxiliary computer such as a laptop
8 computer.
9 The coil lO as described provides needle access to within
about l cm of the chest wall. If access to the blocked area is
ll desired, the needle guide 24 can be provided with guide bores at
12 a polar angle to the plane o~ the coil. With minor modifications
13 to the calculations, the needle can then be accurately inserted
14 into this area.
Other configurations of the invention are also possible, for
16 example, the electrical coil portions 34, 36 can be provided in
17 the form of a separate electrical coil or coils that are placed
18 about the coil lO during operation. The coil lO is then more
l9 accurately described as a frame even though its structure remains
otherwise unchanged. This structure provides a stereotactic
21 frame for orienting a needle. It also may be advantageous to use
22 the coil lO in combination with additional electrical coil
23 geometries (e.g.,. Helmoltz, saddle, or surface coil), either
24 integral or external.
It should be evident that this disclosure is by way of
26 example and that various changes may be made by adding, modifying
27 or eliminating details without departing from the fair scope of
28 the teaching contained in this disclosure. The invention is
29 therefore not limited to particular details of this disclosure
except to the extent that the following claims are necessarily
3l so limited.
.
