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AJR 2000; 174:753-756
© American Roentgen Ray Society


Original Report

Mammographic Abnormalities Caused by Percutaneous Stereotactic Biopsy of Histologically Benign Lesions Evident on Follow-Up Mammograms

Robert L. Lamm1 and Roger J. Jackman

1 Both authors: Department of Radiology, Palo Alto Medical Clinic, 795 El Camino Real, Palo Alto, CA 94301

Received October 19, 1998; accepted after revision August 9, 1999.

 
Supported in part by an educational grant from Biopsys Medical, Inc., to the Palo Alto Medical Foundation.

R. J. Jackman was formerly a shareholder in and a clinical consultant to Biopsys Medical, Inc.

Address correspondence to R. L. Lamm.


Abstract
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The purpose of our study was to evaluate how often a mammographic abnormality thought to be produced by the biopsy procedure was evident on the initial follow-up mammogram after percutaneous biopsy of impalpable histologically benign lesions. We compared three stereotactic percutaneous biopsy methods.

CONCLUSION. A mammographic density seen well only in the projection parallel to the biopsy needle tract was evident in 2% (5/226) of the lesions for which 11-gauge directional vacuum-assisted biopsy was used, 0% (0/96) of the lesions for which 14-gauge directional vacuum-assisted biopsy was used, and 0% (0/422) of the lesions for which 14-gauge automated large-core biopsy was used. No mammographic abnormalities assessed as BI-RADS categories 3, 4, or 5 (according to the American College of Radiology's Breast Imaging Reporting and Data System) and thought to be produced by the biopsy procedure were evident after any of the biopsy methods.


Introduction
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Percutaneous stereotactic breast biopsy is rapidly gaining acceptance as the procedure of choice in obtaining a histopathologic diagnosis for impalpable mammographic lesions requiring biopsy. Methodologic options include 14-gauge automated large-core biopsy and directional vacuum-assisted biopsy (Mammotome; Biopsys Medical [Ethicon Endo-Surgery], Cincinnati, OH) with 14- and 11-gauge probes. In prior studies, investigators have found no suspicious changes or distortion thought to be caused by the biopsy procedure on the first mammogram after biopsy of histologically benign lesions with either of the 14-gauge devices [1,2,3] or the 11-gauge probe [3].

We describe a postbiopsy mammographic density seen well only in the mammographic projection parallel to the biopsy needle tract on the initial mammogram obtained 6-8 months after stereotactic biopsy of histologically benign lesions. The density was evident only after 11-gauge directional vacuum-assisted biopsies. We suggest the density is caused by minor postbiopsy scar tissue that is most prominent when viewed along the z-axis of the biopsy probe.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
From July 1991 through December 1997 we performed 1367 percutaneous stereotactic breast biopsies on impalpable mammographically detected lesions using a prone table (Mammotest; Fischer Imaging, Denver, CO). Percutaneous histologic results were benign in 824 lesions. Twenty-nine of these lesions were biopsied a second time (27 surgical biopsies and two percutaneous biopsies) before mammographic follow-up and were excluded from the study. Of the remaining 795 lesions, mammographic follow-up was performed in 744 lesions, which constitute our study group. Of these 744 lesions, 422 were biopsied from July 1991 to mid-April 1995 using 14-gauge automated large-core technique; 96 from mid-March 1995 to mid-June 1996 using 14-gauge directional vacuum-assisted technique; and 226 from mid-May 1996 through December 1997 using 11-gauge directional vacuum-assisted technique. The mean number of specimens for each technique was nine, 18, and 18, respectively. During the 1-month overlaps between biopsy techniques, the availability of the newer biopsy probe determined which technique was used. Mammographic follow-up of the histologically benign lesions was advised to occur at 6 or 12 months after biopsy and was actually performed at 1-53 months (median, 7 months). Of these 744 follow-up mammograms, 22 were performed 1-4 months after biopsy, 700 were performed 5-18 months after biopsy, and 22 were performed 19-53 months after biopsy.

A retrospective review of the first postbiopsy mammograms for these 744 lesions with benign histology was performed to assess the presence or absence of postbiopsy mammographic changes. All first postbiopsy mammograms consisted of craniocaudal and mediolateral oblique views with additional views obtained only if requested by the radiologist initially interpreting the follow-up examination.


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
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In none of the cases did the first follow-up mammogram after benign percutaneous breast biopsy reveal a postbiopsy abnormality assessed as category 3, 4, or 5 (in the American College of Radiology's Breast Imaging Reporting and Data System [BI-RADS]) [4] thought to be caused by the biopsy procedure. In 2% (5/226) of the lesions biopsied with 11-gauge directional vacuum-assisted technique, the first follow-up mammogram revealed a density (BI-RADS category 2) with similar features in each case. None of these densities was evident on follow-up mammograms after 14-gauge automated large-core biopsy or 14-gauge directional vacuum-assisted biopsy.

Lesion, biopsy, and follow-up variables of the five lesions with postbiopsy densities are shown in Table 1. These five biopsied lesions consisted of two masses and three clusters of microcalcifications; all were assessed as BI-RADS category 4 (suspicious) lesions. No complications were present during or immediately after the biopsy in any of the five cases. The five biopsied lesions had removal of 12-26 specimens (mean, 19 specimens) as compared with removal of 4-70 specimens (mean, 18 specimens) for the entire cohort of 11-gauge directional vacuum-assisted biopsied lesions in the study group.


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TABLE 1 Lesion Type on II-Gauge Directional Vacuum-Assisted Biopsy and Variables on Follow-Up Mammography for Five Lesions

 

Histopathologic study revealed nonspecific benign findings in all five lesions. Nonproliferative fibrocystic changes were found in both masses and one of the microcalcification lesions. The other two microcalcification lesions revealed fat necrosis, inflammation, and fibrosis and proliferative and fibroadenomatous changes, respectively. Specimen radiographs revealed calcium in all three microcalcification lesions.

Immediate postbiopsy stereotactic digital images were obtained in four of these five patients and showed that the lesion in question was gone; no postbiopsy hematomas were evident. In these same four patients, a stainless-steel clip (Micromark; Biopsys Medical) was deployed to mark the biopsy site. Each clip was less than 10 mm from the biopsy cavity margin. At the time of the first follow-up mammogram, obtained 6-8 months after biopsy, the biopsied lesion was gone and a new mammographic density was present in all five patients. The densities were small (maximum diameter, 5-10 mm; mean diameter, 8 mm), dense, and round or oval with irregular or spiculated margins in the craniocaudal projection only. In all five patients, a craniocaudal needle biopsy approach was used (i.e., the density was well seen only along the z-axis of the biopsy probe). In the mediolateral oblique projection, the densities were imperceptible in two patients (Fig. 1A,1B,1C,1D) and were extremely faint in three patients with a maximum diameter of 23-30 mm (mean, 27 mm).



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Fig. 1A. —73-year-old woman with history of benign percutaneous right breast biopsy using 11-gauge directional vacuum-assisted technique. Craniocaudal (A) and mediolateral oblique (B) prebiopsy right mammograms show 8-mm cluster of pleomorphic microcalcifications in upper outer quadrant. Calcification anterior to clustered biopsied calcifications on B is located 8 cm medially.

 


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Fig. 1B. —73-year-old woman with history of benign percutaneous right breast biopsy using 11-gauge directional vacuum-assisted technique. Craniocaudal (A) and mediolateral oblique (B) prebiopsy right mammograms show 8-mm cluster of pleomorphic microcalcifications in upper outer quadrant. Calcification anterior to clustered biopsied calcifications on B is located 8 cm medially.

 


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Fig. 1C. —73-year-old woman with history of benign percutaneous right breast biopsy using 11-gauge directional vacuum-assisted technique. Craniocaudal (C) and mediolateral oblique (D) right mammograms obtained 6 months after percutaneous biopsy show 7-mm spiculated density on C and no perceptible density on D. Metallic clip marks biopsy site. Slight increase in density of background scattered fibroglandular tissue is presumed related to hormone replacement therapy that was started 6 months before these mammograms were obtained. Calcification inferior to metallic clip on D is situated 8 cm medial to biopsied calcifications. Punctate opacity anterior to metallic clip on D represents artifact.

 


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Fig. 1D. —73-year-old woman with history of benign percutaneous right breast biopsy using 11-gauge directional vacuum-assisted technique. Craniocaudal (C) and mediolateral oblique (D) right mammograms obtained 6 months after percutaneous biopsy show 7-mm spiculated density on C and no perceptible density on D. Metallic clip marks biopsy site. Slight increase in density of background scattered fibroglandular tissue is presumed related to hormone replacement therapy that was started 6 months before these mammograms were obtained. Calcification inferior to metallic clip on D is situated 8 cm medial to biopsied calcifications. Punctate opacity anterior to metallic clip on D represents artifact.

 


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
The mammographic changes after surgical excisional breast biopsy for both benign and malignant lesions have been well described and include skin thickening and distortion, architectural distortion, parenchymal scar (poorly defined mass, often with spiculated margins, detected on right-angle projections), calcifications, opaque foreign body, fat necrosis, and asymmetric glandular tissue defect [5,6,7,8,9,10]. Of these findings, the skin changes and architectural distortion may mimic indirect mammographic signs of malignancy, and the parenchymal scar and calcifications may mimic direct mammographic signs of malignancy. When detected in two projections, these postsurgical mammographic changes alone or in combination produce a mammographic lesion suggestive of carcinoma (Fig. 2A,2B). These lesions have been found to show regression or stability over time on follow-up mammographic examinations [6,7,8,9,10]. This allows the mammographer who is cognizant of the history and location of prior surgical biopsy to follow such stable or regressing mammographic lesions without further intervention.



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Fig. 2A. —75-year-old woman with history of needle-localized lumpectomy and radiation therapy for right breast impalpable infiltrating ductal carcinoma. Craniocaudal (A) and mediolateral oblique (B) right mammograms show 12-mm spiculated mass in upper outer quadrant at lumpectomy site. Lesion has been stable for 7 years after lumpectomy.

 


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Fig. 2B. —75-year-old woman with history of needle-localized lumpectomy and radiation therapy for right breast impalpable infiltrating ductal carcinoma. Craniocaudal (A) and mediolateral oblique (B) right mammograms show 12-mm spiculated mass in upper outer quadrant at lumpectomy site. Lesion has been stable for 7 years after lumpectomy.

 

In patients who have undergone uncomplicated percutaneous stereotactic automated large-core or directional vacuum-assisted biopsy for benign disease, no mammographic lesions thought to be caused by the biopsy procedure have been detected on follow-up mammograms [1,2,3]. Our experience with the first follow-up mammograms for benign lesions biopsied with the 14-gauge automated large-core technique and with the 14-gauge directional vacuum-assisted technique has been similar to those of other literature reports with no postbiopsy mammographic changes detected. In 2% (5/226) of the benign lesions biopsied using the 11-gauge directional vacuum-assisted technique, a postbiopsy mammographic density was observed.

Unlike the mammographic lesion after surgical excision, which is typically well seen in two projections, the lesion after 11-gauge biopsy is only well seen in one projection and is either faintly detectable or imperceptible in the oblique or orthogonal projections. Because this lesion is seen as a conspicuous finding in only one projection, it is best described as a density in accordance with BI-RADS terminology [4]. Knowing that the density is at the site of a prior 11-gauge biopsy allows one to categorize it as a BI-RADS category 2 (benign) lesion; proximity of a postbiopsy metal clip to the density increases confidence in the benign categorization.

The mammographic features of this lesion are likely directly related to the biopsy technique. Specifically, with the 11-gauge directional vacuum-assisted biopsy, an approximately cylindric tissue sample, much longer than it is wide, is removed. In every one of the lesions we observed, the density appeared small and most dense in the projection parallel to the biopsy needle tract and appeared vague or imperceptible in the oblique or orthogonal projection. In other words, the lesion is thought to be a minor postbiopsy scar that appears most conspicuous when viewed along the z-axis of the biopsy probe.

Presumably a scar would be more apt to occur after biopsies in which more tissue was removed. Although we obtained an average of 18 specimens per lesion during directional vacuum-assisted biopsy with both 14-gauge probes and the 11-gauge probe, we did not find any lesions after 14-gauge biopsy. This difference is likely explained by the greater average weight of an individual specimen obtained with an 11-gauge probe (95 mg) than that obtained with a 14-gauge probe (37 mg) [11,12,13].

We would expect an occasional lesion to occur after 14-gauge directional vacuum-assisted biopsy, especially if a large number of specimens were removed.

It is important that the mammographer interpreting follow-up mammograms after biopsy of benign lesions with 11-gauge directional vacuum-assisted technique is aware of the features of this lesion and its relation to the biopsy procedure. We now specify the direction of the biopsy approach in our dictated reports of all percutaneous breast biopsies to facilitate evaluation of these lesions on follow-up mammograms. The recognition of this characteristic finding should obviate further mammographic workup and should prevent misinterpretation as a lesion requiring further intervention. Additional studies are needed to evaluate the incidence of this finding in larger series. In all five of our patients, a second follow-up mammogram was obtained at 12-21 months (mean, 14 months), and in one patient, a third follow-up mammogram was obtained at 25 months. In every patient, the postbiopsy lesion was either unchanged or showed a definite decrease in density. These results suggest that these postbiopsy lesions either remain stable or regress with time in the same manner as the lesions seen after surgical biopsy.


Acknowledgments
 
We thank Julie C. Clark for her diligence and perseverance in the preparation of this manuscript.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Kaye MD, Vicinanza-Adami CA, Sullivan ML. Mammographic findings after stereotaxic biopsy of the breast performed with large-core needles. Radiology 1994;192:149-151[Abstract/Free Full Text]
  2. Burbank F. Mammographic findings after 14-gauge automated needle and 14-gauge directional, vacuum-assisted stereotactic breast biopsies. Radiology 1997;204:153-156[Abstract/Free Full Text]
  3. Jackman RJ, Marzoni FA, Nowels KW. Percutaneous removal of benign mammographic lesions: comparison of automated large-core and directional vacuum-assisted stereotactic biopsy techniques. AJR 1998;171:1325-1330[Abstract/Free Full Text]
  4. American College of Radiology. Breast imaging reporting and data system (BI-RADS), 3rd ed. Reston, VA: American College of Radiology, 1998
  5. Sickles EA, Herzog KA. Intramammary scar tissue: a mimic of the mammographic appearance of carcinoma. AJR 1980;135:349-352[Abstract]
  6. Sickles EA, Herzog KA. Mammography of the post-surgical breast. AJR 1981;136:585-588[Abstract/Free Full Text]
  7. Homer MJ. Mammographic appearance of the breast after needle localization and biopsy. Breast 1985;2:26-31
  8. Dershaw DD, Shank B, Reisinger S. Mammographic findings after breast cancer treatment with local excision and definitive irradiation. Radiology 1987;164:455-461[Abstract/Free Full Text]
  9. Brenner RJ, Pfaff JM. Mammographic features after conservation therapy for malignant breast disease: serial findings standardized by regression analysis. AJR 1996;167:171-178[Abstract/Free Full Text]
  10. Brenner RJ, Pfaff JM. Mammographic changes after excisional breast biopsy for benign disease. AJR 1996;167:1047-1052[Abstract/Free Full Text]
  11. Burbank F, Parker SH, Fogarty TJ. Stereotactic breast biopsy: improved tissue harvesting with the Mammotome. Am Surg 1996;62:738-744[Medline]
  12. Burbank F. Stereotactic breast biopsy: comparison of 14- and 11-gauge Mammotome probe performance and complication rates. Am Surg 1997;63:988-995[Medline]
  13. Berg WA, Krebs TL, Campassi C, Magder LS, Sun CCJ. Evaluation of 14- and 11-gauge directional, vacuum-assisted biopsy probes and 14-gauge biopsy guns in a breast parenchymal model. Radiology 1997;205:203-208[Abstract/Free Full Text]

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