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DOI:10.2214/AJR.07.2658
AJR 2008; 191:1216-1219
© American Roentgen Ray Society


Original Research

Sonographically Guided Marker Placement for Confirmation of Removal of Mammographically Occult Lesions After Localization

Cecilia L. Mercado1, Amber A. Guth2, Hildegard K. Toth1, Linda Moy1, Deborah Axelrod2 and Joan Cangiarella3

1 Department of Radiology, New York University School of Medicine, New York University Cancer Institute, 160 E 34th St., 3rd Fl., New York, NY 10016.
2 Department of Surgery, New York University School of Medicine, New York, NY.
3 Department of Pathology, New York University School of Medicine, New York, NY.

Received June 1, 2007; accepted after revision September 9, 2007.

 
Address correspondence to C. L. Mercado (cecilia.mercado{at}med.nyu.edu).


Abstract
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. We evaluated the benefit of placing a marker under sonographic guidance at the time of localization to aid in identifying mammographically occult lesions within the specimen at the time of surgical excision and to evaluate margin status.

MATERIALS AND METHODS. We reviewed 135 sonographically guided needle localizations performed on mammographically occult lesions. Imaging during the localization procedure, marker placement, and specimen radiographs were reviewed, and the findings were correlated with the histopathologic findings.

RESULTS. Of the 135 mammographically occult lesions, 77 were localized without marker placement and 58 with marker placement. The 58 localizations with marker placement were for masses with a mean lesion size of 9 mm. Specimen radiography of these lesions showed a marker within the specimen in 56 cases (97%) and visualization of the lesion in only seven cases (12%). Specimen radiography of localizations without marker placement showed visualization of the lesion in 18 cases (23%). Of the 11 malignant lesions (19%) localized with marker placement, none had a positive inked margin, but five (46%) had close margins necessitating reexcision. Of the 26 malignant lesions (34%) localized without marker placement, two (8%) had a positive inked margin, and eight (31%) had close margins necessitating reexcision.

CONCLUSION. At needle localization of breast lesions, marker placement under sonographic guidance is beneficial because it enables immediate confirmation of accurate surgical removal of the localized lesion at surgical excision. Use of marker placement, however, does not reduce the percentage of cases with close margins necessitating reexcision.

Keywords: breast • breast specimen • mammography • sonography


Introduction
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Sonography is commonly used for characterization of breast masses, for guidance of diagnostic procedures such as aspiration and core biopsies, and for preoperative needle localization [1, 2]. Procedures performed with sonographic guidance are more advantageous owing to lack of ionizing radiation and breast compression, increasing safety, patient comfort, and ease and speed of performance [3, 4]. Sonography is especially useful for needle localization of lesions not visualized with mammography. Specimen radiography or specimen sonography can be used to confirm surgical removal of lesions that have been localized with sonographic guidance [5, 6]. In instances in which specimen sonography is not feasible, confirmation of surgical removal is solely dependent on specimen radiography. If the lesion is not visible with mammography, assurance of surgical removal can be difficult.

The introduction of sonographically placed breast markers facilitates radiographic identification of the location of mammographically occult lesions. Breast markers are commonly used after breast biopsy when complete obliteration of a lesion is suspected owing to small lesion size or before neoadjuvant chemotherapy for verification of the site of breast cancer after treatment [7, 8]. However, breast markers are not always placed after all sonographically guided diagnostic procedures. We sought to evaluate the benefit of placing a breast marker under sonographic guidance at needle localization to aid in identifying mammographically occult lesions within the specimen at surgical excision and to evaluate margin status.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Study Group
Six hundred twenty-eight consecutive needle localizations during the 21-month period September 1, 2004, to June 30, 2006, were retrospectively reviewed. Needle localizations were performed by one of six radiologists specializing in breast imaging, and surgical excisions were performed by one of six breast surgeons. Of the 628 needle localizations, 301 (48%) were performed under sonographic guidance, and 157 of those (25% of the 628) revealed mammographically occult lesions. Twenty-one of the 157 procedures were excluded because of the presence of a marker at the biopsy site placed during previous percutaneous biopsy, and one was excluded because of lack of availability of specimen radiography. The other 135 procedures (21% of the original 628) constitute the basis of this study. This retrospective study was approved by the institutional review board. The 135 procedures were performed on 123 women (mean age, 48 years; range, 25–86 years). In all cases, the lesions localized were sonographically visualized. The procedures were divided into two groups: those in which a marker was placed during the needle localization procedure and those in which a marker was not placed.

Imaging
The mammographic and sonographic images obtained during the needle localization and marker placement procedures were retrospectively reviewed for evaluation of lesion type, lesion size, and appropriate wire and marker placement. The distance between the localizing wire and the marker was ascertained from postprocedure mammograms. In all cases, specimen radiographs were retrospectively reviewed for visualization of the targeted lesion and for wire and localizing markers if placed.


Figure 1
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Fig. 1A 46-year-old woman without symptoms. Sonogram of left breast shows oval hypoechoic solid mass with circumscribed margins and without posterior acoustic enhancement or shadowing. Cytologic examination of specimen from sonographically guided fine-needle aspiration revealed atypical cells.

 


Figure 2
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Fig. 1B 46-year-old woman without symptoms. Sonogram of left breast obtained during needle localization procedure shows localization wire (arrows) coursing through lesion.

 


Figure 3
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Fig. 1C 46-year-old woman without symptoms. Sonogram of left breast obtained during placement of localizing marker shows collagen plug with embedded marker (arrow) visible as linear structure of increased echogenicity within lesion.

 


Figure 4
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Fig. 1D 46-year-old woman without symptoms. Left mediolateral oblique mammogram obtained after sonographically guided needle localization and marker placement procedures shows localizing marker (arrow) adjacent to localizing wire. Mass is mammographically occult and not visible. Retroglandular saline implant is evident.

 


Figure 5
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Fig. 1E 46-year-old woman without symptoms. Specimen radiograph shows localizing marker (arrow) within specimen adjacent to localizing wire. Localized lesion is not well depicted. Marker is used to confirm surgical removal of lesion. Histopathologic finding was tubular adenoma.

 
Needle Localization and Clip Placement Procedures
Sonographically guided preoperative needle localization was performed with a 21-gauge modified Kopans spring-hook localization needle inserted into and through the lesion under sono graphic guidance with a freehand technique. The hookwire was then inserted through the needle, and the needle was removed. In cases in which a breast marker was placed after needle localization, a 14-gauge introducer and sonographic guidance were used to place a localizing clip embedded in a bioresorbable col lagen plug (Cormark, Ethicon Endo-Surgery) into or adjacent to the lesion. Marker placement was per formed on some lesions according to surgeon preference. Postprocedure craniocaudal and 90° mediolateral mammograms were obtained to ensure proper placement of the wire and marker (Fig. 1A, 1B, 1C, 1D, 1E). Radiographs (Faxitron unit, Faxitron X-Ray Corporation) of the surgical specimen were obtained to confirm surgical removal of the lesion or marker at the surgical procedure.

Pathologic Evaluation
The histopathologic findings on the surgical specimens were reviewed by a pathologist with expertise in breast pathology and were correlated with the imaging findings. In all malignant cases, the proximity to the inked margins was assessed microscopically for evaluation of the surgical margins. The specimens were grouped into three categories depending on whether the margins were positive (lesion at inked margin), close (1–4 mm from the margin), or negative (5 mm or more from the margin).

Statistical Analysis
The cases with and without marker placement were compared with respect to each proportion shown in Table 1. The Mann-Whitney test was used for patient age and lesion size, and Fisher's exact test was used for specimen radiography, histologic finding, and margins. Each reported p value was two-sided and not subjected to multiple comparison correction.


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TABLE 1: Findings at Specimen Radiography and Histopathology for Needle Localizations With and Without Marker Placement

 


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Study Population and Lesions
The 58 localizations with marker placement were performed on 56 women (mean age, 47 years; range, 29–73 years). The mean lesion size was 9 mm (range, 2–21 mm). The 77 localizations without marker placement were performed on 67 women (mean age, 49 years; range, 25–86 years). The mean lesion size was 10.5 mm (range, 3–40 mm). The mean patient age and mean lesion size for both groups of needle localizations with and without marker placement were similar (Table 1). Eighty of the 135 lesions (59%) had been subjected to sonographically guided fine-needle aspiration or core needle biopsy before surgical removal. In the 77 needle localizations without marker placement, 28 lesions had been subjected to sonographically guided fine-needle aspiration and 16 lesions, to sonographically guided core needle biopsy. Among the 58 needle localizations with marker placement, 24 lesions had been subjected to sonographically guided fine-needle aspiration and 12 lesions, to sonographically guided core needle biopsy.

In all cases postprocedure mammograms showed appropriate marker deployment in the specific quadrant of the breast near the localizing wire. Because the exact distance between the mammographically occult lesions and the markers could not be ascertained on the postprocedure mammograms, the distances between the localizing wires and the markers were measured; the mean distance was 0.3 cm (range, 0–1.1 cm). There were no complications of the marker placement procedure.

Specimen Radiography
Specimen radiography of needle localizations with marker placement showed a marker within the specimen in 56 cases (97%) and visualization of the lesion in only seven cases (12%). In the two cases (3%) in which a marker was not identified in the specimen, follow-up mammography did not depict the marker within the breast, confirming marker removal during the surgical procedure. Conversely, specimen radiography of localizations without marker placement depicted the lesion in 18 cases (23%). The percentage of cases in which lesion or marker removal was confirmed at surgery was significantly higher in the cases in which a marker had been placed during the procedure (97%) than in cases in which a marker was not placed (23%). The findings at specimen radiography and histopathologic examination for the two groups are summarized in Table 1.

Specimen Histopathology
Histopathologic examination of the excised specimens revealed 47 of the 58 lesions (81%) localized with marker placement were benign, as were 51 of 77 lesions (66%) localized without marker placement. In the cases of all benign lesions, either a discrete finding or a healing biopsy site (when no discrete finding was present) was identified. Malignant lesions were identified in 19% of cases with marker placement and in 34% of cases without marker placement (Table 1).

None of the 11 malignant lesions localized with a marker had a positive inked surgical margin, in contrast to the 26 malignant lesions localized without a marker, two (8%) of which had a positive inked surgical margin (Table 1). The percentage of cases with close margins was similar for the two groups: 46% with marker placement and 31% without marker placement.

Table 2 shows the margin status of the various histopathologic subtypes of the malignant lesions localized with and without marker placement. In both the group with and the group without marker placement, six of the seven ductal carcinomas in situ (86%) and three of the six invasive lobular carcinomas (50%) had close or positive inked margins that necessitated reexcision. Only five of the 20 invasive ductal carcinomas (25%) and one of the four invasive carcinomas with ductal carcinoma in situ (25%) were found to have close or positive inked margins. However, the overall study sample size for malignant lesions was small, and these findings are not statistically significant. In addition, no significant difference in frequency of positive or close margins within the two groups was found among the histopathologic subtypes encountered at surgical excision (Table 2).


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TABLE 2: Histopathologic Subtypes of Malignant Lesions

 


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Specimen radiography or specimen sonography is performed after needle localization procedures to confirm surgical removal of the localized lesion. Specimen sonography is the preferred examination for surgical specimens initially localized with sonographic guidance [6]. However, in instances in which specimen sonography is not feasible, specimen radiography can be performed. The lack of proximity of the breast imaging center to the operating room can make specimen sonography logistically difficult if not impossible. In many instances, the lesion localized can be visualized with both mammography and sonography, and therefore specimen radiography can be performed to confirm surgical removal. However, it becomes difficult when the lesion being localized is not readily visualized with mammography; in those instances, specimen radiography probably will not be helpful.

We evaluated the benefit of placing a marker under sonographic guidance at needle localization to aid in identifying mammographically occult lesions within the specimen at surgical removal. As in our study, mammographically occult lesions can sometimes be visualized with specimen radiography, probably because of the decrease in tissue surrounding a lesion in specimens. In our study, only 18.5% of all mammographically occult lesions (25 of 135) were seen on specimen radiographs. In more than 80% of all cases, the specimen radiographs from needle localizations of these mammographically occult lesions did not confirm surgical removal of the lesions at surgery. The need for a technique that facilitated confirmation of appropriate surgical excision of these mammographically occult lesions became apparent. Placing a radiopaque marker at the site of the lesion under sonographic guidance at needle localization enables visualization of the localized site with specimen radiography when specimen sonography is not available.

In our study, confirmation of lesion or marker removal with specimen radiography was achieved at surgery 97% of the time when a marker was placed at needle localization versus 23% of the time when a marker was not placed. These results are similar to a reported 95.4% rate of lesion visualization achieved with specimen sonography [6]. Thus our findings show marker placement with specimen radiography for localization of mammographically occult lesions is a useful technique for confirmation of surgical removal of a lesion.

Improvement in margin status in cases of malignant lesions was achieved with a sonographic marker placement procedure. Clear inked margins were found in all cases in which a marker was placed, in contrast to 92% of cases in which a marker was not placed. However, there was no significant difference in the percentage of cases with positive or close margins necessitating reexcision. No differences in margin status were seen among the various histopathologic subtypes of malignant lesions localized with or without marker placement.

There are limitations to the sonographically guided marker placement procedure. Appropriate placement of the marker is important and must be at the exact site of the localized lesion. The procedure is typically easy and quick to perform but requires skill in sonographically guided procedures. In our study, all markers were placed at the lesion site, and placement was confirmed on follow-up mammograms showing the location of the marker with the adjacent localizing wire. A second limitation previously reported [9, 10] is marker migration after placement. Migration can occur while the patient travels from the breast imaging suite to the operating room. However, this time interval usually is small. Reported cases of marker migration have more commonly occurred over a period of days after the marker has been placed for percutaneous stereotactic biopsy and has moved owing to the accordion effect and bleeding, floating within a hematoma at the biopsy cavity, or resorption of air at the biopsy cavity [9]. Another limitation is cost added to the localizing procedure when a marker is used. The cost is minimal, however, in consideration of the larger cost of inadequate excision of a mammographically occult lesion during surgery.

Placement of a marker under sonographic guidance at needle localization is beneficial. It aids in identifying mammographically occult lesions within specimens and enables immediate confirmation of accurate surgical removal of localized lesions at surgical excision. Although there was a slight increase in the percentage of cases in which a clear inked margin was obtained, there was no appreciable difference in the percentage of cases with close or positive margins necessitating reexcision.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Jackson VP. The role of ultrasound in breast imaging. Radiology 1990;177 : 305–311[Free Full Text]
  2. Stavros AT, Thickman D, Rapp CL, Dennis MA, Parker SH, Sisney GA. Solid breast nodules: use of sonography to distinguish between benign and malignant lesions. Radiology 1995;196 : 123–124[Abstract/Free Full Text]
  3. Soo MS, Baker JA, Rosen EL, Vo TT. Sonographically guided biopsy of suspicious microcalcifications of the breast: a pilot study. AJR 2002; 178:1007 –1015[Abstract/Free Full Text]
  4. Parker SH, Burbank F. A practical approach to minimally invasive breast biopsy. Radiology 1996;200 : 11–20[Abstract/Free Full Text]
  5. Stomper PC, Davis SP, Sonnenfeld MR, Meyer JE, Greenes RA, Eberlein TJ. Efficacy of specimen radiography of clinically occult noncalcified breast lesions. AJR 1988;151 : 43–47[Abstract/Free Full Text]
  6. Mesurolle B, El-Khoury M, Hori D, et al. Sonography of postexcision specimens of nonpalpable breast lesions: value, limitations, and description of a method. AJR 2006;186 :1014 –1024[Abstract/Free Full Text]
  7. Nurko J, Mancino AT, Whitacre E, Edwards MJ. Surgical benefit conveyed by biopsy site marking system using ultrasound localization. Am J Surg 2005;190 : 618–622[CrossRef][Medline]
  8. Baron LF, Baron PL, Ackerman SJ, Durden DD, Pope TL. Sonographically guided clip placement facilitates localization of breast cancer after neoadjuvant chemotherapy. AJR2000; 174:539 –540[Free Full Text]
  9. Esserman LE, Cura MA, DaCosta DD. Recognizing pitfalls in early and late migration of clip markers after imaging-guided directional vacuum-assisted biopsy. RadioGraphics2004; 24:147 –156[Abstract/Free Full Text]
  10. Parikh JR. Delayed migration of gel mark ultra clip within 15 days of 11-gauge vacuum-assisted stereotactic breast biopsy. AJR 2005; 185:203 –206[Free Full Text]

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