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DOI:10.2214/AJR.06.1123
AJR 2007; 189:152-154
© American Roentgen Ray Society


Technical Innovation

CT-Guided Core Needle Biopsy of Breast Lesions Visible Only on MRI

Jeffrey B. Mendel1, Michelle Long1 and Priscilla J. Slanetz2

1 Department of Radiology, Caritas St. Elizabeth's Medical Center, 736 Cambridge St., Boston, MA 02135.
2 Department of Radiology, Boston Medical Center, Boston, MA.

Received August 22, 2006; accepted after revision January 26, 2007.

 
Address correspondence to J. B. Mendel (jeffrey.mendel{at}caritaschristi.org).


Abstract
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
OBJECTIVE. As breast MRI has become more widely used, the need to biopsy suspicious lesions visible only on MRI has increased. A small percentage of these lesions are not amenable to MR-guided biopsy. We report our technique of CT-guided core needle biopsy of breast lesions.

CONCLUSION. CT-guided core needle biopsy is a safe and effective method for sampling breast lesions visible only on MRI when MR-guided biopsy is not feasible.

Keywords: breast • breast biopsy • breast cancer • interventional radiology • MDCT • MRI • women's imaging


Introduction
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
MRI of the breast has emerged as a powerful imaging tool for the detection of clinically, sonographically, and mammographically occult breast cancers [1]. The indications for breast MRI continue to expand [2]. Although contrast-enhanced MRI has a high sensitivity for detecting breast carcinoma, the specificity is comparatively lower and the need to correlate MRI findings with histopathology exists [3].

With the increasing use of breast MRI, there is a need to accurately biopsy suspicious lesions that are mammographically and sonographically occult. Although various MR-guided core needle biopsy techniques have been developed, a small percentage of cases, because of lesion location, the presence of implants, or coexistent medical problems, are not amenable to MR-guided biopsy. Commonly, MR- or CT-guided needle localization procedures followed by excisional biopsy are used to sample these lesions [4].

Needle biopsy techniques have well-established advantages over surgical biopsies [5]. They are less invasive, less deforming to the breast, more cost effective, and quicker to perform than surgical biopsies and leave minimal visible scarring on subsequent mammograms. By adapting the techniques used for MR-guided biopsy, we can use CT-guided core needle biopsy to access these lesions, thereby avoiding the need for a surgical biopsy. In this report, we describe a technique that uses CT guidance to biopsy lesions detected on MRI when MR-guided biopsy is not practical.


Subjects and Methods
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
Institutional review board approval was waived because all CT-guided core needle biopsies were performed in the course of routine patient care. Informed consent was obtained from the patients, and data collection was compliant with the Health Insurance Portability and Accountability Act. Since December 2003, we have performed nine CT-guided breast biopsies in eight women. The mean age of these patients at biopsy was 56.7 years (range, 45-71 years). During the same time period at our institution, we performed 97 MR-guided breast biopsies, so CT-guided biopsy represented 9% of our overall cross-sectional imaging-guided breast biopsies.

Before biopsy, each patient underwent bilateral breast MRI using a 1.5-T system (Excite, GE Healthcare) and a dedicated breast coil (Breast Array Coil, InVivo). Our examination protocol consisted of unenhanced axial T1-weighted and STIR sequences; after the injection of 20 mL of nonionic contrast material (gadodiamide [Omniscan, GE Healthcare]) at a rate of 2 mL/s with a 20-mL saline flush using a dual syringe injector (Spectris, Medrad), dynamic contrast-enhanced axial fast acquisition with multiphase Efgre3D (enhanced fast gradient-echo 3D) (FAME) and contrast-enhanced sagittal FAME sequences were performed.

The areas of abnormal enhancement on MRI were identified using a dedicated workstation (DynaCAD, Invivo). Lesions ranged from 4 to 34 mm in the longest dimension, with a median size of 12 mm. Two lesions were ≤ 5 mm, two were 5-10 mm, and five were > 10 mm. All of the lesions were clinically, mammographically, and sonographically occult except one 34-mm lesion that was palpable. This lesion had previously undergone a biopsy without imaging guidance, but that biopsy yielded inconclusive results. MRI showed a localized area of suspicious enhancement that was occult on repeat mammography and sonography.


Figure 1
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Fig. 1A 70-year-old woman with history of treated ipsilateral breast cancer and suspicious enhancement in lateral aspect of breast. Biopsy revealed intracystic papilloma. MR image shows suspicious lesion (arrowhead) and MRI skin marker (arrow). Posterior margin of biopsy grid is indicated by thin white line.

 


Figure 2
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Fig. 1B 70-year-old woman with history of treated ipsilateral breast cancer and suspicious enhancement in lateral aspect of breast. Biopsy revealed intracystic papilloma. CT image obtained immediately after MRI shows lesion (arrowhead) is close to MRI skin marker (arrow).

 


Figure 3
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Fig. 2A 45-year-old woman with suspicious enhancement adjacent to breast implant. Pathology revealed benign breast tissue. MR image of suspicious lesion (arrowhead) and retropectoral breast implant (asterisk). MR-guided core needle biopsy could not be performed safely because projected path of biopsy needle (dotted line) would likely have ruptured implant. This image is rotated for comparison with B.

 


Figure 4
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Fig. 2B 45-year-old woman with suspicious enhancement adjacent to breast implant. Pathology revealed benign breast tissue. CT image shows lesion (arrowhead) and retropectoral breast implant (asterisk) with minimally radiopaque obturator in place (arrow).

 
MR-guided biopsy was attempted in two cases but was cancelled after the areas of enhancement were visualized posterior to the portion of the breast that is accessible using the biopsy grid (Fig. 1A). In these cases, an MRI marker was placed on the skin directly over the suspicious lesion and the position of the marker was confirmed using repeat MRI (Fig. 1A). The patient was then transferred to the CT scanner for a CT-guided biopsy (Fig. 1B). For the remaining seven lesions, MR-guided biopsy was not attempted for the following reasons: the lesion either was too superficial or could not be accessed using the biopsy grid, concomitant medical conditions precluded the patient from being prone for a prolonged period, or the projected biopsy path intersected with a saline implant (Fig. 2A).

For CT-guided biopsy, the patient was positioned supine with varying degrees of obliquity to optimize access to the lesion. A skin fiducial or paper grid (Fast Find Grid, E-Z-EM) was applied on the basis of the location of the lesion on MRI. The region of breast containing the abnormally enhancing tissue was scanned with 3-mm-thick CT slices obtained before and 150 seconds after the administration of 100 mL of nonionic contrast material (iohexol [Omnipaque 350, GE Healthcare]) injected at a rate of 2 mL/s with a 30-mL saline flush using a dual syringe injector (Stellant, Medrad) on a 16-MDCT scanner (Brilliance 16, Philips Medical Systems).

Scanning was originally performed using our standard chest CT technique (120 kVp, 300 mA). For later cases, patients were scanned with a lower-kilovoltage technique (90 kVp, 360 mA). Once the target was identified, the breast was prepared and draped in the usual sterile fashion and local anesthesia with 1% lidocaine hydrochloride was administered. A 3- to 4-mm skin incision was made with a number 11 blade at the entry site.

For large lesions that were unlikely to be obscured by the introducer sheath, the metal trocar needle and introducer sheath were inserted directly into the lesion. For artifact to be minimized, the trocar needle was then removed and a minimally radiopaque plastic obturator was inserted (Fig. 2B). Depending on the size and location of the lesion, between one and three CT series were needed to guide the trocar needle to its final position. Once correct positioning of the trocar needle was confirmed on CT, the obturator was removed and a vacuum-assisted biopsy device (ATEC, Suros Surgical Systems) was inserted into the sheath. Multiple samples were obtained with the device directed to ensure sampling of the region of interest. One biopsy was performed with an 18-gauge automated core biopsy needle (Temno, Cardinal Health) using a 17-gauge coaxial introducer needle. In this case, multiple passes were made to ensure adequate sampling.

For small lesions, a 25-gauge needle was inserted adjacent to the enhancing lesion (Fig. 3A). Given the inherent mobility of the breast, the small-gauge needle provided additional guidance during placement of the larger-gauge biopsy device.


Figure 5
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Fig. 3A 54-year-old woman with suspicious enhancement adjacent to chest wall. Pathology revealed invasive ductal carcinoma and ductal carcinoma in situ. CT image shows lesion (arrowhead) with 25-gauge guide needle (arrow) in place.

 
In four cases, by using a small-gauge needle as a guide, sonography was able to show lesions that had previously been occult on targeted breast sonography, allowing the use of adjunctive sonography during the biopsy (Fig. 3B). In the five cases in which sonography was used, a sonography unit equipped for breast imaging (Model 5000, Philips Medical Systems) was placed in the CT suite at the start of the CT procedure. Scanning was performed with 12- and 15-MHz linear transducers. All the lesions were nonspecific in sonographic appearance and were identified only after the small-gauge needle was inserted under CT guidance.


Figure 6
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Fig. 3B 54-year-old woman with suspicious enhancement adjacent to chest wall. Pathology revealed invasive ductal carcinoma and ductal carcinoma in situ. After CT-guided placement of guide needle (arrow), lesion (arrowhead) is faintly visible on sonography.

 

In all cases, a titanium marker (ATEC TriMark, Suros Surgical Systems) was deployed and CT was performed after the biopsy to ensure that the lesion was successfully sampled and the clip was correctly positioned. After the procedure, hemostasis was achieved with direct compression.


Results
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
Of nine lesions sampled using CT guidance, two were invasive ductal carcinoma, two showed atypical ductal hyperplasia (ADH), and the remaining five lesions were benign. For the two patients whose lesions were ADH at CT-guided biopsy, the final pathology results at surgical excision were ADH in one and chronic focal inflammation in the other. Follow-up MRI performed in three of the patients with benign biopsy results revealed no evidence of malignancy at a minimum of 18 months after biopsy. In all cases, the metallic marker was visualized on follow-up MRI. In one case, the marker had migrated slightly from the biopsy bed, but no residual enhancement was noted at the site of the original lesion. One patient died from unrelated causes 3 months after biopsy and one patient was lost to follow-up.


Discussion
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 
CT-guided percutaneous biopsy is a well-established technique in the chest, abdomen, and pelvis [6]. By adapting this technique and specific features from MR-guided breast biopsy, we have found a technique that offers a safe and effective way to sample those lesions for which MR-guided biopsy is not technically feasible. CT guidance is possible because the enhancement patterns seen with iodinated contrast material are similar to those observed with the use of gadolinium contrast material [4]. CT does not require the use of a breast coil or biopsy grid, so CT permits direct access to lesions anywhere within the breast. The biopsy path can be further tailored by adjusting the patient's position. CT facilitates patient monitoring and sedation, particularly when compared with MRI, which requires that patients be in the prone position. We performed most of our biopsies with a vacuum-assisted device to maximize the likelihood of successfully sampling small lesions. For large lesions, our technique was and can be used with an automated core biopsy device.

One challenge to our approach was breast mobility, a factor that is less problematic when using stereotactic, sonographic, or MRI guidance because each has an inherent ability to restrict motion. The initial placement of a thin needle helped by serving as a point of reference as the trocar needle was inserted. CT can potentially expose the breast to substantial radiation [7]. To minimize radiation dose, we limited the scans to the portion of the breast containing the lesion and did not obtain scout images. In later cases, we reduced the kilovoltage setting; this change yielded a fourfold radiation dose reduction with no apparent change in lesion conspicuity. Finally, the use of adjunctive sonography allowed the number of series per biopsy to be reduced by eliminating those series necessary to monitor both the insertion of the trocar needle and sheath and the successful sampling of the lesion.

In conclusion, CT-guided core needle biopsy can replace needle localization and surgical biopsy for a subset of MRI-detected, mammographically and sonographically occult lesions that are not amenable to conventional MR-guided biopsy due to lesion location or to other technical or patient factors.


References
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Abstract
Introduction
Subjects and Methods
Results
Discussion
References
 

  1. Buchanan CL, Morris EA, Dorn PL, Borgen PI, Van Zee KJ. Utility of breast magnetic resonance imaging in patients with occult primary breast cancer. Ann Surg Oncol 2005;12 : 1045-1053[CrossRef][Medline]
  2. Lalonde L, David J, Trop I. Magnetic resonance imaging of the breast: current indications. Can Assoc Radiol J2005; 56:301 -308[Medline]
  3. Olson JA Jr, Morris EA, Van Zee KJ, Linehan DC, Borgen PI. Magnetic resonance imaging facilitates breast conservation for occult breast cancer. Ann Surg Oncol 2000;7 : 411-415[CrossRef][Medline]
  4. Slanetz PJ, Jain R, Kline JL, et al. CT-guided preoperative needle localization of MR imaging-detected mammographically occult lesions. AJR 1999; 172:160 -162[Free Full Text]
  5. Liberman L. Centennial dissertation: percutaneous imaging-guided core breast biopsy—state of the art at the millennium. AJR 2000; 174:1191 -1199[Free Full Text]
  6. Grainger RG, Allison D, Adam A, Dixon AK, eds. Grainger and Allison's diagnostic radiology: a textbook of medical imaging, 4th ed. New York, NY: Churchill Livingstone, 2001:91 -92
  7. Hurwitz LM, Yoshizumi TT, Reiman RE, et al. Radiation dose to the female breast from 16-MDCT body protocols. AJR2006; 186:1718 -1722[Abstract/Free Full Text]

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This Article
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