Abstract
Accurate location of small breast lesions is mandatory for proper surgical management. The purpose of this article is systematically review procedures used to locate non-palpable breast lesions, including a description of the current status, advantages, and disadvantages for each technique. A total of 47 articles were finally included: 7 articles for the wire location technique, 5 articles for the radioguided location technique, 13 articles that compare wire location with radioguided location, 3 articles for the carbon location technique, 2 articles that compare wire location with carbon location, and 17 articles for the clip location technique. The success of location and the clear margin are reported for each location technique and for the separate articles included; clip migration shift, also, is reported for the clip location technique. Odds ratio with related 95 % confidence intervals were also calculated for successful location. Comparative analysis or meta-analysis for all the different breast lesion location techniques is missing. Prospective investigations and randomized investigations for homogeneous populations are still needed to determine which is the most cost-effective modality among those used to date.
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Avoid common mistakes on your manuscript.
Background
With the worldwide introduction of mammographic screening programs and with women’s increased awareness, small non-palpable breast lesions, usually smaller than 1 cm, are being detected with increasing frequency. Up to 25 % of breast lesions visualized by mammography or sonography are clinically non-palpable (i.e. not detectable by physical examination even if performed by an expert physician and based on topographic imaging data) (Table 1). Thus, appropriate management of non-palpable breast lesions has become an important issue with socioeconomic and emotional implications, moreover 9–63 % of these abnormalities are eventually found to be malignant [1] (Table 2).
It is necessary to accurately locate such occult lesions, with the objective of excising the smallest amount of tissue and yet to remove the entire lesion whilst achieving adequate clear margins. Location of the lesions is useful for radical resection of the tumor to:
-
provide a correlation of biopsied lesions revealed both by sonography and mammography [5, 6];
-
locate the tumor bed in a locally advanced cancer patient after receiving preoperative neoadjuvant chemotherapy (given the frequently encountered marked response to treatment) [7, 8], and
-
assess, after a stereotactic, vacuum-assisted breast biopsy, the accuracy of marker clip deployment for guiding subsequent needle location procedures and surgery [9].
Several techniques have been described for preoperative location, including wire-located breast biopsy (WL), radioguided occult location (ROLL), clip location, and carbon location (CL). Other authors have already published reviews on techniques for location of breast lesions. Jakub et al. [10] reviewed the current status of radioactive seed location. Van der Ploeg et al. [11] and Lovrics et al. [12] have written reviews comparing ROLL and WL but without taking other modalities in consideration. The purpose of our study was to report all the techniques proposed for location of breast lesions, analyzing their current status and their advantages and disadvantages.
Methods
Search strategy and selection criteria
This study was approved by the ethics on research committee of our institution “National Cancer Institute of Naples IRCCS Pascale Foundation”. Data for this review were identified by searches of the Pubmed database using a multimodal strategy and the search terms: breast clip placement or location, wire breast location, carbon breast location, radio-guided occult breast or seed location, titanium breast location, titanium or collagen or radiopaque clip breast location.
The inclusion criteria were: clinical study evaluating wire location, radio-guided location, carbon location, or clip location technique for non-palpable breast lesions; the presence of a criterion of performance evaluation for the considered breast location techniques; and availability of the full text. Only papers published in the English language from January 1987 to February 2011 were included. The references of these studies were also analyzed to identify original studies that were not identified by the search of the data. Exclusion criteria were: palpable tumors only included, not full text and not original research article type (abstract, editorial, case report, or review), and lack of reporting of clear margin status, of diagnostic success, or of clip migration.
Evaluation of outcomes
Comparisons among the several location techniques were conducted by choosing papers that reported the outcomes: successful location, clear margins, and clip migration (the last for the clip location technique only).
Successful location corresponded to the percentage of locations that did not fail. Causes of procedure failure typically include displacement of the location wire during surgery, deeply placed/relatively inaccessible lesion; lesion poorly defined in comparison with the surrounding breast tissue, and large breast size [13]. Another outcome considered was the percentage of clear margins after surgery. In accordance with the criteria defined by Solin et al. [14], a surgical margin is regarded as clear when at least 2 mm of normal breast tissue surround the carcinoma, as close when less than 2 mm of normal breast tissue surround the carcinoma, and as involved when carcinoma was found in the surgical margins. For the clip location technique another outcome was used—migration of the marker from the initial site expressed in centimeters. Values were reported as average ± standard deviation.
The odds ratio is a measure of effect size, describing the strength of association or non-independence between two binary data values. An odds ratio is a measure of association between an exposure and an outcome. The 95 % CI is used to estimate the precision of the odds ratio. A large CI indicates a low level of precision of the odds ratio, whereas a small CI indicates a higher precision of the OR [84]. In this study the odds ratio with the related 95 % CI was used to compare successful location for each location technique and the effect size for each considered study in the review. The odds ratio was reported for successful location only, because for the clip location techniques a few articles report this outcome.
A P value <0.05 was considered significant. All analyses were performed using Statistic Toolbox of Matlab R2007a (The Math-Works, Natick, MA, USA).
Results
A Pubmed search yielded 55 articles for key breast clip placement or location, 299 articles for wire location, 34 articles for CL, 36 articles for ROLL, 23 articles for seed location, and 35 articles for titanium, radiopaque, collagen clip location. Three-hundred and ninety-one articles were regarded as irrelevant and excluded because they did not correspond to the topic of interest. Ninety-one articles were read and evaluated on the basis of the inclusion and exclusion criteria defined in the “Methods” section. A total of 47 articles were included in this systematic review: 7 for the wire location technique, 5 for the ROLL technique, 13 comparing wire location with radioguided location, 3 for the CL technique, 2 comparing wire location with CL, and 17 for the clip location technique. No overtly duplicated article was found (Fig. 1).
In Fig. 2, in which several location techniques are compared, the sizes of the circles represent the number of lesions studied by each technique. The most frequently used location technique was WL (43 % of studies); ROLL was used in 17 % of articles, CL in 14 %, and clip location in 25 %.
Table 3 shows reported diagnostic success and clear margins, both as percentages, for wire location, radioguided location, and CL. The range of successful location for the WL technique was 65–100 % (53.9 ± 46.6 %) and the range for clear margins was 58–84 % (50.9 ± 29.2 %). The range of successful location for ROLL was 93–100 % (54.9 ± 50.5 %) and the range for clear margins was 60–100 % (78.4 ± 22.4 %). The range of successful location for CL was 79–99 % (90.8 ± 7.4 %) and the range for clear margins was 75–81 % (78.0 ± 4.3 %). Table 4 shows diagnostic success and clip migration less than 1 cm, both as percentages, for the clip location technique. The range of successful location was 80–100 % (95.4 ± 7.6 %) and the range for clip shift <1 cm was 56–100 % (66.7 ± 39.8 %).
High odds ratios indicate reduced risk of unsuccessful location using each method. High variability of the odds ratios and 95 % confidence intervals for the different studies reported reveal heterogeneity of successful location.
Discussion
Successful management of non-palpable lesions depends on accurate location, which is essential for achieving complete surgical excision with optimum cosmesis and minimum morbidity. A variety of imaging techniques and labeling materials are available for location of non-palpable lesions.
Imaging guidance is performed by use of mammography (stereotactic biopsy) or sonography and less often by use of magnetic resonance imaging (MRI). In general terms, the choice of guidance tool depends on the characteristics of the lesion and on radiologist preference.
Core biopsy guided by stereotactic mammography is the most common technique used for investigation, location, and sampling of non-palpable suspicious mammographic lesions. Mammographic location methods differ in technical requirements, duration, and precision. Stereotaxis reduces the time from mammographic detection to treatment; it results in significant cost savings compared with open biopsy, and is an accurate and less invasive method [15]. However, because, to obtain the views, limited compression is necessary, perfectly orthogonal images cannot be obtained and, consequently, perfect location is not achievable [15]. Sonography is an important adjunct to mammography and clinical examination of breast lesions. Limitations include poor results for fatty breasts, inability to depict microcalcifications, and excessive scan and review time [16]. Ultrasound guidance is simple and safe, and is preferable to other methods whenever feasible [16–18]. MRI is a relatively new technique and few reports have been published. Disadvantages such as overlap of MRI features of malignant and benign lesions, high cost, and inability to resolve smaller masses and microcalcifications have been described [19]. MRI has been used to evaluate multicentricity or multifocality of breast cancer detected by other methods, locate mammographically occult cancer in women with axillary metastases, evaluate treatment response during neoadjuvant chemotherapy, and identify breast cancer in high-risk patients [20–22]. MRI can furnish important information that cannot be obtained by conventional mammography or physical examination and may detect cancer that is mammographically, ultrasonographically, and clinically occult [9, 23, 24]. Therefore, for lesions detected with MRI that cannot be visualized with other methods, MR-guided intervention is necessary if tissue diagnosis is required. MR-guided wire location followed by excision biopsy is still the mainstay of MR-guided intervention, although an increasing number of investigators use MR-guided vacuum-assisted core-needle biopsy of the breast to yield tissue for diagnosis [25]. Walf et al. reported that wire location of the lesion with MRI was efficient and reliable for non-palpable lesions only visible on MRI by use of a non-dedicated body coil [26].
Whatever the guidance tool used, the most diffuse and standardized modality of preoperative location of non-palpable lesions is WL. There are several well-described disadvantages of WL, however, for example wire incidental migration, kinking, and fracture [10, 27, 28]. Microscopic margins may be positive, requiring additional operations: 20–50 % of excisions are reported as incomplete [10]. Furthermore, because it is advised that hookwire location is performed on the same day as surgery to prevent migration, there may be logistical problems between the radiological, surgical, and nuclear medicine departments: the surgeon is often unable to confirm the exact site of the lesion in the breast; scheduling conflicts between the surgeon and the radiologist can occur, resulting from the need to coordinate multiple procedures on the same day with different teams; and there is an inability to use wire location for the first start time in the morning without a significant delay in the operating room.
Several location techniques alternative to WL and a variety of markers have been described by different authors [29–33]. ROLL is a useful method for detection of non-palpable lesions by injection of a nuclear tracer (99m Tc-labeled colloidal albumin) directly around the tumor. Excision of the primary tumor is guided by a hand-held gamma probe. A sentinel lymph-node excision biopsy can be performed at the same time, if needed [34–36]. ROLL is a fast, safe, and effective method for identifying and removing subclinical breast lesions. Compared with WL, the volume of breast parenchyma removed is smaller, there is better centering of the lesion within the surgical specimen, and the cosmetic results are better because skin incision and breast dissection are determined by the surgeon, irrespective of any wire positioning [37]. Another radioguided location procedure, termed breast seed location, uses a titanium capsule containing iodine 125 [38]. Radioactive seeds may be placed up to 3 days before surgical intervention, enabling the radiology and surgical schedules to remain independent, thereby increasing operating suite efficiency and optimizing the schedule of the mammographer and the surgeon. Studies using these seeds, as an alternative to WL, revealed significant reduction in re-excisions to obtain negative margins and elimination of need for specimen mammograms [10]. However, seeds have the disadvantages of requiring a location procedure on a separate occasion from the percutaneous needle biopsy and of requiring expensive and specialized radiopharmaceuticals.
Carbon location (CL) is another procedure, first reported in 1983 [39]. This technique involves placement of an inert carbon tract, which stains the tissue black in color, does not diffuse into the surrounding tissue, and can be used by the surgeon to locate the lesion days or weeks later. Insertion of the carbon track immediately after needle biopsy adds only 5 min to the procedure. It is used in some parts of the world [40, 41] but has not been widely reported and its effectiveness has not been compared with that of the hookwire [30]. Without CL, deployment of a titanium clip is required to enable subsequent mammographic location. In these circumstances, a carbon track is less expensive than a titanium clip, a post-procedure mammogram is unnecessary, because of the carbon map success, and an additional locating procedure is avoided. CL with stereotaxis is useful for lesions in which the mammographic abnormality is revealed in one projection only, rendering hookwire location virtually impossible. There are cases in which CL suffers from technical difficulties. Needle and syringe port blockage by carbon particles is not uncommon when the carbon is injected vertically, and this limits the utility of add-on stereotactic devices [30]. If the lesion is close to the chest wall, particularly in a large breast, there is a danger that a long carbon track will be difficult for the surgeon to follow and a hookwire may be preferable. For extensive or multifocal lesions several carbon tracks are difficult to follow. In the rare event a lesion is missed, it is usually relocated with hookwire, because the hematoma in the cavity can interfere with recognition of the carbon. CL has advantages and disadvantages for the pathologist. The main advantage is that the carbon track can be used to locate the lesion in the specimen. There is scope for CL to be used before total mastectomy, especially for large breasts or when mastectomy is being performed for synchronous or very small cancers. The disadvantages are that the carbon tracks resist slicing and the carbon can distort or obscure the lesion. To avoid this, the carbon should be injected only as far as the edge of the lesion [30].
Placement of marker clips can be used to indicate the biopsy site as part of image-guided breast procedures. The objective is to mark the tumor bed, thus enabling accurate needle location at the time of definitive surgery in the event of complete mammographic and sonographic resolution of the tumor [31, 32]. Markers are usually small stainless-steel clips prone to pinching a minute amount of breast tissue (e.g. MicroMark; Ethicon Endosurgery, Cincinnati, OH, USA). However, the clip may fail to hold on to the tissue or the clip may migrate to a different, undesired, location. New markers have been developed, for example clips included in pellets of a copolymer of resorbable polylactic acid and polyglycolic acid (Gel Mark, Gel Mark Ultra and Gel Mark UltraCor; SenoRx, Aliso Viejo, CA, USA) or titanium clips that are embedded centrally on a collagen plug (Mammomark; Artemis, Hayward, CA, USA) or a radiopaque titanium metal ring surrounding a bioabsorbable collagen cylinder (Vivant Medical Biopsy Marker; Vivant Medical, Mountain View, CA, USA), or a desiccated hydrogel embedded with either a stainless steel or titanium coil (Hydromark; Biopsy Sciences, Clearwater, FL, USA). For the first, clip migration has been described in case reports [21, 42]. The collagen plug marking device might be an effective alternative to existing marker clips [43]. After deployment of the marking device, the collagen expands as it absorbs fluid and stabilizes the marker within the cavity. Theoretically, this feature tends to place the metallic marker centrally in the biopsy cavity and makes the marker resistant to migration. Also there is a potential hemostatic benefit from the collagen because it promotes haemostasis [44]. However, there are several published data on the deployment accuracy of these clips (Table 4). Rosen et al. [22] and Uematsu et al. [45] reported clip placement >1 cm in 28 % of the cases, as determined by comparing the coordinates of the clip and those of the original target on the stereotactic images. Burbank and Forcier [46] determined their initial clip placement accuracy (89–93 %) on the basis of the mask measurement system by using mammograms obtained before and after biopsy. There are many reported causes of clip migration. The clip is deployed at the end of the stereotactic biopsy, with the breast compressed in the cranio-caudal or lateral plane. However, when compression is released, the breast expands to its original shape and size and the clip can migrate in the direction of compression, which is along the direction of the needle track (Z axis). Other mechanisms of migration include: clip migration in the biopsy track, clip floating in a hematoma, clip displacement by a hematoma, change in clip site because of resorption of air at the biopsy cavity, and change in clip site after surgery, chemotherapy, or radiation therapy [47, 48]. Results suggest that the position of metallic clips placed during stereotactic core needle biopsy may differ substantially from the location of the biopsy site [1]. For a marker to be useful, it must remain close to the biopsy site. Studies of the accuracy of clip deployment show that 72–98 % of clips are <1 cm from the target [13, 22].
Conclusions
In conclusion, a variety of location techniques are currently used to assist the breast surgeon in achieving complete removal of the nodules/calcification clusters and achieving clear histological margins. Each modality has its advantages and disadvantages. The published literature basically lacks comparative analysis or meta-analysis of all the different breast lesion-location techniques by means of prospective randomized studies on a homogeneous population, and the high variability of odds ratio and 95 % confidence intervals in different reported studies shows the heterogeneity of successful location. Moreover, although the absence of comparative studies does not enable recommendation of one of the techniques discussed, certainly a promising technique, considering high mean successful location and clear margin, is clip location.
Abbreviations
- CI:
-
Confidence interval
- CL:
-
Carbon location
- MRI:
-
Magnetic resonance imaging
- ROLL:
-
Radioguided occult location
- WL:
-
Wire location
References
Ernst MF, Avenarius JKA, Schuur KH, et al. Wire localization of non-palpable breast lesions: out of date? Breast. 2002;11:408–13.
Chu TYC, Lui CY, Hung WK, et al. Localisation of occult breast lesion: a comparative analysis of hookwire and radioguided procedures. Hong Kong Med J. 2010;16:367–72.
van Riet YEA, Jansen FH, van Beek M, et al. Localization of non-palpable breast cancer using a radiolabelled titanium seed. Br J Surg. 2010;97:1240–5.
Liberman L, Kaplan J, Van Zee KJ, et al. Bracketing wires for preoperative breast needle localization. AJR. 2001;177:565–72.
Guenin MA. Clip placement during sonographically guided large-core breast biopsy for mammographic-sonographic correlation. AJR. 2000;175:1053–5.
Malvica RP. Sonographic location of the elusive breast lesion: a technical aid to stereotaxic large-needle core biopsy. AJR. 1996;167:183–4.
Oh JL, Nguyen G, Whitman GJ, et al. Placement of radiopaque clips for tumor localization in patients undergoing neoadjuvant chemotherapy and breast conservation therapy. Cancer. 2007;110:2420–7.
Edeiken BS, Fornage BD, Bedi DG, et al. US-guided implantation of metallic markers for permanent localization of the tumor bed in patients with breast cancer who undergo preoperative chemotherapy. Radiology. 1999;213:895–900.
Kruger BM, Burrowes P, MacGregor JH. Accuracy of marker clip placement after mammotome breast biopsy. Can Assoc Radiol J. 2002;53:137–40.
Jakub JW, Gray RJ, Degnim AC, et al. Current status of radioactive seed for localization of non palpable breast lesions. Am J Surg. 2010;199:522–8.
Van der ploeg I, Hobbelink M, Vandenbosch M, et al. Radioguided occult lesion localisation (ROLL) for non-palpable breast lesions: a review of the relevant literature. Eur J Surg Oncol. 2008;34:1–5.
Lovrics PJ, Cornacchi SD, Vora R, et al. Systematic review of radioguided surgery for non-palpable breast cancer. Eur J Surg Oncol. 2011;37:388–97.
Genson CC, Blane CE, Helvie MA, et al. Effects on breast MRI of artifacts caused by metallic tissue marker clips. AJR. 2007;188:372–6.
Solin LJ, Yeh I, Kurtz J, et al. Ductal carcinoma in situ (intraductal carcinoma) of the breast treated with breast-conserving surgery and definitive irradiation correlation of pathologic parameters with outcome of treatment. Cancer. 1993;71:2532–42.
Parker SH, Lovin JD, Jobe WE, et al. Stereotactic breast biopsy with a biopsy gun. Radiology. 1990;176:741–7.
Weber WN, Sickles EA, Callen PW, et al. Nonpalpable breast lesion localization: limited efficacy of sonography. Radiology. 1985;155:783–4.
Caruso M, Gabrieli G, Marzullo G, et al. Core biopsy as alternative to fine-needle aspiration biopsy in diagnosis of breast tumors. Oncologist. 1998;3:45–9.
Roux S, Logan-Young W. Private practice interdisciplinary breast centers: their rationale and impact on patients, physicians, and the health care industry: a bicoastal perspective. Surg Oncol Clin North Am. 2000;9:177–98.
Ross RJ, Thompson JS, Kim K, et al. Nuclear magnetic resonance imaging and evaluation of human breast tissue: preliminary clinical trials. Radiology. 1982;143:195–205.
Orel SG, Schnall MD. MR imaging of the breast for the detection, diagnosis, and staging of breast cancer. Radiology. 2001;220:13–30.
Philpotts LE, Lee CH. Clip migration after 11-gauge vacuum-assisted stereotactic biopsy: case report. Radiology. 2002;222:794–6.
Rosen EL, Vo TT. Metallic clip deployment during stereotactic breast biopsy: retrospective analysis. Radiology. 2001;218:510–6.
Perlet C, Sittek H, Reiser M, et al. Clip marker placement following MR-guided vacuum biopsy of the breast. Radiologe. 2005;45:230–6.
Kubota K, Gomi N, Wakita T, et al. Magnetic resonance imaging of the metal clip in a breast: safety and its availability as a negative marker. Breast Cancer. 2004;11:55–9.
Gossmann A, Bangard C, Warm M, et al. Real-time MR-guided wire localization of breast lesions by using an open 1.0-T imager: initial experience. Radiology. 2008;247:535–42.
Wolf G, Helbich T. Results of stereotactic guidance of breast excisional biopsy versus stereotactic core biopsy in occult breast lesions. Wien Med Wochenschr. 1998;148:316–20.
Montrey J, Levy J, Brenner R. Wire fragments after needle localization. AJR. 1996;167:1267–9.
Bronstein AD, Kilcoyne RF, Moe RE. Complications of needle localization of foreign bodies and nonpalpable breast lesions. Arch Surg. 1988;123:775–9.
Intra M, Cicco C, Gentilini O, et al. Radioguided localisation (ROLL) of non-palpable breast lesions and simultaneous sentinel lymph node biopsy (SNOLL): the experience of the European Institute of Oncology. Eur J Nucl Med Mol Imaging. 2007;34:957–8.
Rose A, Collins JP, Neerhut P, et al. Carbon localisation of impalpable breast lesions. Breast. 2003;12:264–9.
Baron LF, Baron PL, Ackerman SJ, et al. Sonographically guided clip placement facilitates localization of breast cancer after neoadjuvant chemotherapy. AJR. 2000;174:539–40.
Dash N, Chafin SH, Johnson RR, et al. Usefulness of tissue marker clips in patients undergoing neoadjuvant chemotherapy for breast cancer. AJR. 1999;173:911–7.
Mariscal Martinez A, Sola M, de Tudela AP, et al. Radioguided localization of nonpalpable breast cancer lesions: randomized comparison with wire localization in patients undergoing conservative surgery and sentinel node biopsy. AJR. 2009;193:1001–9.
Luini A, Zurrida S, Paganelli G, et al. Comparison of radioguided excision with wire localization of occult breast lesions. Br J Surg. 1999;86:522–5.
Medina-Franco H, Abarca-Prez L, Garca-Alvarez MN, et al. Radioguided occult lesion localization (ROLL) versus wire-guided lumpectomy for non-palpable breast lesions: a randomized prospective evaluation. J Surg Oncol. 2008;97:108–11.
Aydogan F, Ozben V, Celik V, et al. Radio-guided occult lesion localization (ROLL) for non-palpable breast cancer: a comparison between day-before and same-day protocols. Breast. 2010;19:226–30.
Nadeem R, Chagla LS, Harris O, et al. Occult breast lesions: a comparison between radioguided occult lesion localisation (ROLL) vs. wire-guided lumpectomy (WGL). Breast. 2005;14:283–9.
Rao R, Moldrem A, Sarode V, et al. Experience with seed localization for nonpalpable breast lesions in a public health care system. Ann Surg Oncol. 2010;17:3241–6.
Svane G. A stereotaxic technique for preoperative marking of non-palpable breast lesions. Acta Radiol. 1983;24:145–51.
Canavese G, Catturich A, Vecchio C, et al. Pre-operative localization of non-palpable lesions in breast cancer by charcoal suspension. Eur J Surg Oncol. 1995;21:47–9.
Mazy S, Galant C, Berlire M, et al. Localization of non-palpable breast lesions with black carbon powder (experience of the Catholic University of Louvain). J Radiol. 2001;82:161–4.
Parikh JR. Delayed migration of gel mark ultra clip within 15 days of 11-gauge vacuum-assisted stereotactic breast biopsy. AJR. 2005;185:203–6.
Rosen EL, Baker JA, Soo MS. Accuracy of a collagen-plug biopsy site marking device deployed after stereotactic core needle breast biopsy. AJR. 2003;181:1295–9.
Kass R, Kumar G, Klimberg VS, et al. Clip migration in stereotactic biopsy. Am J Surg. 2002;184:325–31.
Uematsu T, Kasami M, Takahashi K, et al. Clip placement after an 11-gauge vacuum-assisted stereotactic breast biopsy: correlation between breast thickness and clip movement. Breast Cancer. 2011 (Epub ahead of print).
Burbank F, Forcier N. Tissue marking clip for stereotactic breast biopsy: initial placement accuracy, long-term stability, and usefulness as a guide for wire localization. Radiology. 1997;205:407–15.
Esserman LE, Cura MA, DaCosta D. Recognizing pitfalls in early and late migration of clip markers after imaging-guided directional vacuum-assisted biopsy. RadioGraphics. 2004;24:147–56.
Harris AT. Clip migration within 8 days of 11-gauge vacuum-assisted stereotactic breast biopsy: case report. Radiology. 2003;228:552–4.
Cho KR, Seo BK, Lee J, et al. A comparative study of palpable and nonpalpable breast cancers determined by ultrasonography. J Breast Cancer. 2008;11:64–70.
Berg WA, Gutierrez L, Nessaiver MS, et al. Diagnostic accuracy of mammography, clinical examination, US, and MR imaging in preoperative assessment of breast cancer. Radiology. 2004;233:830–49.
Londero V, Zuiani C, Furlan A, et al. Role of ultrasound and sonographically guided core biopsy in the diagnostic evaluation of ductal carcinoma in situ (DCIS) of the breast. Radiol Med. 2007;112:863–76.
Bassett L, Liu T, Giuliano A, et al. The prevalence of carcinoma in palpable vs impalpable, mammographically detected lesions. AJR. 1991;157:21–4.
Barros ACSD, Barros MAC, Andrade FE, et al. Combined radioguided nonpalpable lesion localization and sentinel lymph node biopsy for early breast carcinoma. Ann Surg Oncol. 2007;14:1472–7.
Chen B, Liu C, Jin F, et al. The role of fine-wire localization breast biopsy in the management of BI-RADS category 3–5 non-palpable breast lesions in northeastern Chinese women. Health. 2010;2:291–4.
Chen X, Lehman CD, Dee KE. MRI-guided breast biopsy: clinical experience with 14-gauge stainless steel core biopsy needle. AJR. 2004;182:1075–80.
Gisvold JJ, Martin JK. Prebiopsy localization of nonpalpable breast lesions. AJR. 1984;143:477–81.
Landheer ML, Veltman J, van Eekeren R, et al. MRI-guided preoperative wire localization of nonpalpable breast lesions. Clin Imaging. 2006;30:229–33.
Ng CH, Lee KT, Taib NA, et al. Experience with hookwire localisation excision biopsy at a medical centre in Malaysia. Singapore Med J. 2010;51:306–10.
Lehman CD, Shook JE. Position of clip placement after vacuum-assisted breast biopsy: is a unilateral two-view postbiopsy mammogram necessary? Breast J. 2003;9:272–6.
Liberman L, Bracero N, Morris E, et al. MRI-guided 9-gauge vacuum-assisted breast biopsy: initial clinical experience. AJR. 2005;185:183–93.
Phillips SW, Gabriel H, Comstock CE, et al. Sonographically guided metallic clip placement after core needle biopsy of the breast. AJR. 2000;175:1353–5.
Chadwick DR, Shorthouse AJ. Wire-directed localization biopsy of the breast: an audit of results and analysis of factors influencing therapeutic value in the treatment of breast cancer. Eur J Surg Oncol. 1997;23:128–33.
Allen MJ, Thompson WD, Stuart RC, et al. Management of non-palpable breast lesions detected mammographically. Br J Surg. 1994;81:543–5.
Gray RJ, Pockaj BA, Karstaedt PJ, et al. Radioactive seed localization of nonpalpable breast lesions is better than wire localization. Am J Surg. 2004;188:377–80.
Moss HA, Barter SJ, Nayagam M, et al. The use of carbon suspension as an adjunct to wire localisation of impalpable breast lesions. Clin Radiol. 2002;57:937–44.
Arman A, Kilicoglu G, Guner HH, et al. Marking of nonpalpable breast lesions using a custom carbon suspension. Acta Radiol. 2001;42:599–601.
Chen X, Lehman CD, Dee KE. MRI-guided breast biopsy: clinical experience with 14-gauge stainless steel core biopsy needle. AJR. 2004;182:1075–80.
Thind C, Desmond S, Harris O, et al. Radio-guided localization of clinically occult breast lesions (ROLL): a DGH experience. Clin Radiol. 2005;60:681–6.
Ronka R, Krogerus L, Leppnen E, et al. Radio-guided occult lesion localization in patients undergoing breast-conserving surgery and sentinel node biopsy. Am J Surg. 2004;187:491–6.
Zgajnar J, Hocevar M, Frkovic-Grazio S, et al. Radioguided occult lesion localization (ROLL) of the nonpalpable breast lesions. Neoplasma. 2004;51:385–9.
Gray RJ, Salud C, Nguyen K, et al. Randomized prospective evaluation of a novel technique for biopsy or lumpectomy of nonpalpable breast lesions: radioactive seed versus wire localization. Ann Surg Oncol. 2001;8:711–5.
Riedl CC, Pfarl G, Helbich TH, et al. Comparison of wire versus carbon localization of non-palpable breast lesions. RöFo. 2002;174:1126–31.
Moreno M, Wiltgen JE, Bodanese B, et al. Radioguided breast surgery for occult lesion localization—correlation between two methods. J Exp Clin Cancer Res. 2008;27:29.
Rampaul RS, Bagnall M, Burrell H, et al. Randomized clinical trial comparing radioisotope occult lesion localization and wire-guided excision for biopsy of occult breast lesions. Br J Surg. 2004;91:1575–7.
Hughes JH, Mason MC, Gray RJ, et al. A multi-site validation trial of radioactive seed localization as an alternative to wire localization. Breast J. 2008;14:153–7.
Belloni E, Canevari C, Panizza P, et al. Nonpalpable breast lesions: preoperative radiological guidance in radioguided occult lesion localisation (ROLL). Radiol med. 2011;116(4):564–74.
Smathers RL. Marking the cavity site after stereotactic core needle breast biopsy. AJR. 2003;180:355–6.
Parker SH, Kaske TI, Gerharter JE, Dennis MA, Chavez JL. Placement accuracy and ultrasonographic visualization of a new percutaneous breast biopsy marker. Radiology. 2001;221(P):431.
Esserman LE, Costa D, Kusnick CA, Lowers K. Placement of a new ultrasound (US) visible breast biopsy marker in US-guided 11 gauge directional vacuum assisted biopsy (DVAB) (abstr). Radiology. 2002;25(P):459.
Margolin FR, Kaufman L, Denny SR, et al. Metallic marker placement after stereotactic core biopsy of breast calcifications: comparison of two clips and deployment techniques. AJR. 2003;181:1685–90.
Liberman L, Hann LE, Dershaw DD, et al. Mammographic findings after stereotactic 14-gauge vacuum biopsy. Radiology. 1997;203:343–7.
Coles CE, Wilson CB, Cumming J, et al. Titanium clip placement to allow accurate tumour bed localisation following breast conserving surgery: audit on behalf of the IMPORT Trial Management Group. Eur J Surg Oncol. 2009;35:578–82.
Feggi L, Basaglia E, Corcione S, et al. An original approach in the diagnosis of early breast cancer: use of the same radiopharmaceutical for both non-palpable lesions and sentinel node localisation. Eur J Nucl Med. 2001;28(11):1589–96.
Cornfield J. A method for estimating comparative rates from clinical data. Applications to cancer of the lung, breast, and cervix. J Natl Cancer Inst. 1951;11:1269–75.
Acknowledgments
The authors are grateful to Alessandra Trocino, librarian at the National Cancer Institute “G. Pascale” of Naples, Italy, for bibliographic assistance.
Conflict of interest
The authors declare that they have no competing interests. The authors have no conflict of interest to be disclosed.
Author contribution
RF works on literature search, statistical analysis and drafting of the manuscript in collaboration with AP. OC,VG and SF participated in the drafting the manuscript. MS participated in the design of the study and performed the statistical analysis. MD, QP and MDA conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
Author information
Authors and Affiliations
Corresponding author
Additional information
R. Fusco and A. Petrillo contributed equally to this work.
About this article
Cite this article
Fusco, R., Petrillo, A., Catalano, O. et al. Procedures for location of non-palpable breast lesions: a systematic review for the radiologist. Breast Cancer 21, 522–531 (2014). https://doi.org/10.1007/s12282-012-0427-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12282-012-0427-1