2015
DOI: 10.1002/bjs.9884
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Nipple-sparing mastectomy in patients withBRCA1/2mutations and variants of uncertain significance

Abstract: Background Nipple-sparing mastectomy (NSM) is associated with improved cosmesis and is increasingly performed. Its role in BRCA mutation carriers has not been well described. Here indications and outcomes of BRCA mutation carriers undergoing NSM are studied. Methods BRCA mutations carriers who underwent NSM were identified. Details of patient demographics, surgical procedures, complications, and relevant disease stage and follow-up, were recorded. Results 177 NSMs were performed on 89 BRCA mutation carrier… Show more

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Cited by 77 publications
(43 citation statements)
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“…Here, nipple–areola complexes were preserved entirely in 378 mastectomies; only three required nipple excisions secondary to some degree of nipple–areola complex necrosis. The rate of nipple–areola complex necrosis in this study supports the premise that NSM can be performed with a low rate of necrosis similar to that reported in the literature.…”
Section: Discussionsupporting
confidence: 90%
“…Here, nipple–areola complexes were preserved entirely in 378 mastectomies; only three required nipple excisions secondary to some degree of nipple–areola complex necrosis. The rate of nipple–areola complex necrosis in this study supports the premise that NSM can be performed with a low rate of necrosis similar to that reported in the literature.…”
Section: Discussionsupporting
confidence: 90%
“…The panel recommended NSM for early breast cancer and ductal carcinoma in situ (DCIS), and, unanimously, in the risk reducing setting. This latter indication is now well-established in clinical practice [ 4 , 5 , 28 ].…”
Section: Resultsmentioning
confidence: 99%
“…However, they acknowledged that longer follow-up was needed. The 2015 study of manning et al [17] retrospectively assessed 728 NSMs in performed 413 patients between 2000 and 2013: 269 for breast cancer, 459 for risk reduction, and 177 (24.3%) in patients known to have a BRCA1/2 mutation, or a genetic variant of uncertain significance. No breast cancers were diagnosed over a median follow-up of 2.15 years (IQR 0.11-8.14).…”
Section: Nsm For Risk Reducingmentioning
confidence: 99%