2021
DOI: 10.1016/j.gore.2021.100795
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Ovarian cancer arising from the proximal fallopian tube in a patient with a BRCA2 mutation

Abstract: Highlights BRCA1/2 carriers are at high risk for fallopian tube carcinoma, which can arise in the proximal fallopian tube. Pathologic analysis of RRBSO specimens should include serial sectioning of the entire tube, not just the fimbriated end. Concurrent hysterectomy at time of RRBSO may be considered to ensure all tubal epithelium is resected.

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Cited by 2 publications
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“…High-grade serous ovarian carcinoma has been associated with STIC/STIL with multiple lesions in the fimbria, older age, and many p53 signatures (benign-appearing tubal epithelium with a p53 mutation) [ 3 ]. The current theory of HGSOC pathogenesis starts with fallopian tube secretory cell outgrowth (SCOUT) and progresses through the p53 signature to STILs and STICs [ 4 ]. It is believed that STIC cells detach from the fallopian tube surface and disseminate to the ovaries and peritoneal tissue, where masses are formed [ 3 ].…”
Section: Discussionmentioning
confidence: 99%
“…High-grade serous ovarian carcinoma has been associated with STIC/STIL with multiple lesions in the fimbria, older age, and many p53 signatures (benign-appearing tubal epithelium with a p53 mutation) [ 3 ]. The current theory of HGSOC pathogenesis starts with fallopian tube secretory cell outgrowth (SCOUT) and progresses through the p53 signature to STILs and STICs [ 4 ]. It is believed that STIC cells detach from the fallopian tube surface and disseminate to the ovaries and peritoneal tissue, where masses are formed [ 3 ].…”
Section: Discussionmentioning
confidence: 99%
“…6 Badiner et al reported that in 73% of uterine cornua analyzed after hysterectomy, tubal epithelial remnants were identified, with the median length of residual tubal epithelium of 6 mm. 7 Understanding the pathogenesis of HGSC is important for future prevention and management of the disease.…”
mentioning
confidence: 99%