Ampullary adenocarcinoma in neurofibromatosis type 1. Case report and literature review

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Abstract

Periampullary tumors in patients affected by Neurofibromatosis Type 1 (NF-1) are usually carcinoids or stromal tumors and, rarely, adenocarcinomas. We report a case of an adenocarcinoma of the ampulla of Vater in a 54-year-old woman with NF-1 admitted to the hospital with jaundice and undergoing pancreato-duodenectomy. Histologically, the resected specimen showed an adenocarcinoma of the ampulla as being a part of a complex atypical epithelial proliferation extended from the papilla to the mucosa of the duodenum and distal choledochus, islet-cell adenomatosis of the pancreas and multiple gastric, duodenal, jejunal stromal tumors. The ampullary and periampullary adenocarcinomas in NF-1 patients have peculiar features, suggesting a widespread predisposition to cancer development in periampullary tissues and requiring widely demolitive surgery. Moreover, they occur at a younger age than those occurring in non-NF-1 patients, may be associated with additional periampullary epithelial tumors, are often operable and may present long survival.

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CITATION STYLE

APA

Costi, R., Caruana, P., Sarli, L., Violi, V., Roncoroni, L., & Bordi, C. (2001). Ampullary adenocarcinoma in neurofibromatosis type 1. Case report and literature review. Modern Pathology, 14(11), 1169–1174. https://doi.org/10.1038/modpathol.3880454

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