Solitary fibrous tumor of the pancreas.

Autor: Baxter AR; Department of Surgery, New York University Langone Medical Center, New York, NY, USA., Newman E; Department of Surgery, New York University Langone Medical Center, New York, NY, USA elliot.newman@nyumc.org., Hajdu CH; Department of Pathology, New York University Langone Medical Center, New York, NY, USA.
Jazyk: angličtina
Zdroj: Journal of surgical case reports [J Surg Case Rep] 2015 Dec 01; Vol. 2015 (12). Date of Electronic Publication: 2015 Dec 01.
DOI: 10.1093/jscr/rjv144
Abstrakt: Solitary fibrous tumors (SFTs) are rare mesenchymal neoplasms of fibroblastic origin. Most commonly they affect the pleura but they been described in other viscera. SFT of the pancreas is extremely rare, and only eight cases have been reported to date. We perform a literature review and report a ninth case. The patient is a 54-year-old African-American female who presented with several months of abdominal pain. Abdominal radiography demonstrated a lesion in the head of the pancreas, and she underwent a Whipple operation. Pathology demonstrated SFT of the pancreas. She is alive and well 1 year post-operatively. SFT of the pancreas predominately affects middle-aged women. These tumors are difficult to distinguish radiologically from neuroendocrine tumors. While SFT of the pancreas tend to have an indolent course, there is the potential for malignancy. We recommend complete surgical excision.
(Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2015.)
Databáze: MEDLINE