Resection and Abdominal Wall Reconstruction of a Desmoid Tumor with Endometrioma Features

Jaqueline Majors, Nathaniel F Stoikes, Nathaniel Stoikes, Reza Nejati, Jeremiah L. Deneve
Case reports in surgery · 2016 · vol. 2016 , pp. 1–4 · doi:10.1155/2016/9453450 · PMID:27247824 · W2373189987
article OA: gold CC0 ⤵ 2 in-corpus citations
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⚙ AI-generated summary by claude@2026-06, 2026-06-09 ⓘ

A 35-year-old female with a history of endometriosis underwent resection of an abdominal mass, which was pathologically confirmed as a desmoid tumor admixed with abdominal wall endometriosis.

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Abstract

Desmoid tumors are rare, musculoaponeurotic mesenchymal origin tumors arising from the proliferation of well-differentiated fibroblasts. Desmoid tumors may arise from any location with the abdominal cavity, abdominal wall and extremity locations being most frequent. We present the case of a 35-year-old female with a history of endometriosis who presented palpable abdominal mass and cyclic abdominal pain. Resection was performed for a presumed desmoid soft tissue tumor. Final pathology demonstrated desmoid histology admixed with abdominal wall endometriosis (endometrioma). This unique pathologic finding has only been rarely reported and is discussed with a brief review of the literature.

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endometriosisendometrioma

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

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