Resection and Abdominal Wall Reconstruction of a Desmoid Tumor with Endometrioma Features
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-...
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Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2016-01-01
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Series: | Case Reports in Surgery |
Online Access: | http://dx.doi.org/10.1155/2016/9453450 |
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Summary: | 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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ISSN: | 2090-6900 2090-6919 |