Pelvic Fibromatosis Following Total Abdominal Hysterectomy with Bilateral Salpingo-oophorectomy: A Case Report

Desmoid tumours, also known as aggressive fibromatosis, are rare, benign, non-inflammatory, fibroblastic tumours. They are characterised by locally aggressive behaviour and a high potential for recurrence, but they do not metastasise. Here, the authors report the case of a 51-year-old female who presented with a lump in the lower abdomen for one month. The patient had a history of exploratory laparotomy with total abdominal hysterectomy and bilateral salpingo-oophorectomy for ovarian cystadenocarcinoma 15 years earlier. Following Ultrasonography (USG) and Contrast-Enhanced Computed Tomography (CECT) of the abdomen and pelvis, an exploratory laparotomy was performed, and a mass that was free from adjacent structures was excised. Histopathological examination revealed benign desmoid-type fibromatosis with osseous and chondroid metaplasia. The patient was discharged uneventfully. The current incidentally detected desmoid-type fibromatosis with osseous and chondroid metaplasia highlights the importance of vigilant follow-up and consideration of diverse pathologies, even in low-risk clinical scenarios.

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Publication Details

Journal
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
Published
2026-01-08
DOI
https://doi.org/10.7860/jcdr/2026/78943.22537
Primary Topic
Soft tissue tumor case studies
Type
article
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article

Pelvic Fibromatosis Following Total Abdominal Hysterectomy with Bilateral Salpingo-oophorectomy: A Case Report

Pratik Shaparia, Sagar Sarvaiya, Vaishakhi Shah
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
Soft tissue tumor case studies
article

Pelvic Fibromatosis Following Total Abdominal Hysterectomy with Bilateral Salpingo-oophorectomy: A Case Report

Pratik Shaparia, Sagar Sarvaiya, Vaishakhi Shah
article en

Abstract

Desmoid tumours, also known as aggressive fibromatosis, are rare, benign, non-inflammatory, fibroblastic tumours. They are characterised by locally aggressive behaviour and a high potential for recurrence, but they do not metastasise. Here, the authors report the case of a 51-year-old female who presented with a lump in the lower abdomen for one month. The patient had a history of exploratory laparotomy with total abdominal hysterectomy and bilateral salpingo-oophorectomy for ovarian cystadenocarcinoma 15 years earlier. Following Ultrasonography (USG) and Contrast-Enhanced Computed Tomography (CECT) of the abdomen and pelvis, an exploratory laparotomy was performed, and a mass that was free from adjacent structures was excised. Histopathological examination revealed benign desmoid-type fibromatosis with osseous and chondroid metaplasia. The patient was discharged uneventfully. The current incidentally detected desmoid-type fibromatosis with osseous and chondroid metaplasia highlights the importance of vigilant follow-up and consideration of diverse pathologies, even in low-risk clinical scenarios.

JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
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Soft tissue tumor case studies
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