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Published on: August 19, 2021
Primary leiomyosarcoma of broad ligament
Fethi Ben Amara1, Hassen Jouini, Meher Nasr
1Department B of Obstetrics and Gynecology, CMNT, Tunisia.
La Tunisie Medicale
|December 11, 2007
Summary
This case report highlights a rare primary broad ligament leiomyosarcoma (LMS) in a 49-year-old woman. Early diagnosis and management of this unusual pelvic tumor remain challenging.
Area of Science:
- Gynecologic Oncology
- Surgical Pathology
- Rare Tumors
Background:
- Primary broad ligament leiomyosarcoma (LMS) is exceptionally rare, with limited documented cases.
- This report adds to the scarce literature on LMS in this anatomical location.
Observation:
- A 49-year-old woman presented with a right pelvic sidewall mass involving the appendix.
- Surgical intervention included hysterectomy, bilateral salpingo-oophorectomy, omentectomy, and appendicectomy.
Findings:
- The patient was diagnosed with leiomyosarcoma of the broad ligament with appendiceal involvement.
- Despite surgical intervention, the patient experienced a short-term survival, succumbing to the disease five months post-operatively.
Implications:
- This case underscores the diagnostic challenges associated with rare pelvic tumors like broad ligament LMS.
- Optimal management strategies for LMS in this unusual location require further investigation and case accumulation.