Uterine leiomyosarcoma in a postmenopausal woman: a case report

Authors

  • Samrat Kadam Department of Obstetrics and Gynecology, SKNMC and GH, Pune, Maharashtra, India
  • Shilpa Chaudhari Department of Obstetrics and Gynecology, SKNMC and GH, Pune, Maharashtra, India
  • Aparna Sasane Department of Obstetrics and Gynecology, SKNMC and GH, Pune, Maharashtra, India

DOI:

https://doi.org/10.18203/2320-1770.ijrcog20260577

Keywords:

Uterine leiomyosarcoma, Postmenopausal bleeding, Uterine sarcoma, Malignant smooth muscle tumor

Abstract

Uterine leiomyosarcoma (ULMS) is a rare but highly aggressive smooth muscle malignancy that often masquerades as benign fibroids, delaying diagnosis until advanced stages. The disease carries a grim prognosis, especially when clinical suspicion is low. We present the case of a 56-year-old multiparous, postmenopausal woman with a 20 day history of dysuria with unexpected vaginal bleeding. With no abdominal pain, postcoital bleeding, or systemic symptoms, the presentation initially appeared benign. However, imaging revealed a bulky uterus with mixed fibroid pathology and a thickened endometrium. Cytology was inconclusive for malignancy. Definitive diagnosis came from histopathological examination of endometrial curettage and a malignant fibroid polyp, revealing ULMS. Pelvic MRI confirmed lobulated anterior uterine wall lesions, pelvic lymphadenopathy, and endometrial collection. The patient underwent total abdominal hysterectomy with bilateral salpingo-oophorectomy and lymphadenectomy. This case highlights the silent yet aggressive nature of ULMS and the importance of a high index of suspicion, even in seemingly routine gynecological presentations. Timely surgical management remains the cornerstone of care in achieving disease control.

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Published

2026-02-25

How to Cite

Kadam, S., Chaudhari, S., & Sasane, A. (2026). Uterine leiomyosarcoma in a postmenopausal woman: a case report. International Journal of Reproduction, Contraception, Obstetrics and Gynecology, 15(3), 1096–1100. https://doi.org/10.18203/2320-1770.ijrcog20260577

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Section

Case Reports