Cystic Lymphangiomyoma of the Uterus Mimicking an Ovarian Cyst: A Case Report

Authors

  • Dhouha Bacha Department of Pathology, Mongi Slim Hospital, Tunisia
  • Rania Battikh Department of Gynecology, Charles Nicolle Hospital, Tunisia
  • Dorsaf Beltaifa Department of Pathology, Sahloul Hospital, Sousse, Tunisia
  • Ahmed Halouani Department of Gynecology, Mongi Slim Hospital, Tunisia
  • Sana Ben Slama
  • Ahlem Lahmar Department of Pathology, Mongi Slim Hospital, Tunisia

DOI:

https://doi.org/10.71599/bhr.v6i1.174

Abstract

Background: Cystic lesions of the uterus are rare and are frequently misdiagnosed as adnexal pathology on imaging. Cystic lymphangiomyoma is an uncommon benign lesion characterized by dilated lymphatic channels within the uterine wall. Because imaging features are nonspecific, diagnosis generally requires histopathological confirmation supported by immunohistochemistry.

Case presentation: We report the case of a 34-year-old woman who presented with a pelvic cystic mass initially presumed to be of ovarian origin. Pelvic ultrasound and MRI suggested a paratubal cyst. Laparoscopy revealed a 6-cm intramural uterine cyst arising from the uterine wall. Laparoscopic cystectomy was performed with meticulous dissection to preserve the myometrium. Histopathological examination demonstrated multiple cystic spaces lined by flattened endothelial cells, consistent with uterine cystic lymphangiomyoma.

Conclusion: The postoperative course was uneventful. This rare case highlights the diagnostic challenge of distinguishing uterine cystic lesions from adnexal pathology based solely on imaging. Accurate diagnosis relies on histopathological and immunohistochemical evaluation, while complete surgical excision ensures definitive cure.

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Published

30-01-2026

How to Cite

Bacha , D., Battikh, R., Beltaifa , D., Halouani, A., Ben Slama , S., & Lahmar, A. (2026). Cystic Lymphangiomyoma of the Uterus Mimicking an Ovarian Cyst: A Case Report. Biomedicine & Healthcare Research, 6(1), 40–42. https://doi.org/10.71599/bhr.v6i1.174

Issue

Section

Case report

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