Large Uterine Angiolipoleiomyoma Masquerading as an Ovarian Tumor: A Case Report.

IF 0.6 Q4 SURGERY
Case Reports in Surgery Pub Date : 2026-09-12 eCollection Date: 2026-01-01 DOI:10.1155/cris/8616290
Prabineshwor Prasad Lekhak, Smriti Basnet, Hari Narayan Rai, Palistha Shakya, Tulsi Raj Khanal, Jyotsna Sharma Tiwari, Roshan Ghimire
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引用次数: 0

Abstract

Angiolipoleiomyoma (ALLM) is a rare benign mesenchymal tumor that primarily arises in the skin and kidney, and less frequently in the uterus. The present case may represent the largest reported uterine mass described as ALLM. We present a case of a 52-year-old woman with abdominal fullness and an irregular menstrual cycle having a large cystic abdominopelvic mass initially masquerading as a large ovarian tumor. Following successful tumor resection and subsequent histopathological and immunohistochemical analysis, a definitive diagnosis of uterine ALLM was established. This case shows that uterine ALLM can present with nonspecific clinical symptoms and radiologic features that mimic other pelvic pathologies, and should be considered in the differential diagnosis when evaluating pelvic masses in female patients.

伪装成卵巢肿瘤的大子宫血管脂质肌瘤1例。
血管脂质肌瘤(ALLM)是一种罕见的良性间质肿瘤,主要发生在皮肤和肾脏,很少发生在子宫。本病例可能是报道中最大的子宫肿块,称为ALLM。我们提出一个52岁的妇女腹部丰满和不规则的月经周期有一个大的囊性腹腔肿块最初伪装成一个大的卵巢肿瘤。在成功切除肿瘤和随后的组织病理学和免疫组织化学分析后,确定了子宫ALLM的明确诊断。本病例提示子宫ALLM可表现出非特异性临床症状和类似其他盆腔病变的影像学特征,在评估女性患者盆腔肿块时应考虑其鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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60
审稿时长
13 weeks
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