A rare case report of a myxoid liposarcoma arising from the broad ligament.

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2022-01-01 DOI:10.1177/20363613221148839
Farah Sassi, Ghada Sahraoui, Lamia Charfi, Zemni Ines, Karima Mrad, Raoudha Doghri
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Abstract

Myxoid liposarcoma (MLPS) is the second most prevalent subtype of liposarcoma. It is usually found in the deep tissues of the lower limbs and rarely in gynecologic tract. Herein we present the second case in the English literature of a primary MLPS arising from the broad ligament which was thought to be a borderline ovarian tumor. The aim is to discuss its clinical and pathological characteristics. A 42-year-old woman presented with pelvic pain for the last 6 months. Magnetic resonance imaging was not specific. She underwent a surgical resection of the tumor mass, and pathological examination confirmed the diagnosis of MLPS deriving from the broad ligament. She received radiotherapy and the patient is doing well at 3 months follow-up. The clinical aspects, pathological diagnosis, prognosis, and therapy approach of broad ligament MLPS are all poorly understood. Complete surgical resection with or without radiotherapy is the mainstay of treatment in located MLPS.

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摘要一例发生于阔韧带的黏液样脂肪肉瘤。
黏液样脂肪肉瘤(MLPS)是第二常见的脂肪肉瘤亚型。它通常发生在下肢深部组织,很少发生在妇科。在这里,我们提出了第二个病例在英文文献中原发性MLPS起源于宽韧带,这被认为是一个边缘性卵巢肿瘤。目的是探讨其临床和病理特点。一名42岁女性,过去6个月出现骨盆疼痛。磁共振成像不明确。她接受手术切除肿瘤肿块,病理检查证实诊断为起源于阔韧带的MLPS。患者接受放射治疗,随访3个月,恢复良好。目前对宽韧带MLPS的临床、病理诊断、预后及治疗方法都知之甚少。完全手术切除加或不加放疗是定位性MLPS的主要治疗方法。
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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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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