A rare case of leiomyosarcoma originating from the left round ligament of the uterus.

Q3 Pharmacology, Toxicology and Pharmaceutics Journal of Experimental Therapeutics and Oncology Pub Date : 2016-07-01
Metin Kaba, Aytekin Tokmak, Hakan Timur, Bülent Özdal, Levent Şirvan, Tayfun Güngör
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Abstract

Uterine leiomyosarcomas (LMS) are rare malignancies with a poor prognosis. The incidence is reported to be 3-7/100.000 per year. Preoperative and intraoperative differentiation between LMS and large leiomyoma is always challenging. Therefore, LMS are often diagnosed during postoperative histologic evaluation of hysterectomy or myomectomy specimens. LMS of the round ligament of the uterus which can represent as an inguinal or pelvic mass is extremely rare. To our knowledge, there is only one case report of LMS arising from the round ligament available in the literature. Herein, we aimed to present the second case of LMS originating from the left round ligament of the uterus in a premenopausal woman initially misdiagnosed as an ovarian tumor.

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一例罕见的起源于子宫左圆韧带的平滑肌肉瘤。
子宫平滑肌肉瘤是一种少见的恶性肿瘤,预后较差。据报道,每年的发病率为3-7/10万。LMS和大平滑肌瘤的术前和术中鉴别一直是一个挑战。因此,LMS通常在子宫切除术或子宫肌瘤切除术标本的术后组织学评估中被诊断出来。子宫圆韧带的LMS可以表现为腹股沟或盆腔肿块是非常罕见的。据我们所知,文献中只有一例由圆形韧带引起的LMS报告。在此,我们的目的是提出第二例LMS起源于子宫左圆韧带的绝经前妇女最初误诊为卵巢肿瘤。
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