它从何而来?骨盆-腹部巨大肿块,值得深思

Meera Kochuveetil Vijayakumar, Sheba Ann Zachariah, Jeswin Mathew
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引用次数: 0

摘要

输尿管细肌瘤是一种非常罕见的侵袭性腹膜后恶性肿瘤,术前准确诊断的可能性有限。输尿管细肌瘤的发病率极低。因此,文献中报道的病例很少。我们报告了一例 60 岁绝经后妇女的病例,患者出现腹胀和腹部不适。该病例最初被报告为左侧卵巢恶性肿瘤,因为病变明显向左侧附件区汇聚,且左侧卵巢未单独出现。此外,左肾有中度肾积水,左输尿管与病灶未分开。在输尿管狭窄和腹膜后肿瘤导致输尿管梗阻的病例中,应将雷米肉瘤作为鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Where does it come from? A large pelvi-abdominal mass with points to ponder
Ureteral leiomyosarcoma is a very rare aggressive retroperitoneal malignancy with limited possibility of an accurate pre-operative diagnosis. Incidence of ureter leiomyosarcoma is extremely rare. Hence, there is paucity of reported cases in the literature. We present a case of a 60-year-old postmenopausal woman presenting with abdominal distension and discomfort. This was initially reported as a malignancy arising from left ovary, as the lesion had apparent convergence toward left adnexal region and the left ovary was not seen separately. In addition, there was moderate hydronephrosis of the left kidney and left ureter was not separately made out from the lesion. Leiomyosarcoma should be considered as a differential diagnosis in cases of ureter stricture and retroperitoneal tumors causing ureteric obstruction.
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