模拟原始肾细胞癌的肾静脉平滑肌肉瘤:一个不寻常的表现报告。

IF 0.7 Q4 PATHOLOGY Case Reports in Pathology Pub Date : 2021-05-12 eCollection Date: 2021-01-01 DOI:10.1155/2021/6637533
Amal Fekkar, Hafsa Elouazzani, Ahmed Jahid, Kaoutar Znati, Fouad Zouaidia, Zakia Bernoussi
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引用次数: 1

摘要

原发性血管源性平滑肌肉瘤(LMS)是一种罕见的肿瘤,超过一半的病例发生在下腔静脉(IVC)。原发性肾静脉LMS是一种极为罕见的肿瘤,文献报道的病例很少。他们的诊断仅依据病理特征。组织学上,它们由非典型纺锤形细胞组成,排列在长相交的束状结构中。肿瘤细胞在免疫组织化学中肌源性标志物染色呈阳性。标准治疗包括根治性肾切除术后化疗和/或放疗。由于组织学资料和随访不充分,预后因素尚未明确。肾静脉LMS总体预后较差。我们在此报告一例56岁男性患者发生的类似原始肾细胞癌的巨大右肾静脉LMS的例外病例。
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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Leiomyosarcoma of the Renal Vein Mimicking a Primitive Renal Cell Carcinoma: Case Report of an Unusual Presentation.

Primary leiomyosarcomas (LMS) of vascular origin are rare tumors, and more than half of the cases arise in the inferior vena cava (IVC). Primary LMS of the renal vein are extremely rare tumors with only a few cases reported in the literature. Their diagnosis is made only by pathological features. Histologically, they are made of atypical spindle-shaped cells arranged in long intersecting fascicles. Tumor cells stain positive for myogenic markers in immunohistochemistry. Standard treatment consists of radical nephrectomy followed by chemotherapy and/or radiotherapy. Because of insufficient histological data and follow-up, the prognosis factors are not well identified. Overall prognosis of renal vein LMS is poor. We report here an exceptional case of a huge LMS of the right renal vein mimicking a primitive renal cell carcinoma, occurring in a 56-year-old male patient.

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