Low-grade fibromyxoid sarcoma of the renal pelvis: first report.

Case reports in nephrology and urology Pub Date : 2012-07-01 Epub Date: 2012-07-10 DOI:10.1159/000341191
Aristeidis Alevizopoulos, Vasilis Mygdalis, Stayros Tyritzis, K Stravodimos, Constantinos A Constantinides
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引用次数: 16

Abstract

Sarcomas of the genitourinary tract are quite rare, accounting for 2.1% of all soft tissue sarcomas and have a poor prognosis. Kidney sarcomas are quite rare, representing 1–3% of malignant renal cases. Low-grade fibromyxoid sarcoma (LGFS) of the kidney is an exceedingly uncommon, indolent but metastasizing soft tissue sarcoma with deceptively benign-appearing histological features. The estimated 5-year overall survival seems to be over 90%, but very late local relapses and distant metastasis may occur, which underlines the need for a long-term follow-up. We present a case of a 48-year-old male patient with a LGFS located on the renal pelvis. This is probably the first report of LGFS arising from the renal pelvis.

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肾盂低度纤维黏液样肉瘤:首次报告。
发生在泌尿生殖系统的肉瘤十分罕见,约占所有软组织肉瘤的2.1%,预后较差。肾肉瘤相当罕见,约占恶性肾病例的1-3%。肾脏低级别纤维黏液样肉瘤(LGFS)是一种非常罕见的,惰性但转移的软组织肉瘤,具有看似良性的组织学特征。估计5年总生存率超过90%,但可能发生很晚的局部复发和远处转移,这强调了长期随访的必要性。我们报告一例48岁男性患者的LGFS位于肾盂。这可能是第一次报道起源于肾盂的LGFS。
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