首页> 美国卫生研究院文献>Iranian Journal of Pathology >Sarcomatoid Carcinoma of Renal Pelvis Involving Ureter and Renal Parenchyma with Heterologous Osteosarcomatous Differentiation: A Case Report and Review of Literature
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Sarcomatoid Carcinoma of Renal Pelvis Involving Ureter and Renal Parenchyma with Heterologous Osteosarcomatous Differentiation: A Case Report and Review of Literature

机译:肾盆腔肉瘤样癌累及输尿管和肾实质的异体骨肉瘤分化:一例病例并文献复习

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摘要

Sarcomatoid carcinoma is a highgrade rare malignant tumor with both epithelial and mesenchymal components. Sarcomatoid carcinoma in the upper urinary tract is very rare. We reported here a case of sarcomatoid carcinoma of renal pelvis with osteosarcomatous differentiation, with involvement of the ureter and renal parenchyma in a 68-year-old female. Histologically, predominant pleomorphic spindle cell sarcoma component with osteoid production and urothelial carcinoma component with in situ areas were identified. Immunohistochemical analysis showed vimentin positivity in sarcomatous component and cytokeratin positivity in carcinomatous component.
机译:肉瘤样癌是具有上皮和间质成分的高度罕见的恶性肿瘤。上尿路肉瘤样癌非常罕见。我们在这里报告了一名68岁女性的肾盂肉瘤样癌,伴有骨肉瘤分化,并伴有输尿管和肾实质。从组织学上,鉴定出具有类骨生成的主要多形性梭形细胞肉瘤成分和具有原位区域的尿路上皮癌成分。免疫组织化学分析显示肉瘤成分中波形蛋白阳性,癌性成分中细胞角蛋白阳性。

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