原发性肾多形性未分化肉瘤:病例报告和文献综述

IF 0.1 Q4 ONCOLOGY
Milagros Abad-Licham , Daniel Carbajal-Vásquez , Patricia Coral-González , Teresa Cusma-Quintana , Eloy Silva-Capuñay , Juan Astigueta-Pérez
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引用次数: 0

摘要

原发性肾脏肉瘤是一种罕见的肿瘤,约占恶性肿瘤的1-3%。最常见的组织学类型是平滑肌肉瘤和脂肪肉瘤。原发性肾脏多形性未分化肉瘤是一种罕见的变异,预后较差,目前文献报道约60例。我们报告一位52岁的女性高肾肿瘤患者,经手术治疗,其免疫组织化学组织学诊断为未分化多形性肉瘤,巨细胞变异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sarcoma indiferenciado pleomórfico primario renal: reporte de caso y revisión de la literatura

Primary sarcomas of the kidney are a rare entity and it counts for 1-3% of malignant neoplasms. The most frequent histologic types are leiomyosarcoma and liposarcoma. The primary pleomorphic undifferentiated sarcoma of kidney is a rare variant and it has a poor prognosis, with around 60 cases described in the literature up to date. We present a 52-year-old female case with high renal tumor, treated surgically whose histological diagnosis confirmed by immunohistochemistry was undifferentiated pleomorphic sarcoma, giant cell variant.

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