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首页> 外文期刊>Clinical Cancer Investigation Journal >Multilocular cystic renal cell carcinoma: A rare case report
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Multilocular cystic renal cell carcinoma: A rare case report

机译:多房囊性肾细胞癌:罕见病例报告

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Multilocular cystic renal cell carcinoma (MCRCC) is an uncommon low grade RCC with unique morphologic features. MCRCC also known as multilocular clear cell RCC is a rare cystic tumor of the kidney with an excellent outcome. MCRCC has been recognized as a separate subtype of RCC in the 2004 World Health Organization (WHO) classification of adult renal tumors. MCRCC is diagnosed on the basis of strict histological criteria according to 2004 WHO classification. It is usually included in the group of tumors of undetermined malignant potential with low nuclear grade. We present a case of MCRCC in a 43-year-old female patient who presented with pain in left lumbar region and hematuria. Left-sided radical nephrectomy was performed, and on histopathologic examination it was diagnosed as MCRCC with Fuhrman nuclear grade 1. Immunohistochemistry with epithelial membrane antigen and vimentin confirmed the diagnosis.
机译:多房囊性肾细胞癌(MCRCC)是一种罕见的低级RCC,具有独特的形态学特征。 MCRCC也称为多房透明细胞RCC,是一种罕见的肾脏囊性肿瘤,具有良好的预后。在2004年世界卫生组织(WHO)的成人肾肿瘤分类中,MCRCC被认为是RCC的一个独立亚型。根据2004年WHO分类标准,根据严格的组织学标准诊断MCRCC。它通常被包括在具有低核级的恶性潜能不确定的肿瘤组中。我们介绍了一名43岁女性患者的MCRCC病例,该患者出现左腰椎区域和血尿疼痛。进行了左侧根治性肾切除术,并在组织病理学检查中诊断为具有Fuhrman核级1的MCRCC。免疫组化与上皮膜抗原和波形蛋白一起证实了诊断。

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