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Clear Renal Cell Carcinoma with Angioleiomyomatous Stroma in a Noninherited Renal Cancer Syndrome: Is it a Different Entity?

机译:在非受阻肾癌症综合征中透明肾细胞癌,具有血管瘤性基质:它是不同的实体吗?

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摘要

Renal cell carcinoma (RCC) comprises only 3% of adult cancer cases. In most cases, patient is asymptomatic and the tumor mass is incidentally detected during radiological imaging for other medical conditions. Only one-third of patients with RCC present with hematuria, palpable tumor mass, or flank pain. Most of the cases of RCC are with clear or papillary cells, but a small subset of cases have demonstrated clear cell RCC with leiomyomatous stroma. The World Health Organization classification of tumors of the urinary system and male genital organs 2016 and the International Society Urological Pathology 2012 Vancouver classification have identified RCC with leiomyomatous stroma (RCCLMS) as an emerging entity of RCC. RCCLMS has been seen with inherited renal cancer syndromes such as tuberous sclerosis complex and von Hippel-Lindau disease. Here, we present a rare case of RCC with morphological and histopathological findings of the RCCLMS subset but showed noninherited mutational traits.
机译:肾细胞癌(RCC)仅占成人癌症病例的3%。在大多数情况下,患者无症状,在其他医疗条件下的放射成像中偶然发现肿瘤肿块。只有三分之一的RCC患者出现血尿、可触及的肿瘤肿块或腰痛。大多数RCC病例为透明细胞或乳头状细胞,但有一小部分病例为透明细胞RCC伴平滑肌瘤性基质。2016年世界卫生组织泌尿系统和男性生殖器官肿瘤分类和2012年国际泌尿病理学会温哥华分类已将伴有平滑肌瘤基质的肾细胞癌(RCCLMS)确定为肾细胞癌的一个新兴实体。RCCLMS可见于遗传性肾癌综合征,如结节性硬化综合征和von Hippel-Lindau病。在这里,我们提出了一例罕见的RCC病例,其RCCLMS亚群的形态学和组织病理学发现,但显示出非遗传性突变特征。

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