Clear Cell Papillary Renal Cell Carcinoma: Case Series with Review of the Literature.

Anshima Singh, Ram Nawal Rao
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Abstract

Clear cell papillary renal cell carcinoma (CCPRCC) was included as a separate entity in the World Health Organisation classification of renal tumours in 2016. Immuno-histopathological and genetic characteristics are much known, but still, clinical features and long-term follow-up require more consolidated data. We report three cases of CCPRCC, detected in different clinical settings. The first case was co-incidentally diagnosed on routine imaging, in a follow-up case of open cystolithotripsy. The second case presented with haematuria under evaluation; and the third case presented with mild thrombocytopenia without anaemia or a positive Coombs test. All the cases revealed characteristic histopathological examination and immunohistochemistry. None of the patients showed tumour recurrence/metastases on follow-up. The study holds importance as it presents CCPRCC cases in different clinical scenarios, describes a rarely reported case of thrombocytopenia without associated anaemia/positive Coombs test, and emphasises the need to consider CCPRCC in relevant clinico-radiological settings and immuno-histopathological features, due to its indolent nature and consequently better prognosis.

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透明细胞乳头状肾细胞癌:病例系列及文献复习。
透明细胞乳头状肾细胞癌(CCPRCC)于2016年作为一个单独的实体被列入世界卫生组织肾肿瘤分类。免疫组织病理学和遗传特征是众所周知的,但仍然,临床特征和长期随访需要更多的巩固数据。我们报告三例CCPRCC,在不同的临床环境中检测到。第一个病例是在常规影像学上偶然诊断出来的,在一个随访的开放性膀胱碎石病例中。第二例出现血尿,正在评估中;第三例表现为轻度血小板减少症,无贫血或库姆斯试验阳性。所有病例均行特征性组织病理学检查和免疫组织化学检查。随访中,所有患者均未出现肿瘤复发/转移。该研究具有重要意义,因为它介绍了不同临床情况下的CCPRCC病例,描述了一例罕见的无相关贫血/ Coombs试验阳性的血小板减少病例,并强调需要在相关的临床放射学环境和免疫组织病理学特征中考虑CCPRCC,因为它的惰性性质,因此预后较好。
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