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肾移植受者背景为 BK 多瘤病毒肾病的膀胱 BK 多瘤病毒相关性尿路上皮癌。

BK Polyomavirus-Associated Urothelial Carcinoma of the Bladder with a Background of BK Polyomavirus Nephropathy in a Kidney Transplant Recipient.

机构信息

Department of Pathology, Sapporo City General Hospital, Sapporo, Japan.

Department of Pathology, National Institute of Infectious Disease, Tokyo, Japan.

出版信息

Nephron. 2023;147 Suppl 1:53-60. doi: 10.1159/000531822. Epub 2023 Aug 2.

Abstract

Renal transplant recipients are at increased risk for the development of a malignant neoplasm. Polyomavirus-associated urothelial carcinoma is a rare tumor that occurs in renal transplant recipients, with approximately 41 cases reported since 2002. It accounts for 27-31% of all post-transplant urothelial carcinomas and develops at an average of 8.5 years after transplantation. Histologically, it shows high-grade urothelial carcinoma (95.1%) with a high frequency of glandular differentiation and micropapillary structures (58.5%) and positive immunohistochemistry for polyomavirus large T antigen, p53 (92.9%), and p16 (100%). We encountered a case of BK polyomavirus (BKPyV)-associated urothelial carcinoma of the bladder diagnosed 54 months after kidney transplantation. Histologically, it was a high-grade urothelial carcinoma with micropapillary features, and immunohistochemically, it was diffusely positive for polyomavirus large T antigen, p16, and p53. BKPyV DNA and mRNA for BKPyV large T antigen have been identified in tissues using real-time polymerase chain reaction. The same sequence of the BKPyV VP1 genome hypervariable region was detected in both transplanted kidney tissue with polyomavirus nephropathy and urothelial carcinoma tissue, suggesting that polyomavirus-associated urothelial carcinoma developed in a background of persistent polyomavirus nephropathy. This case showed typical histological features and was detected and treated at an earlier stage than has been reported. It is important to keep in mind that polyomavirus-associated urothelial carcinoma can develop early after transplantation and might be associated with polyomavirus nephropathy. Because of its rapidly progressive nature, careful follow-up with urine cytology and cystoscopy is necessary. We report this case with a literature review.

摘要

肾移植受者发生恶性肿瘤的风险增加。多瘤病毒相关性尿路上皮癌是一种罕见的肿瘤,发生于肾移植受者,自 2002 年以来报告了约 41 例。它占所有移植后尿路上皮癌的 27-31%,并在移植后平均 8.5 年发展。组织学上,它表现为高级别尿路上皮癌(95.1%),具有较高的腺分化和微乳头状结构(58.5%),并且多瘤病毒大 T 抗原、p53(92.9%)和 p16(100%)的免疫组化阳性。我们遇到了一例肾移植后 54 个月诊断的 BK 多瘤病毒(BKPyV)相关性膀胱尿路上皮癌。组织学上,它是一种具有微乳头状特征的高级别尿路上皮癌,免疫组化染色显示多瘤病毒大 T 抗原、p16 和 p53 弥漫阳性。使用实时聚合酶链反应在组织中鉴定了 BKPyV 大 T 抗原的 BKPyV DNA 和 mRNA。在伴有多瘤病毒肾病和尿路上皮癌的移植肾组织中均检测到 BKPyV VP1 基因组高变区的相同序列,提示多瘤病毒相关性尿路上皮癌发生在持续多瘤病毒肾病的背景下。该病例具有典型的组织学特征,且比以往报道的更早被发现和治疗。重要的是要记住,多瘤病毒相关性尿路上皮癌在移植后早期即可发生,并且可能与多瘤病毒肾病有关。由于其快速进展的性质,需要密切随访尿细胞学和膀胱镜检查。我们报告了该病例并进行了文献复习。

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