Kuppachi S, Holanda D, Eberlein M, Alexiev B, Tyler A J, Wissel M C, Kleiboeker S B, Thomas C P
Division of Nephrology, Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA.
Department of Pathology, University of Iowa Carver College of Medicine, Iowa City, IA.
Am J Transplant. 2017 Mar;17(3):813-818. doi: 10.1111/ajt.14057. Epub 2016 Oct 21.
We report a lung transplant recipient who developed BK polyoma virus (BKPyV) DNAemia and BKPyV nephropathy. With careful management of his immunosuppression he achieved significant reduction in BKPyV DNAemia and stabilization of his kidney function. He later developed a high-grade bladder cancer and shortly thereafter he experienced a major upsurge in the level of BKPyV DNAemia that coincided with the discovery of hepatic metastasis. Retrospectively, the bladder cancer and the hepatic secondary tumor stained uniformly for SV40 large T antigen, and the BKPyV DNA sequences identified in plasma corresponded to BKPyV DNA within hepatic tissue, indicating that the spike in BKPyV load was likely derived from the circulating tumor cells or cell-free tumor DNA following metastases of a BKV-associated cancer. To the best of our knowledge, this is the first description of a surge in BKPyV load in a patient with controlled BKPyVN that heralded the appearance of a metastatic urothelial malignancy. This report discusses the literature on BKPyV-associated malignancies and the possibility that unexplained increases in BKPyV DNAemia may be a biomarker for metastatic BKPyV-related urothelial cancer.
我们报告了一名肺移植受者,其发生了BK多瘤病毒(BKPyV)血症和BKPyV肾病。通过对其免疫抑制进行谨慎管理,他的BKPyV血症得到显著降低,肾功能得以稳定。他后来患上了高级别膀胱癌,此后不久,他的BKPyV血症水平大幅上升,这与肝转移的发现同时发生。回顾性分析发现,膀胱癌和肝转移瘤均一致表达SV40大T抗原,血浆中鉴定出的BKPyV DNA序列与肝组织中的BKPyV DNA相对应,这表明BKPyV载量的激增可能源自与BKV相关癌症转移后的循环肿瘤细胞或游离肿瘤DNA。据我们所知,这是首次描述在BKPyV肾病得到控制的患者中BKPyV载量激增预示着转移性尿路上皮恶性肿瘤的出现。本报告讨论了关于BKPyV相关恶性肿瘤的文献,以及BKPyV血症无法解释的升高可能是转移性BKPyV相关尿路上皮癌生物标志物的可能性。