一名患有巴德-比德尔综合征的肾移植受者发生原发性中枢神经系统淋巴瘤。
Primary central nervous system lymphoma in a renal transplant recipient with Bardet-Biedl syndrome.
作者信息
Ersoy A, Kahvecioglu S, Bekar A, Aker S, Akdag I, Dilek K
机构信息
Department of Nephrology, Uludağ University Medical School, Bursa, Turkey.
出版信息
Transplant Proc. 2005 Dec;37(10):4323-5. doi: 10.1016/j.transproceed.2005.10.121.
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disorder. End-stage renal failure has been reported as the most frequent cause of death in this disorder. There are few reports of kidney transplantation in these patients. Renal transplant patients are known to be at increased risk for the development of malignancies. Although a few patients with BBS have been described to develop malignant disease, there was no previous association with lymphoma. We report a 20-year-old patient in whom primary central nervous system lymphoma was diagnosed 20 months after renal transplantation.
巴德-比德尔综合征（BBS）是一种罕见的常染色体隐性疾病。据报道，终末期肾衰竭是该疾病最常见的死亡原因。关于这些患者进行肾移植的报道很少。已知肾移植患者发生恶性肿瘤的风险增加。虽然已有少数BBS患者被描述发生恶性疾病，但此前尚无与淋巴瘤相关的报道。我们报告一名20岁患者，在肾移植20个月后被诊断为原发性中枢神经系统淋巴瘤。
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