Bartel C, Obermüller N, Rummel M J, Geiger H, Hauser I A
Department of Nephrology, University Hospital of Frankfurt/Main, Germany.
Clin Nephrol. 2008 Apr;69(4):285-9. doi: 10.5414/cnp69285.
In a 56-year-old white male patient, a membranoproliferative glomerulonephritis Type I was diagnosed after a 12-month history of low grade B cell lymphoma (Binet A). HIV, Hepatitis B and C serology were negative. Due to an impairment of renal function despite chemotherapy with COP, an immunochemotherapy consisting of rituximab (6 cycles) and bendamustine (4 cycles) was given. This therapeutic approach caused a complete remission of the nephrotic syndrome. Renal function and arterial hypertension improved markedly. In addition, urinary sediment became normal and proteinuria disappeared completely.
在一名56岁的白人男性患者中,在经历了12个月的低度B细胞淋巴瘤(Binet A期)病史后,被诊断为I型膜增生性肾小球肾炎。HIV、乙肝和丙肝血清学检查均为阴性。尽管采用COP方案化疗,但患者肾功能仍受损,遂给予由利妥昔单抗(6个周期)和苯达莫司汀(4个周期)组成的免疫化疗。这种治疗方法使肾病综合征完全缓解。肾功能和动脉高血压明显改善。此外,尿沉渣恢复正常,蛋白尿完全消失。