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美法仑和泼尼松龙治疗原发性淀粉样变性的病例报告

Resolution of primary amyloidosis by melphalan and prednisolone: a case report.

作者信息

Nakayama M, Kashiwagi M, Katafuchi R, Hori K, Hayashi S, Fujimi S

机构信息

Department of Internal Medicine, Division of Nephrology and Clinical Research Institute, National Kyushu Medical Center Hospital, Fukuoka, Japan.

出版信息

Clin Nephrol. 2005 Mar;63(3):215-20. doi: 10.5414/cnp63215.

Abstract

We here report a case of a 50-year-old man who showed histologically evident resolution of primary amyloidosis by melphalan and prednisolone. The patient was admitted to our hospital for further evaluation of nephrotic syndrome and remarkable hepatomegaly with refractory ascites, on September 11, 1998. Laboratory tests at presentation showed nephrotic syndrome with slight renal impairment and elevation of the enzymes of the biliary system. Monoclonal light chains were not detected in the serum or urine by immunoelectrophoresis. A renal biopsy revealed global deposition of amyloid in all glomeruli, interstitium and blood vessels. Immunofluorescence staining was positive for kappa light chains. Liver biopsy specimens showed extensive deposition of amyloid along sinusoid walls. Bone marrow aspiration contained 7% plasma cells but no clusters or abnormal cells. Based on these findings, systemic AL- (amyloid light chain) amyloidosis was diagnosed, and the treatment with combinations of melphalan and prednisolone was started from October 1998 at intervals of 4-6 weeks. Renal impairment progressed, resulting in the initiation of maintenance hemodialysis in February 1999. Reinfusion of ascitic fluid into the hemodialysis circuit had been performed from March 1999 for refractory ascites, and ascites disappeared in July 1999. Furthermore, urinary output increased after 14 courses of chemotherapy. Renal function gradually ameliorated with a concomitant reduction in the enzymes of biliary system, and finally hemodialysis was discontinued in April 2001. Sixteen courses of chemotherapy were administered by April 2001. Proteinuria was negative in August 2001. A second renal biopsy was performed on November 20, 2001, which showed markedly decreased amyloid deposition and a proliferation of mesangial cells and increase in matrix in various degrees. We report a case of a patient with primary amyloidosis who was successfully treated by melphalan and prednisolone, resulting in marked resolution of renal amyloidosis.

摘要

我们在此报告一例50岁男性患者,其原发性淀粉样变性经美法仑和泼尼松龙治疗后组织学上有明显缓解。该患者于1998年9月11日因肾病综合征及伴有难治性腹水的显著肝肿大入院作进一步评估。入院时实验室检查显示为肾病综合征,伴有轻度肾功能损害及胆道系统酶升高。免疫电泳未在血清或尿液中检测到单克隆轻链。肾活检显示所有肾小球、间质和血管均有淀粉样物质弥漫性沉积。免疫荧光染色κ轻链呈阳性。肝活检标本显示沿肝血窦壁有广泛的淀粉样物质沉积。骨髓穿刺显示有7%的浆细胞,但无细胞簇或异常细胞。基于这些发现,诊断为系统性AL(淀粉样轻链)淀粉样变性,并于1998年10月开始每4 - 6周一次联合使用美法仑和泼尼松龙进行治疗。肾功能进行性恶化,于1999年2月开始维持性血液透析。自1999年3月起,因难治性腹水将腹水回输至血液透析回路,腹水于1999年7月消失。此外,化疗14个疗程后尿量增加。肾功能逐渐改善,同时胆道系统酶降低,最终于2001年4月停止血液透析。至2001年4月共进行了16个疗程的化疗。2001年8月蛋白尿转阴。2001年11月20日进行了第二次肾活检,结果显示淀粉样物质沉积明显减少,系膜细胞增生,基质不同程度增加。我们报告一例原发性淀粉样变性患者经美法仑和泼尼松龙成功治疗,肾淀粉样变性显著缓解的病例。

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