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[单中心异基因造血干细胞移植后肾病综合征的临床分析]

[The clinical analysis of nephrotic syndrome after allogeneic hematopoietic stem cell transplantation in one single center].

作者信息

Chen Yao, Huang Xiao-jun, Zhang Xiao-hui, Liu Dai-hong, Chen Huan, Han Wei, Wang Jing-zhi, Chen Yu-hong, Wang Yu, Wang Feng-rong, Zhao Ting, Liu Kai-yan, Xu Lan-ping

机构信息

Department of Hematology, Peking University People's Hospital, Beijing 100044, China.

出版信息

Zhonghua Nei Ke Za Zhi. 2011 Jul;50(7):572-5.

Abstract

OBJECTIVE

To explore the incidence, diagnosis and treatment of nephrotic syndrome (NS) following allogeneic hematopoietic stem cell transplantation (allo-HSCT) in one single center.

METHODS

Analysis were carried out based on the records of 1464 patients following allo-HSCT hospitalized in Peking University People's Hospital from January 1996 to April 2009, so as to evaluate the incidence and outcomes of NS. A total of 1464 patients whose survival time was longer than 100 d were enrolled. Eight patients (0.6%) had NS following allo-HSCT. Using the nested case-controlled study, 56 cases who received transplantation within the same period were selected as control group for risk factors analysis.

RESULTS

The median time of NS was 488 (54 - 1185) d after allo-HSCT. Lower extremities' edema and heavy proteinuria were present in all the patients. Two patients were accompanied with impaired renal function. Six patients suffered from chronic graft-versus-host disease (GVHD). Three patients with NS were accompanied with other symptoms of GVHD. Renal biopsy examination showed typical features of minimal change diseases in 3 patients and membranous nephropathy in 1 patient. All cases achieved complete remission (CR) after taking combined immunosuppressant agents. One patient relapsed soon after all the immunosuppressant agents were stopped. Six patients were still surviving with disease free. One patient died of the relapse of leukemia and another patient died of early discharge from hospital after allo-HSCT. The possible factors correlated with the occurrence of NS were analyzed, and the occurrence of chronic GVHD was identified as an independent factor of NS.

CONCLUSIONS

NS should be carefully taken into consideration when edema and proteinuria are present in patients following allo-HSCT. The occurrence of NS is probably related with chronic GVHD. NS responds well to immunosuppressant agents.

摘要

目的

探讨单中心异基因造血干细胞移植(allo-HSCT)后肾病综合征(NS)的发生率、诊断及治疗情况。

方法

基于1996年1月至2009年4月在北京大学人民医院住院的1464例allo-HSCT患者的记录进行分析,以评估NS的发生率及转归。共纳入1464例生存时间超过100天的患者。其中8例(0.6%)在allo-HSCT后发生NS。采用巢式病例对照研究,选取同期接受移植的56例患者作为对照组进行危险因素分析。

结果

NS发生的中位时间为allo-HSCT后488(54 - 1185)天。所有患者均出现下肢水肿及大量蛋白尿。2例患者伴有肾功能损害。6例患者发生慢性移植物抗宿主病(GVHD)。3例NS患者伴有GVHD的其他症状。肾活检检查显示3例患者为微小病变病的典型特征,1例为膜性肾病。所有病例在使用联合免疫抑制剂后均达到完全缓解(CR)。1例患者在停用所有免疫抑制剂后很快复发。6例患者仍无病存活。1例患者死于白血病复发,另1例患者死于allo-HSCT后过早出院。分析了与NS发生相关的可能因素,发现慢性GVHD的发生是NS的独立因素。

结论

allo-HSCT后的患者出现水肿和蛋白尿时应仔细考虑NS。NS的发生可能与慢性GVHD有关。NS对免疫抑制剂反应良好。

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