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肾移植后溶血性尿毒症综合征的复发

Recurrence of hemolytic uremic syndrome after renal transplantation.

作者信息

Seitz B, Albano L, Vocila F, Mzoughi S, Aoudia R, Guitard J, Ribes D, Vachet-Copponat H, Mourad G, Bienaimé F, Dahan P, Frémeaux-Bacchi V, Cassuto E

机构信息

Hôpital Pasteur, 30 Avenue de la Voie Romaine, 06002 Nice Cedex 1, France.

出版信息

Transplant Proc. 2007 Oct;39(8):2583-5. doi: 10.1016/j.transproceed.2007.08.021.

Abstract

Non-Shiga toxin-associated hemolytic uremic syndrome (non-Stx-HUS) is a rare disease. The clinical outcome is often unfavorable: 50% of patients progress to end-stage renal failure. Several mutations in complement regulatory genes predispose to non-Stx-HUS. Transplantation outcomes are poor among patients with either mutation in the genes encoding complement H or I factors, with 80% graft loss due to HUS recurrence. In contrast, patients with mutation in the gene encoding MCP have no disease relapse after transplantation. There are no treatment guidelines for non-Stx-HUS recurrence. Herein we have presented 8 patients with non-Stx-HUS recurrence after transplantation during the last 10 years in the South of France. HUS recurrence, which occurred early after transplantation in all but 1 patient, was treated by plasma exchange (PE) with substitution by fresh frozen plasma (FFP). Three patients still treated with long-term plasma therapy have no recurrence at 15, 19, or 24 months. An international registry would help to define new guidelines.

摘要

非志贺毒素相关性溶血尿毒综合征(non-Stx-HUS)是一种罕见疾病。临床预后通常不佳:50%的患者会进展为终末期肾衰竭。补体调节基因的几种突变易引发非Stx-HUS。在编码补体H因子或I因子的基因发生突变的患者中,移植结局较差,80%的移植物因HUS复发而丢失。相比之下,编码MCP的基因突变患者移植后无疾病复发。对于非Stx-HUS复发尚无治疗指南。在此,我们报告了法国南部过去10年中8例移植后发生非Stx-HUS复发的患者。除1例患者外,所有患者的HUS复发均发生在移植后早期,采用新鲜冷冻血浆(FFP)置换的血浆置换(PE)进行治疗。3例仍接受长期血浆治疗的患者在15、19或24个月时无复发。国际登记系统将有助于制定新的指南。

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