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肾移植术后早期发生的与他克莫司相关的局限性血栓性微血管病。

Tacrolimus associated localized thrombotic microangiopathy developing in early stage after renal transplantation.

作者信息

Devadoss Clement Wilfred, Vijaya V Mysorekar, E Mahesh, Venkataramana S Raju, M S Girish

机构信息

Assistant Professor, Department of Pathology, M.S. Ramaiah Medical College , Bangalore, India.

出版信息

J Clin Diagn Res. 2012 Dec;6(10):1786-8. doi: 10.7860/JCDR/2012/4535.2614. Epub 2012 Dec 15.

Abstract

Calcineurin inhibitor induced thrombotic microangiopathy is a rare but well recognized complication of a renal transplantation that occurs in 1% of the patients who are on tacrolimus immunosuppression. Among the other aetiological factors of the "de-novo" Thrombotic Microangiopathy (TMA), the condition especially has to be differentiated from an antibody mediated rejection, as both have different pathogenesis, therapeutic connotations and outcomes.We report a case of a middle aged female renal transplant recipient treated with tacrolimus, who developed localised thrombotic microangiopathy in the early post transplantation period. Despite the normal trough levels of tacrolimus, a diagnosis of "Tacrolimus induced TMA" was rendered after excluding other causes of the "de-novo" TMA, which included an antibody mediated rejection, a meticulous clinico-pathological correlation and serological studies. The treatment included the substitution of tacrolimus by rapamycin, with the subsequent normalization of the renal function.

摘要

钙调神经磷酸酶抑制剂诱导的血栓性微血管病是肾移植中一种罕见但已得到充分认识的并发症,发生在接受他克莫司免疫抑制治疗的患者中的比例为1%。在“新发”血栓性微血管病(TMA)的其他病因中,这种情况尤其需要与抗体介导的排斥反应相鉴别,因为两者具有不同的发病机制、治疗内涵和结局。我们报告一例中年女性肾移植受者,接受他克莫司治疗,在移植后早期发生局限性血栓性微血管病。尽管他克莫司谷值水平正常,但在排除“新发”TMA的其他原因(包括抗体介导的排斥反应)后,通过细致的临床病理相关性分析和血清学研究,诊断为“他克莫司诱导的TMA”。治疗措施包括用雷帕霉素替代他克莫司,随后肾功能恢复正常。

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