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Primary antiphospholipid syndrome presenting as thrombotic microangiopathy: Successful treatment with steroids, plasma exchange and anticoagulants

机译:表现为血栓性微血管病的原发性抗磷脂综合征:成功使用类固醇,血浆置换和抗凝剂治疗

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摘要

Antiphospholipid syndrome (APS) often presents as a multisystem disorder characterized by recurrent arterial and venous thrombosis and pregnancy loss. We present a 46-year-old female who was admitted with oliguric acute renal failure. APS was suspected due to prolongation of activated partial thromboplastin time and history of miscarriages. Investigations for secondary causes were normal. Renal biopsy findings revealed thrombotic microangiopathy. A complete recovery of renal function was attained with a combination of plasma exchange and pulse methylprednisolone followed by oral steroids and warfarin. The case is presented for its rarity and therapeutic implications.
机译:抗磷脂综合征(APS)通常表现为多系统疾病,其特征是反复出现的动脉和静脉血栓形成和妊娠流失。我们介绍了一名46岁女性,其因少尿性急性肾衰竭而入院。怀疑由于活化的部分凝血活酶时间延长和流产史而导致APS。次要原因的调查很正常。肾脏活检发现血栓性微血管病。血浆置换和脉冲甲基强的松龙联合口服类固醇和华法林可以使肾功能完全恢复。该病例因其稀有性和治疗意义而被提出。

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