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一名呈现为严重混合性溶血性贫血的HIV患者发生免疫重建炎症综合征。

Immune reconstitution inflammatory syndrome in a patient with HIV presenting as severe mixed haemolytic anaemia.

作者信息

Mwirigi A, Stockwell S, Radia D, Kulasegaram R, Kesse-Adu R

机构信息

Guy's and St Thomas' NHS Foundation Trust, London, UK

Guy's and St Thomas' NHS Foundation Trust, London, UK.

出版信息

Int J STD AIDS. 2016 Oct;27(11):1019-22. doi: 10.1177/0956462415611521. Epub 2015 Oct 13.

Abstract

A patient with a delayed diagnosis of vertically transmitted HIV presented with a rare form of severe warm and cold (mixed) autoimmune haemolytic anaemia, six months after starting antiretroviral therapy. The CD4 count had responded rapidly to introduction of antiretroviral therapy, rising from 5 cells/µL to 93 cells/µL over the course of six months. The haemolysis was resistant to immunoglobulin therapy, eventually responding to corticosteroids. On careful scrutiny of the case, we found the features to be in keeping with immune reconstitution inflammatory syndrome; thorough investigations revealed no other trigger for haemolysis in this case.

摘要

一名垂直传播的HIV患者在开始抗逆转录病毒治疗6个月后,出现了一种罕见的严重温抗体型和冷抗体型(混合性)自身免疫性溶血性贫血,延迟诊断。抗逆转录病毒治疗开始后,CD4细胞计数迅速上升,在6个月内从5个/微升升至93个/微升。溶血对免疫球蛋白治疗耐药,最终对皮质类固醇有反应。经仔细检查该病例,我们发现这些特征符合免疫重建炎症综合征;全面调查显示,该病例中没有其他溶血诱因。

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