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一名感染人类免疫缺陷病毒(HIV)儿童的眼阵挛-肌阵挛-共济失调综合征

Opsoclonus-myoclonus-ataxia syndrome in an HIV-infected child.

作者信息

Pereira Noella Maria Delia, Shah Ira, Kulkarni Shilpa

机构信息

Department of Pediatrics, Pediatric HIV Clinic , Bai Jerbai Wadia Hospital for Children , Dr Acharya Donde Marg , Parel , Mumbai , India.

Department of Pediatrics, Division of Pediatric Neurology , Bai Jerbai Wadia Hospital for Children , Dr Acharya Donde Marg, Parel, Mumbai, India.

出版信息

Oxf Med Case Reports. 2016 Oct 1;2016(10):omw077. doi: 10.1093/omcr/omw077. eCollection 2016 Oct.

Abstract

Opsoclonus-myoclonus-ataxia (OMA) syndrome typically presents with chaotic eye movements and myoclonus with some patients exhibiting ataxia and behavioural disturbances. The pathogenesis may be inflammatory with an infectious or paraneoplastic trigger. We present a 13-year-old HIV-infected girl who was initially started on highly active antiretroviral therapy (HAART) in March 2013 with a CD4 count of 79 cells/cumm. Initially, the patient did not comply with treatment, resulting in a CD4+ count of 77 cells/mm in November 2015 and prompting a new HAART scheme comprising lamivudine, tenofovir and ritonavir-boosted atazanavir. Shortly after starting this scheme, she developed OMA syndrome in January 2016. She was treated with intravenous immunoglobulin and methylprednisolone followed by oral steroids along with oral clonazepam and gradually recovered. We suggest immune reconstitution inflammatory syndrome as a possible aetiology of OMA in HIV-infected children.

摘要

眼阵挛-肌阵挛-共济失调(OMA)综合征通常表现为眼球运动紊乱和肌阵挛,部分患者还伴有共济失调和行为障碍。其发病机制可能是由感染或副肿瘤引发的炎症反应。我们报告一名13岁的感染HIV的女孩,她于2013年3月开始接受高效抗逆转录病毒治疗(HAART),当时CD4细胞计数为79个/立方毫米。起初,患者不依从治疗,导致2015年11月CD4+细胞计数降至77个/立方毫米,促使采用新的HAART方案,包括拉米夫定、替诺福韦和利托那韦增强的阿扎那韦。在开始该方案后不久,她于2016年1月患上OMA综合征。她接受了静脉注射免疫球蛋白和甲泼尼龙治疗,随后服用口服类固醇以及口服氯硝西泮,并逐渐康复。我们认为免疫重建炎症综合征可能是HIV感染儿童OMA的病因。

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