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一名HIV感染患者中,格雷夫斯病和免疫性血小板减少性紫癜相继出现,作为免疫重建炎症综合征的表现。

Sequential occurrence of Graves' disease and immune thrombocytopenic purpura as manifestations of immune reconstitution inflammatory syndrome in an HIV-infected patient.

作者信息

Okazaki Masafumi, Nakamura Miho, Imai Akiko, Asagiri Tadashi, Takeuchi Seisho

机构信息

1 Department of Pharmacy, Kochi Medical School Hospital, Nankoku, Japan.

2 Department of General Medicine, Kochi Medical School Hospital, Nankoku, Japan.

出版信息

Int J STD AIDS. 2018 Jul;29(8):834-836. doi: 10.1177/0956462417752824. Epub 2018 Jan 23.

Abstract

Immune reconstitution inflammatory syndrome (IRIS) in HIV-infected patients after initiating antiretroviral therapy usually involves worsening manifestations of overt infectious disease. Here, we describe a sporadic case of a late-diagnosed HIV-positive man who developed Graves' disease as the first noninfectious IRIS followed by immune thrombocytopenic purpura as the second noninfectious IRIS.

摘要

在开始抗逆转录病毒治疗后,HIV感染患者出现的免疫重建炎症综合征(IRIS)通常表现为显性传染病症状的恶化。在此,我们描述了一例散发病例,一名晚期诊断的HIV阳性男性,首先出现格雷夫斯病作为首例非感染性IRIS,随后出现免疫性血小板减少性紫癜作为第二例非感染性IRIS。

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