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A case of multicentric Castleman's disease in HIV infection with the rare complication of acquired angioedema

机译:HIV感染多发性Castleman病一例,罕见后天性血管性水肿并发症

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摘要

Multicentric Castleman's disease (MCD), a polyclonal lymphoproliferative disorder of unknown aetiology, is a well-recognised complication of HIV disease. We present a case of MCD in an HIV-positive patient that is unusual on two counts: our patient's MCD first presented in the context of an immune restoration inflammatory syndrome ( IRIS), following the initiation of highly active antiretroviral therapy ( HAART). In addition, her MCD was associated with the unusual complication of acquired angioedema (AAE), which resolved following treatment of the MCD. While AAE is frequently found to have an underlying diagnosis of a lymphoproliferative disease, this is the first reported case linking AAE to MCD.
机译:多中心Castleman病(MCD)是一种病因不明的多克隆淋巴增生性疾病,是公认的HIV疾病并发症。我们介绍了一个HIV阳性患者的MCD病例,这在两个方面很不寻常:我们患者的MCD在高活性抗逆转录病毒疗法(HAART)启动后首先在免疫恢复性炎症综合症(IRIS)的背景下出现。此外,她的MCD与获得性血管水肿(AAE)的异常并发症有关,该并发症在MCD治疗后得以解决。虽然经常发现AAE具有淋巴增生性疾病的潜在诊断,但这是首次报道将AAE与MCD相关联的病例。

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