Mathukumalli Neeharika L, Ali Niloufer, Kanikannan Meena A, Yareeda Sireesha
Department of Neurology, Nizam's Institute of Medical Sciences, Hyderabad, Telangana, India.
BMJ Case Rep. 2017 Oct 13;2017:bcr-2017-221874. doi: 10.1136/bcr-2017-221874.
We report an HIV patient aged 38 years with acute inflammatory demyelinating polyradiculoneuropathy subtype of Guillain-Barré syndrome (GBS) as the only manifestation of seroconversion and worsening of GBS being the harbinger of immune reconstitution inflammatory syndrome (IRIS). To date, only 5 cases of GBS during IRIS are reported. They manifested either during the third week or later after starting highly active antiretroviral therapy (HAART). Our patient witnessed worsening weakness by fifth day after starting HAART, even before the occurrence of pneumonia, cautioning one of the impending serious complications of IRIS and helped us initiate steroids at an early date.
我们报告了一名38岁的HIV患者,其患有吉兰-巴雷综合征(GBS)的急性炎症性脱髓鞘性多发性神经根神经病亚型,这是血清转化的唯一表现,而GBS的恶化是免疫重建炎症综合征(IRIS)的先兆。迄今为止,仅报告了5例IRIS期间发生GBS的病例。它们均在开始高效抗逆转录病毒治疗(HAART)后的第三周或更晚出现。我们的患者在开始HAART后的第五天出现了肌无力加重,甚至在肺炎发生之前,这警示了IRIS即将出现的严重并发症之一,并帮助我们尽早开始使用类固醇治疗。