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首页> 外文期刊>South African medical journal = >Severe porphyric neuropathy - importance of screening for porphyria in Guillain-Barré syndrome
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Severe porphyric neuropathy - importance of screening for porphyria in Guillain-Barré syndrome

机译:严重的卟啉性神经病-格林-巴利综合征的卟啉症筛查的重要性

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The hepatic porphyrias are a group of rare metabolic disorders, each of which is associated with a specific enzymatic alteration in the haem biosynthesis pathway. In South Africa (SA), a high incidence of variegate porphyria (VP) is seen as a result of a founder effect, but acute intermittent porphyria (AIP) is also encountered. The development of acute neurovisceral attacks is related to environmental factors, including medications, hormones and diet. A possible manifestation of a severe attack is rapidly progressing quadriparesis, which may mimic Guillain- Barré syndrome. We present four such cases, highlighting that acute porphyria should be considered in the differential diagnosis of Guillain- Barré syndrome. Three patients presented to Steve Biko Academic Hospital, Pretoria, SA, with progressive quadriparesis, and one to a private hospital with acute abdominal pain followed by rapidly progressive quadriparesis. Two patients had started antiretroviral therapy before the development of symptoms, and one had started antituberculosis therapy. All patients had marked weakness with depressed reflexes, and showed varying degrees of confusion. An initial diagnosis of Guillain-Barré syndrome led to administration of intravenous immunoglobulins in two patients. On testing for porphyria, it was found that two patients had AIP and two VP. Electrophysiological investigations revealed severe mainly motor axonal neuropathy in all. Two patients deteriorated to the point of requiring mechanical ventilation, and one of them died due to complications of critical illness. Haemin was administered to three patients, but the process of obtaining this medication was slow, which delayed the recommended early administration. The surviving patients showed minimal recovery and remained severely disabled. Porphyric neuropathy should always be considered as a differential diagnosis in a patient with an acute neuropathy, especially in SA. Absence of abdominal pain does not exclude the possibility of porphyria, and attacks may be precipitated by antiretroviral and antituberculosis medication. The outcome of our patients was not favourable; specifically, obtaining haemin was a challenge in the state hospital setting.
机译:肝卟啉症是一组罕见的代谢紊乱,每一种都与血红素生物合成途径中的特定酶促改变有关。在南非(SA),由于建立者效应,杂色卟啉症(VP)的发生率很高,但是也遇到了急性间歇性卟啉症(AIP)。急性神经内脏发作的发展与环境因素有关,包括药物,激素和饮食。严重发作的可能表现是快速进行的四肢瘫痪,可能模仿吉兰-巴雷综合征。我们介绍了四个这样的案例,强调在Guillain-Barré综合征的鉴别诊断中应考虑急性卟啉症。三名患者因进行性四肢瘫痪而就诊于比勒陀利亚,比勒陀利亚的史蒂夫·比科学术医院,一例因急腹痛而急速进行性四肢瘫痪而进入私家医院。两名患者在出现症状之前就开始了抗逆转录病毒疗法,而一名患者已经开始了抗结核疗法。所有患者均表现为明显的无力,反射减弱,并表现出不同程度的意识模糊。吉兰-巴雷综合征的初步诊断导致两名患者静脉注射免疫球蛋白。在测试卟啉症时,发现两名患者患有AIP和两名VP。电生理学研究显示,严重的主要是运动轴索神经病。两名患者恶化到需要机械通气的程度,其中一名因严重疾病的并发症死亡。 Haemin被施用于三名患者,但是获得这种药物的过程很慢,这延迟了建议的早期给药。幸存的病人恢复得很少,并且仍然严重残疾。在患有急性神经病的患者中,特别是在SA中,应始终将卟啉性神经病视为鉴别诊断。没有腹痛并不能排除卟啉症,抗逆转录病毒和抗结核药物可能会引起发作。我们患者的结果并不理想。具体而言,在州立医院中获取血红蛋白是一项挑战。

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