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妊娠剧吐所致韦尼克脑病

Wernicke's encephalopathy induced by hyperemesis gravidarum.

作者信息

Gárdián G, Vörös E, Járdánházy T, Ungureán A, Vécsei L

机构信息

Department of Neurology, Albert Szent-Györgyi Medical University, Szeged, Hungary.

出版信息

Acta Neurol Scand. 1999 Mar;99(3):196-8. doi: 10.1111/j.1600-0404.1999.tb07344.x.

Abstract

A report is presented on a patient with Wernicke's encephalopathy secondary to hyperemesis gravidarum. The 25-year-old female presented 11 weeks into pregnancy with prolonged vomiting. Neurological examination 8 weeks later demonstrated obtunded sensations, nystagmus and ataxia of gait. MR imaging revealed bilateral lesions in the mediodorsal nuclei of thalami, in the hypothalamus and in the periaqueductal gray matter (1). The neurological signs and the MRI findings pointed to a diagnosis of Wernicke's encephalopathy. The patient was treated with intramuscular vitamin B1 followed by oral thiamine until the end of pregnancy. The subsequent course of the pregnancy was uncomplicated, and resulted in the delivery of a healthy 2970 g male infant. A review of the literature published during the last 30 years revealed an additional 20 cases of Wernicke's encephalopathy induced by hyperemesis gravidarum. Only half of these pregnancies resulted in the birth of a normal infant.

摘要

本文报告了一例因妊娠剧吐继发韦尼克脑病的患者。该25岁女性在怀孕11周时出现持续性呕吐。8周后进行神经系统检查,发现存在意识迟钝、眼球震颤和步态共济失调。磁共振成像显示双侧丘脑内侧背核、下丘脑和导水管周围灰质有病变(1)。神经系统体征和磁共振成像结果提示韦尼克脑病的诊断。患者先接受了肌肉注射维生素B1治疗,随后口服硫胺素直至妊娠结束。随后的妊娠过程顺利,产下一名健康的2970克男婴。回顾过去30年发表的文献,又发现了20例由妊娠剧吐诱发的韦尼克脑病病例。这些妊娠中只有一半产下正常婴儿。

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