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妊娠剧吐所致韦尼克脑病,计算机断层扫描和磁共振成像显示双侧尾状核病变。

Wernicke's encephalopathy induced by hyperemesis gravidarum, associated with bilateral caudate lesions on computed tomography and magnetic resonance imaging.

作者信息

Ohkoshi N, Ishii A, Shoji S

机构信息

Department of Neurology, University of Tsukuba, Japan.

出版信息

Eur Neurol. 1994;34(3):177-80. doi: 10.1159/000117034.

Abstract

The case of an 18-year-old woman with Wernicke's encephalopathy induced by hyperemesis gravidarum is reported. She had severe vomiting and received antiemetic therapy and intravenous administration of glucose and low-dose insulin solution without thiamine. She developed coma, nystagmus, ataxia and polyneuropathy. CT and MR imaging showed bilateral caudate lesions as well as symmetrical periventricular lesions of the thalamus and hypothalamus and periaqueductal gray matter. Caudate lesions are quite rare in Wernicke's encephalopathy.

摘要

报告了一例因妊娠剧吐诱发韦尼克脑病的18岁女性病例。她有严重呕吐症状,接受了止吐治疗,并静脉输注了葡萄糖和低剂量胰岛素溶液,但未补充硫胺素。她出现了昏迷、眼球震颤、共济失调和多发性神经病。CT和磁共振成像显示双侧尾状核病变以及丘脑、下丘脑和导水管周围灰质的对称性脑室周围病变。尾状核病变在韦尼克脑病中相当罕见。

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