临床荟萃 ›› 2022, Vol. 37 ›› Issue (7): 644-647.doi: 10.3969/j.issn.1004-583X.2022.07.012

• 论著 • 上一篇    下一篇

急性胰腺炎致Wernicke-Korsakoff综合征伴乳头体萎缩1例

郭卫娜1, 康宁2, 李晓莎2, 李玲2, 高俊淑2, 李娜2, 王天俊2()   

  1. 1.保定市第一中心医院 神经内科,河北 保定 071000
    2.河北省人民医院 神经内科,河北 石家庄 050000
  • 收稿日期:2020-10-19 出版日期:2022-07-20 发布日期:2022-08-30
  • 通讯作者: 王天俊 E-mail:wangtianj2007@126.com

One case report of Wernicke-Korsakoff syndrome with corpora candicans atrophy resulting from acute pancreatitis

Guo Weina1, Kang Ning2, Li Xiaosha2, Li Ling2, Gao Junshu2, Li Na2, Wang Tianjun2()   

  1. 1. Department of Neurology,Baoding No.1 Central Hospital,Baoding 071000,China
    2. Department of Neurology,Hebei General Hospital,Shijiazhuang 050000,China
  • Received:2020-10-19 Online:2022-07-20 Published:2022-08-30
  • Contact: Wang Tianjun E-mail:wangtianj2007@126.com

摘要:

目的 探讨Wernicke-Korsakoff综合征(WKS)的病因、临床表现、影像学特征及治疗方法。方法 回顾性分析1例急性胰腺炎致WKS伴乳头体萎缩病例,并复习相关文献。结果 患者女性,29岁,妊娠期间突发急性胰腺炎致剖宫产,经过长期禁食水、胃肠减压、血浆置换等治疗后逐渐出现Wernicke’s 脑病(Wernicke’s encephalopathy, WE)典型三联征表现,后期出现虚构、妄想及顺行性遗忘,头颅MR提示双侧丘脑近脑室对称性异常信号且乳头体逐渐萎缩,综上诊断为WKS,予以维生素B1治疗后恢复良好。结论 WKS是一种可治疗、可预防的疾病。对需较长时间禁食的患者,临床医生都应警惕该病的发生,注意补充维生素B1,避免造成不良后果。

关键词: 急性胰腺炎, 硫胺素, Wernicke-Korsakoff综合征, 乳头体萎缩

Abstract:

Objective To explore the etiology, clinical features, imaging characteristics and therapeutic regimen for Wernicke-Korsakoff syndrome(WKS). Methods One case of WKS associated with corpora candicans atrophy resulting from acute pancreatitis was retrospective analyzed, and related literature were reviewed. Results A 29-year-old female patient suffered from sudden acute pancreatitis during pregnancy, and was subject to cesarean section. Typical Wernicke's encephalopathy (WE) triad-sign manifestations were gradually found with the patient treated with long-term fasting & water deprivation, gastrointestinal decompressionand plasma exchange, the fabrication, delusion, anterograde forgetting and head nuclear magnetic were found with the patient later, symmetry abnormal signal of bilateral thalamus near ventricle and atrophic corpora candicans appeared gradual. The patient was comprehensively diagnosed as WKS and recovered well after vitamin B1 treatment. Conclusion WKS is a treatable and preventable disease. Clinicians should be alert to the occurrence of the disease for patients required to have fasting for a long time, and must supplement B1 to avoid adverse consequences.

Key words: acute pancreatitis, thiamine, Wernicke-Korsakoff syndrome, corpora candicans atrophy

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