一个伴有全身性癫痫、可能的局灶性癫痫发作和功能性癫痫发作的复杂病例

IF 1.8 Q3 CLINICAL NEUROLOGY
Ahmed Elshetihy , Lema Nergiz , Thomas Cloppenborg , Friedrich G. Woermann , Birgitt Müffelmann , Christian G. Bien
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引用次数: 0

摘要

这名患者现年 42 岁,13 岁时出现遗传性全身癫痫(青少年肌阵挛性癫痫)。39 岁时,她经历了一次状态发作,在重症监护室接受了长时间的治疗。她留下了左侧海马硬化和可能的局灶性癫痫发作。此外,自 24 岁起,患者还在边缘型人格障碍的背景下出现功能性癫痫发作。虽然全身性癫痫发作可以通过抗癫痫药物(ASM)得到控制,但患者因功能性癫痫发作多次被送入急诊科,随后接受了包括插管在内的重症监护治疗。作为并发症,患者患上了重症多发性神经病和肌病,导致她不得不依赖轮椅。此外,在 ASM 外渗后,她还患上了复杂区域疼痛综合征。该报告表明,在全身强直-阵挛性癫痫状态发作后出现海马硬化的情况并不常见,而且与全身性和局灶性癫痫发作相比,功能性癫痫发作的治疗效果很差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A complex case with generalized epilepsy, probable focal seizures, and functional seizures

In this patient, now 42 years old, genetic generalized epilepsy (juvenile myoclonic epilepsy) manifested itself at the age of 13. At the age of 39, she experienced a status episode with prolonged ICU treatment. She was left with a left-sided hippocampal sclerosis and probably focal seizures. In addition, since the age of 24, the patient also experiences functional seizures on the background of a borderline personality disorder. While generalized epileptic seizures could be controlled with antiseizure medication (ASM), the patient was multiple times admitted to Emergency Departments for her functional seizures with subsequent intensive care treatments, including intubation. As a complication, the patient developed critical illness polyneuropathy and myopathy, resulting in wheelchair dependence. Additionally, she acquired a complex regional pain syndrome after extravasation of ASM. The report demonstrates the uncommon development of hippocampal sclerosis after a generalized tonic-clonic status epilepticus and the poor treatability of functional seizures as compared to generalized and focal seizures.

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来源期刊
Epilepsy and Behavior Reports
Epilepsy and Behavior Reports Medicine-Neurology (clinical)
CiteScore
2.70
自引率
13.30%
发文量
54
审稿时长
50 days
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