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[一名慢性酒精中毒患者的亚急性脑病伴癫痫发作(SESA综合征)]

[Subacute encephalopathy with epileptic seizures in a patient with chronic alcoholism (SESA syndrome)].

作者信息

Boroojerdi B, Hungs M, Biniek R, Noth J

机构信息

Neurologische Klinik, Universitätsklinikum der RWTH, Aachen.

出版信息

Nervenarzt. 1998 Feb;69(2):162-5. doi: 10.1007/s001150050254.

Abstract

Subacute encephalopathy with seizures in alcoholics (SESA syndrome) is a rare disease entity following chronic alcohol ingestion. It is quite distinct from alcohol withdrawal syndromes, such as delirium, withdrawal seizures or CNS complications of alcohol, such as Wernicke-Korsakow syndrome, central pontine myelinolysis or Marchiafava-Bignami disease, and was proposed in 1981 by Niedermeyer and coworkers. This syndrome consists of multiple neurological deficits, such as hemiparesis or hemianopia, and of recurrent focal and generalized seizures associated with prominent EEG features (periodic lateralized discharges, PLEDs). A 72-year-old Caucasian male with chronic alcoholism and an otherwise unremarkable past medical history was admitted to our hospital because of several secondary generalized simple partial seizures. Laboratory investigations revealed elevated levels of gamma-glutamyltranspeptidase and of mean corpuscular volume. Other laboratory investigations and the CSF examinations on three occasions revealed normal values. Cranial computed and magnetic resonance tomography showed cerebral microangiopathy and generalized atrophy. Despite triple anticonvulsive therapy and an intravenous treatment with acyclovir and thiamine, the epileptic seizures persisted. Several EEGs revealed left parietooccipital periodic lateralized epileptiform discharges (PLEDs). The patient died of an intercurrent pulmonary infection about 3 months after the onset of symptoms. The described clinical picture resembles the symptoms of SESA syndrome.

摘要

酒精性亚急性脑病伴癫痫发作(SESA综合征)是慢性饮酒后一种罕见的疾病实体。它与酒精戒断综合征(如谵妄、戒断性癫痫发作)或酒精性中枢神经系统并发症(如韦尼克-科尔萨科夫综合征、中央桥脑髓鞘溶解症或马奇亚法瓦-比尼亚米病)截然不同,由尼德迈耶及其同事于1981年提出。该综合征包括多种神经功能缺损,如偏瘫或偏盲,以及与突出的脑电图特征(周期性局灶性放电,PLEDs)相关的反复局灶性和全身性癫痫发作。一名72岁的白种男性,有慢性酒精中毒史,既往病史无其他异常,因数次继发性全身性单纯部分性癫痫发作入院。实验室检查显示γ-谷氨酰转肽酶水平和平均红细胞体积升高。其他实验室检查及三次脑脊液检查结果均正常。头颅计算机断层扫描和磁共振成像显示脑微血管病变和广泛性萎缩。尽管采用了三联抗惊厥治疗以及阿昔洛韦和硫胺素静脉治疗,癫痫发作仍持续存在。数次脑电图显示左顶枕部周期性局灶性癫痫样放电(PLEDs)。患者在症状出现后约3个月死于并发的肺部感染。所描述的临床表现类似于SESA综合征的症状。

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