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一例最初表现为孤立性局灶性肌阵挛的脑型惠普尔病。

A case of cerebral Whipple's disease initially presenting with isolated focal myoclonus.

作者信息

Henning S, Tings T, Schmidt H, Tergau F, Wolf S, Scholz K, Knauth M, Buchner H, Gold R, Paulus W

机构信息

Department of Clinical Neurophysiology, Georg-August University, Göttingen, Germany.

出版信息

Eur J Neurol. 2006 Jun;13(6):659-61. doi: 10.1111/j.1468-1331.2006.01396.x.

Abstract

Neurological manifestations in Whipple's disease are highly variable and tend to occur at later stages of the disease. However, isolated, focal neurological symptoms are reported to be rare. Here we describe the successful treatment of a case of cerebral Whipple's disease initially presenting solely with isolated myoclonic jerks of the left hand and forearm evolving to a segmental myoclonus at a later stage. Additionally, we present - to our knowledge - a novel treatment by administration of immunomodulatory therapy (IVIg) in addition to established antibiotics.

摘要

惠普尔病的神经系统表现高度多变,且往往在疾病后期出现。然而,据报道孤立的局灶性神经系统症状较为罕见。在此,我们描述了一例脑型惠普尔病的成功治疗案例,该患者最初仅表现为左手和前臂的孤立性肌阵挛,后期发展为节段性肌阵挛。此外,据我们所知,除了使用已有的抗生素外,我们还采用了免疫调节疗法(静脉注射免疫球蛋白)进行了一种新的治疗方法。

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