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[1例伴头部回缩样反射性肌阵挛及双侧下肢抽搐性肌阵挛的僵人综合征患者,经纵隔癌切除术后症状改善明显]

[A case of stiff-man syndrome with head retraction like reflex myoclonus and jerky myoclonus of bilateral lower extremities which responded well to removal of mediastinal carcinoma].

作者信息

Harada H, Hayashi A, Watanabe M, Tamaoka A, Shoji S

机构信息

Department of Neurology, University of Tsukuba.

出版信息

Rinsho Shinkeigaku. 1999 Oct;39(10):1025-8.

Abstract

A 58-year-old male presented with reflex myoclonus and stiffness of the left facial, tongue, shoulder, and lower limbs muscles. Muscle stiffness and gait progressively worsened, leading to frequent falls. Acoustic and cutaneous stimuli of head precipitated reflex myoclonus like head retraction. Cutaneous of lower extremities precipitated jerky myoclonus of bilateral lower extremities. CSF analysis were unremarkable. No anti GAD antibody or anti amphiphysin antibody was detected in the serum and CSF. On surface EMG the spasms initiated with 4-5 short burst discharges at intervals between 59 and 84 ms, followed by a tonic decrescendo activity up to 3 s. After diazepam treatment, stiffness and reflex myoclonus of lower extremities were disappeared and head retraction like reflex myoclonus was improved but remained. CT of the chest revealed a mediastinal tumor. Biopsy of the tumor revealed undifferential carcinoma. The patient further improved after the resection of the tumor. These findings suggest that this stiff-man syndrome may occur as an autoimmune paraneoplastic syndrome of CNS.

摘要

一名58岁男性出现反射性肌阵挛以及左侧面部、舌部、肩部和下肢肌肉僵硬。肌肉僵硬和步态逐渐恶化,导致频繁跌倒。头部的听觉和皮肤刺激会引发反射性肌阵挛,如头部回缩。下肢皮肤刺激会引发双侧下肢的抽搐性肌阵挛。脑脊液分析无异常。血清和脑脊液中未检测到抗谷氨酸脱羧酶抗体或抗 amphiphysin 抗体。在表面肌电图上,痉挛开始时伴有4 - 5次短阵发放,间隔时间在59至84毫秒之间,随后是长达3秒的强直性递减活动。地西泮治疗后,下肢的僵硬和反射性肌阵挛消失,头部回缩样反射性肌阵挛有所改善但仍存在。胸部CT显示纵隔肿瘤。肿瘤活检显示为未分化癌。肿瘤切除后患者进一步好转。这些发现表明,这种僵人综合征可能作为中枢神经系统的自身免疫性副肿瘤综合征出现。

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