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[蜱传播的神经系统慢性游走性红斑性脑膜多神经炎(加林-布雅杜,班瓦特病)]

[Meningopolyneuritis (Garin-Bujadoux, Bannwarth) erythema chronicum migrans disease of the nervous system transmitted by ticks].

作者信息

Schmidt R, Ackermann R

出版信息

Fortschr Neurol Psychiatr. 1985 May;53(5):145-53. doi: 10.1055/s-2007-1001962.

Abstract

The clinical spectrum of this remarkable non-syphilitic spirochaetosis (spirochaeta infection) of the nervous system is described in light of 53 further cases with reference to our earlier description of 47 cases. As the etiological diagnosis is not possible in all cases the knowledge of clinical courses is especially important. Males are affected almost twice as often as women. The disease is especially prevalent in the sixth decade. Usually, the syndrome begins in the warm season with exquisite pain and other sensory irritations in combination with marked malaise. Initial signs during the winter as well as painless clinical courses were also noted. About one half of the patients remembered contact with arthropodes or a chronic migrating erythema. In most cases (95%), asymmetrical peripheral signs followed the painful stage. More than two thirds of the patients showed affection of cranial nerves, usually facial palsy. Twenty percent demonstrated paresis of the extremities alone, the combination of involvement of cranial nerves and extremities was noted in one third of the cases. The sensory signs were usually only mild. Occasionally, the neurological impairment was limited to isolated sensory impairment. In contrast to the closely related Lyme disease, central nervous affection as well as cardiac and arthritic involvement is rare: 34 percent demonstrated mild psychopathological impairment; in one case a Babinski-phenomenon was elicited. Knee joint pain and gonarthritis were found in one case each. Even though meningeal signs were usually absent, the CSF showed alterations suggestive of chronic lymphocytic meningitis in all cases. At the same time, local synthesis of all three immune globulins was documented, especially of IgM (85%).

摘要

根据另外53例病例,并参考我们之前对47例病例的描述,阐述了这种显著的非梅毒螺旋体性神经系统螺旋体感染的临床谱。由于并非所有病例都能进行病因诊断,了解临床病程尤为重要。男性受影响的频率几乎是女性的两倍。该疾病在60岁左右尤为常见。通常,综合征在温暖季节开始,伴有剧痛和其他感觉刺激,并伴有明显的不适。也注意到冬季出现的初始症状以及无痛的临床病程。约一半的患者记得曾接触过节肢动物或出现过慢性游走性红斑。在大多数病例(95%)中,疼痛阶段后出现不对称的周围体征。超过三分之二的患者出现颅神经受累,通常为面神经麻痹。20%的患者仅表现为肢体轻瘫,三分之一的病例出现颅神经和肢体受累的组合。感觉体征通常较轻。偶尔,神经功能损害仅限于孤立的感觉障碍。与密切相关的莱姆病不同,中枢神经系统受累以及心脏和关节受累很少见:34%的患者表现出轻度精神病理损害;1例引出巴宾斯基征。各有1例出现膝关节疼痛和膝关节炎。尽管通常没有脑膜刺激征,但所有病例的脑脊液均显示出提示慢性淋巴细胞性脑膜炎的改变。同时,记录到所有三种免疫球蛋白的局部合成,尤其是IgM(85%)。

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