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重症肌无力患者出现舌萎缩并伴有持续性构音障碍:10例患者报告

Atrophy of the tongue with persistent articulation disorder in myasthenia gravis: report of 10 patients.

作者信息

De Assis J L, Marchiori P E, Scaff M

机构信息

Department of Neurology, University of São Paulo Medical School, Brazil.

出版信息

Auris Nasus Larynx. 1994;21(4):215-8. doi: 10.1016/s0385-8146(12)80083-6.

Abstract

Ten patients with atrophy of the tongue, from a group of 752 with generalized acquired myasthenia gravis (MG), were studied. Tongue atrophy developed late in the majority of patients and was accompanied by tongue paresis (70% of the cases) and eventually associated to atrophy of other muscles of the palate, especially the uvula. All the patients exhibited severe forms of MG with bulbar involvement, mainly persistent dysphonia and dysphagia, almost always refractory to treatment. There is no correlation among atrophy of the tongue, sex, and thymus pathology. There is correlation between severeness of symptoms and early, persistent and treatment refractory dysphonia and dysphagia.

摘要

在一组752例全身性获得性重症肌无力(MG)患者中,对10例有舌萎缩的患者进行了研究。大多数患者的舌萎缩出现较晚,并伴有舌轻瘫(70%的病例),最终与腭部其他肌肉尤其是悬雍垂的萎缩相关。所有患者均表现为伴有延髓受累的重症MG,主要为持续性发音困难和吞咽困难,几乎总是对治疗无效。舌萎缩、性别和胸腺病理之间无相关性。症状的严重程度与早期、持续性和治疗难治性发音困难及吞咽困难之间存在相关性。

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