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[眼肌型重症肌无力:临床病程及治疗策略]

[Ocular myasthenia: clinical course and strategies for treatment].

作者信息

Marzo M E, Pérez López-Fraile I, Capablo J L, Ara J R, Usón M

机构信息

Servicio de Neurología, Hospital Miguel Servet, Zaragoza, España.

出版信息

Rev Neurol. 1998 Mar;26(151):398-400.

PMID:9585951
Abstract

INTRODUCTION

Ocular myasthenia gravis is a localized form of myasthenia in which only the extra-ocular muscles are clinically affected, namely the levator palpebrae superioris and orbicularis oculi. Two years after onset of the ocular condition, it became generalized in 44-53% of the patients.

OBJECTIVE

  1. To describe the clinical features, diagnostic characteristics and clinical course of seven patients who fulfilled the criteria for diagnosis of ocular myasthenia and in whom the condition did not become generalized: 2. Review recent papers on this. Material and methods. We studied seven patients (two men and two women) diagnosed as having ocular myasthenia gravis, and followed them up for at least three years.

RESULTS

The average age was 56.5. The clinical findings were of ptosis of the eyelids and diplopia. All seven patients were treated with pyridostigmine. In six cases prednisone was also given and in one patient thymectomy was done. There was a satisfactory result in all cases.

CONCLUSIONS

The basic treatment of ocular myasthenia is with anticholinesterases and corticosteroids. Occasionally other immunosuppressives may be required. Prednisone seems to reduce the number of patients who go on to develop the generalized form.

摘要

引言

眼肌型重症肌无力是重症肌无力的一种局部形式,临床上仅眼外肌受累,即上睑提肌和眼轮匝肌。眼部疾病发病两年后,44% - 53%的患者病情会发展为全身型。

目的

  1. 描述7例符合眼肌型重症肌无力诊断标准且病情未发展为全身型患者的临床特征、诊断特点及临床病程。2. 回顾近期关于此方面的文献。材料与方法。我们研究了7例被诊断为眼肌型重症肌无力的患者(2男5女),并对他们进行了至少三年的随访。

结果

平均年龄为56.5岁。临床症状为眼睑下垂和复视。所有7例患者均接受了吡啶斯的明治疗。6例患者还使用了泼尼松,1例患者接受了胸腺切除术。所有病例均取得了满意的效果。

结论

眼肌型重症肌无力的基本治疗方法是使用抗胆碱酯酶药物和皮质类固醇。偶尔可能需要其他免疫抑制剂。泼尼松似乎能减少发展为全身型的患者数量。

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