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重症肌无力伪装为急性脑卒中:病例报告。

Myasthenia gravis masquerading as acute stroke: a case report.

机构信息

Department of Neurology, Sree Narayana Institute of Medical Sciences (SNIMS), Kunnukara, India.

出版信息

Pan Afr Med J. 2020 Dec 2;37:305. doi: 10.11604/pamj.2020.37.305.27032. eCollection 2020.

Abstract

Among non-iatrogenic neuromuscular disorders, myasthenia gravis remains the most prevalent. Diagnosing this disorder may become challenging in certain cases such as in patients with coexisting comorbid illnesses and non-specific clinical symptoms. This is a case of atypical myasthenia gravis in a middle-aged hypertensive male, who initially presented symptoms suggestive of an acute ischemic stroke. Upon later investigation, prompted by persistent symptoms, the patient was found to have AchR antibodies and had the rare finding of a fissured and atrophied tongue (reversible on treatment). It is a well-known fact that brainstem strokes can present with bulbar weakness resulting in aspiration pneumonitis, as was with the clinical presentation in the below mentioned report. Due to the initial misdiagnosis, he had received medical therapy aimed towards stroke management and prevention. Further investigation leading to a definitive diagnosis, was followed by medical therapy with neostigmine, pyridostigmine and oral prednisolone, leading to significant improvement in symptoms. Hence as a mandatory measure, while dealing with a case of a new onset of weakness, especially in cranial musculature, myasthenia gravis must not be excluded from the list of differential diagnosis. Myasthenia gravis (MG) is a potential "stroke mimic" especially in the elderly. However, due to recent change in trends of stroke statistics, this disease should be considered a possibility even in younger patients.

摘要

在非医源性神经肌肉疾病中,重症肌无力仍然最为常见。在某些情况下,如同时患有合并症和非特异性临床症状的患者,诊断这种疾病可能具有挑战性。这是一位中年高血压男性的非典型重症肌无力病例,他最初表现出类似于急性缺血性中风的症状。在持续存在症状的情况下进一步检查后,发现患者存在乙酰胆碱受体抗体,并且舌裂和萎缩(治疗后可逆转)的罕见表现。众所周知,脑干中风可导致延髓无力,从而导致吸入性肺炎,如下所述的临床表现即为如此。由于最初的误诊,他接受了针对中风管理和预防的药物治疗。进一步的检查导致了明确的诊断,随后采用新斯的明、吡啶斯的明和口服泼尼松龙进行药物治疗,症状显著改善。因此,作为一项强制性措施,在处理新出现的无力,特别是颅部肌肉无力的病例时,绝不能将重症肌无力排除在鉴别诊断之外。重症肌无力(MG)是一种潜在的“中风模拟病”,尤其是在老年人中。然而,由于中风统计数据的趋势最近发生了变化,即使在年轻患者中,也应考虑这种疾病的可能性。

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