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[慢性皮肤炎或多发性肌炎是否被误诊为“老年虚弱症”?]

[Is chronic dermato- or polymyositis misdiagnosed as "weakness of old age"?].

作者信息

Müllges W, Naumann M, Reichmann H

机构信息

Neurologische Klinik, Universität Würzburg.

出版信息

Dtsch Med Wochenschr. 1993 Oct 22;118(42):1520-4. doi: 10.1055/s-2008-1059480.

Abstract

Two women, aged 72 (case 1) and 77 (case 2) were referred for neurological diagnosis because of progressive muscular weakness, for 4 and 18 months, respectively, which had finally led to dysphagia and required mechanical ventilation. The cause of the disease in case 1 was classical dermatomyositis. Creatinine kinase concentration, never previously measured, was 950 U/l. In case 2 there was polymyositis, previously not considered as she had a diabetic polyneuropathy and muscle enzyme concentration was normal. In both cases the correct diagnosis was speedily confirmed by electromyography and muscle biopsy. Immunosuppressive treatment was largely successful in reversing the symptoms (case 1: initially 500 mg methylprednisolone daily, reduced to 50 mg daily within 6 weeks; case 2: 500 mg methylprednisolone daily for 1 week, then 100 mg daily plus 150 mg azathioprine with maintenance dosage of 20 mg glucocorticoid daily).--These two cases demonstrate that, particularly in the elderly, dermatomyositis and polymyositis should be considered in the differential diagnosis of progressive general weakness.

摘要

两名女性,年龄分别为72岁(病例1)和77岁(病例2),因进行性肌肉无力分别被转诊进行神经学诊断,病程分别为4个月和18个月,最终导致吞咽困难并需要机械通气。病例1的病因是典型的皮肌炎。此前从未检测过的肌酸激酶浓度为950 U/l。病例2为多发性肌炎,由于她患有糖尿病性多发性神经病且肌肉酶浓度正常,此前未被考虑到。在这两个病例中,通过肌电图和肌肉活检迅速确诊。免疫抑制治疗在很大程度上成功逆转了症状(病例1:最初每日500 mg甲泼尼龙,6周内减至每日50 mg;病例2:每日500 mg甲泼尼龙治疗1周,然后每日100 mg加150 mg硫唑嘌呤,糖皮质激素维持剂量为每日20 mg)。——这两个病例表明,特别是在老年人中,进行性全身无力的鉴别诊断应考虑皮肌炎和多发性肌炎。

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