W. Mullges et al., IS CHRONIC DERMATOMYOSITIS OR POLYMYOSITI S WRONGLY DIAGNOSED AS ]]WEAKNESS IN THE ELDERLY]], Deutsche Medizinische Wochenschrift, 118(42), 1993, pp. 1520-1524
Two women, aged 72 (case 1) and 77 (case 2) were referred for neurolog
ical 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 classic
al dermatomyositis. Creatinine kinase concentration, never previously
measured, was 950 U/1. In case 2 there was polymyositis, previously no
t considered as she had a diabetic polyneuropathy and muscle enzyme co
ncentration was normal. In both cases the correct diagnosis was speedi
ly confirmed by electromyography and muscle biopsy. Immunosuppressive
treatment was largely successful in reversing the symptoms (case 1: in
itially 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 gl
ucocorticoid daily). - These two cases demonstrate that, particularly
in the elderly, dermatomyositis and polymyositis should be considered
in the differential diagnosis of progressive general weakness.