Abstract

Summary of Clinical Presentations and Relevant Investigation Findings in Previously Reported Cases of Kawasaki Disease With Myositis.TitleAuthor, Journal, Year Clinical PresentationRelevant Investigation Findings ConclusionMyositis in Kawasaki disease 8 Gama et al, Pediatr Neurol , 19908-Year-old boy, previously well, presented with clinical features of KD, diffused peripheral weakness, and respiratory failure•• CK: 1509 to 2657 IUMyositis is one of several neurological complications encountered in KD. The degree of CK elevation may be useful in predicting the severity of myopathy.•• EMG: myopathic pattern •• Muscle biopsy: atrophy and degenerationA case of polymyositis associated with Kawasaki disease 9 Sugie et al, Brain Dev , 19853-Year-old boy, previously well, was diagnosed with KD, and developed painful proximal muscle weakness in all extremities•• CK: 152 IU Polymyositis might be a complication of KD. Proximal muscle weakness suggests inflammatory myopathy, even if serum CK was not significantly elevated. •• EMG: myopathic change•• Muscle biopsy: mild architecture distortion, fiber atrophy, inflammatory cell infiltratesMyositis with Kawasaki’s disease

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