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1. サルコイドミオパチーsarcoid myopathy [show details]
… diagnosis of sarcoid myopathy includes glucocorticoid- and other drug-induced myopathies, and, in patients with a muscle biopsy that reveals multiple noncaseating granulomas, other granulomatous diseases,… symptomatic myopathy have been described; these include a chronic myopathy, acute myositis, and nodular myopathy : Chronic myopathy – The most common form of sarcoid myopathy is the insidious…
2. 炎症性ミオパチーの病因pathogenesis of inflammatory myopathies [show details]
… Other forms of myositis have been described, some of which exhibit characteristic histologic features, including drug-induced myopathy, eosinophilic myositis, granulomatous myositis, and myositis associated …
3. 神経筋疾患の評価における筋酵素muscle enzymes in the evaluation of neuromuscular diseases [show details]
…number of conditions. These include: Inflammatory myopathies Infectious myopathies Dystrophinopathies Rhabdomyolysis Use of certain medications Metabolic myopathies Malignant hyperthermia …
4. 末梢神経疾患および筋疾患の鑑別診断differential diagnosis of peripheral nerve and muscle disease [show details]
…not a prominent symptom of myopathy. Most myopathic processes are relatively painless, including polymyositis, dermatomyositis, toxic myopathies, and inclusion body myositis. Generally, muscle pain is …
5. 封入体筋炎の臨床症状および診断clinical manifestations and diagnosis of inclusion body myositis [show details]
…differential diagnosis of IBM includes other idiopathic inflammatory myopathies (eg, dermatomyositis and polymyositis), hereditable inclusion body myopathies (hIBM), drug-induced myopathies, and amyotrophic lateral …

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Non-hereditary Myopathies

(1) Granulomatous myopathies including sarcoid myopathy Sarcoid myopathy or sarcoid myositis refers to sarcoidosis of the skeletal muscle, which presents with a histopathological presentation of non-caseating granulomas with giant cells in the muscle tissue.

Myopathies featuring non-caseating granulomas: Sarcoidosis ...

granulomatous myopathy of indeterminate cause) over a 21-year period. The median age at diagnosis was 67 years in sarcoid myopathy group, and 64 years in inclusion body myositis group. Three inclusion body myositis patients were initially diagnosed with sarcoid myopathy based on the presence of systemic

Myopathies featuring non-caseating granulomas: Sarcoidosis ...

Treatment outcomes are variable. We aimed to identify prognostic factors of treatment outcomes in myopathies featuring non-caseating granulomas. Sixteen patients were identified (9 sarcoid myopathy, 6 inclusion body myositis