{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T13:30:40Z","timestamp":1777901440397,"version":"3.51.4"},"reference-count":25,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[1986,1,1]],"date-time":"1986-01-01T00:00:00Z","timestamp":504921600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Scott Med J"],"published-print":{"date-parts":[[1986,1]]},"abstract":"<jats:p>Sixteen cases of dermatomyositis-polymyositis in children (dermatomyositis 15; polymyositis 1) have been reviewed. Proximal muscle weakness with a characteristic skin rash was vital for diagnosis in the majority of children. The positive laboratory tests such as creatine phosphokinase (CPK), electromyography (EMG) and muscle biopsy were helpful but results were normal in some cases even in the acute phase of the illness. All but one had been treated initially with high dose corticosteroids followed by a low dose maintenance for a prolonged period. Two in addition had had cytotoxic agents. Thirteen of the sixteen were currently in remission. In the other three cases, one with polymyositis only, the disease remained active and the two with dermatomyositis died. Only three of the patients were incapacitated by residual fixed contractures and extruding calcinosis. On the whole the prognosis of dermatomyositis is good.<\/jats:p>","DOI":"10.1177\/003693308603100104","type":"journal-article","created":{"date-parts":[[2017,1,10]],"date-time":"2017-01-10T15:31:51Z","timestamp":1484062311000},"page":"15-19","source":"Crossref","is-referenced-by-count":10,"title":["Dermatomyositis\u2014Polymyositis in Children"],"prefix":"10.1177","volume":"31","author":[{"given":"K. M.","family":"Goel","sequence":"first","affiliation":[{"name":"Rheumatology Clinic. Royal Hospital for Sick Children, Yorkhill, Glasgow"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"King","sequence":"additional","affiliation":[{"name":"Rheumatology Clinic. Royal Hospital for Sick Children, Yorkhill, Glasgow"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[1986,1,1]]},"reference":[{"key":"bibr1-003693308603100104","first-page":"407","volume-title":"Text book of paediatric rheumatology","author":"Sullivan DB","year":"1982"},{"key":"bibr2-003693308603100104","doi-asserted-by":"publisher","DOI":"10.1146\/annurev.me.17.020166.000431"},{"key":"bibr3-003693308603100104","first-page":"441","volume":"17","author":"Hanson V","year":"1967","journal-title":"Bull Rheum Dis"},{"key":"bibr4-003693308603100104","first-page":"202","volume-title":"Major problems in clinical paediatrics Vol XVI: Muscle disorders in childhood","author":"Dubowitz V","year":"1978"},{"key":"bibr5-003693308603100104","first-page":"177","volume-title":"Rheumatic disorders in childhood. 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Failure of disodium etidronate in calcinosis due to dermatomyositis and scleroderma. N Engl J Med 1974: 291\u2013296.","DOI":"10.1056\/NEJM197412122912408"},{"key":"bibr20-003693308603100104","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.1.5794.216"},{"key":"bibr21-003693308603100104","doi-asserted-by":"publisher","DOI":"10.1016\/S0307-742X(21)00486-0"},{"key":"bibr22-003693308603100104","doi-asserted-by":"publisher","DOI":"10.1016\/S0307-742X(21)00492-6"},{"key":"bibr23-003693308603100104","first-page":"511","volume":"26","author":"Berger RG","year":"1983","journal-title":"Arthritis and Rheumatism"},{"key":"bibr24-003693308603100104","first-page":"19","volume":"15","author":"Edwards RHT","year":"1981","journal-title":"J. Roy Coll Phys Lond"},{"key":"bibr25-003693308603100104","unstructured":"Lane RJM, Mosquera JE, Nicholson LVB,  Clinical, biochemical and histological responses to treatment in polymyositis. A prospective study (1982). 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