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pubmed-article:8670340pubmed:abstractTextThis report describes a case of focal myositis in a patient with mixed connective tissue disease. The patient presented with diffuse neck swelling and pseudothrombophlebitis of the left internal jugular vein. Other clinical features included a high fever, elevated erythrocyte sedimentation rate, and prompt improvement after administration of high-dose intravenous corticosteroid therapy. Criteria for polymyositis were absent, serum levels of creatine kinase remained normal, and there was no sign of recurrence during 3 years of followup. Results of immunoprecipitation for anti-Jo-1 and other myositis-specific autoantibodies remained negative in serial serum samples obtained before, during, and after the episode.lld:pubmed
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pubmed-article:8670340pubmed:authorpubmed-author:LoveL ALAlld:pubmed
pubmed-article:8670340pubmed:authorpubmed-author:MillerF WFWlld:pubmed
pubmed-article:8670340pubmed:authorpubmed-author:SenécalJ LJLlld:pubmed
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pubmed-article:8670340pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:8670340pubmed:year1996lld:pubmed
pubmed-article:8670340pubmed:articleTitleFocal myositis presenting as pseudothrombophlebitis of the neck in a patient with mixed connective tissue disease.lld:pubmed
pubmed-article:8670340pubmed:affiliationHôpital Notre-Dame, University of Montreal Medical School, Québec, Canada.lld:pubmed
pubmed-article:8670340pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8670340pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:8670340pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed