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Treatment of early and refractory dermatomyositis with infliximab: a report of two cases

Identifieur interne : 001C37 ( Main/Exploration ); précédent : 001C36; suivant : 001C38

Treatment of early and refractory dermatomyositis with infliximab: a report of two cases

Auteurs : Sylvia Dold [États-Unis] ; Maria E. Justiniano [États-Unis] ; Javier Marquez [États-Unis] ; Luis R. Espinoza [États-Unis]

Source :

RBID : ISTEX:DAF806ABEE0884CEFCD89022798E8B37364B9E36

English descriptors

Abstract

Abstract: The idiopathic inflammatory myopathies embody the largest group of acquired and potentially treatable causes of skeletal muscle weakness. The three major groups of this disorder are polymyositis (PM), dermatomyositis (DM), and inclusion body myositis. Corticosteroids continue to be the mainstay of initial treatment in the majority of cases of PM/DM. The treatment of refractory disease can be challenging despite the utilization of the medications currently available. We report two patients with refractory DM who were treated with infliximab. We describe their presentation, clinical course, treatment, and outcomes.

Url:
DOI: 10.1007/s10067-006-0325-z


Affiliations:


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Le document en format XML

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