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Nuclear matrix protein 2 antibody-positive adult dermatomyositis: a case report and review of the literature.

作者信息

Cartron Alexander M, Osler Montana, Chung Catherine, Trinidad John C

机构信息

Department of Dermatology, University of Maryland School of Medicine, Baltimore, MD.

出版信息

Dermatol Online J. 2020 Mar 20;26(3):13030/qt9n50x88m.

Abstract

Dermatomyositis is a clinically heterogenous inflammatory myopathy with unique cutaneous features. Myositis-specific antibodies can aid in diagnosis and anticipation of patient prognosis. Herein, we report a 22-year-old man who presented with multifocal erythematous plaques with violaceous papules on his bilateral elbows, neck, and face. He was diagnosed with biopsy-proven dermatomyositis and determined to be seropositive for nuclear matrix protein 2 antibody (NXP-2). He was treated with systemic corticosteroids, then intravenous methylprednisolone and azathioprine, and ultimately achieved greatest treatment response with intravenous immune globulin therapy.

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