A Rare Case of Juvenile Dermatomyositis (JDM)

Journal Title: Scholars Journal of Medical Case Reports - Year 2016, Vol 4, Issue 8

Abstract

JDM is a rare autoimmune vasculopathy affecting children and adolescents under the age of 18. A 5 year female child presented with myalgia, skin rash, abdominal pain and fever. On Observation Gottron papules, Heliotrope rash were present; EMG showed myopathic pattern. The Childs symptoms and clinical findings improved with corticosteroid and Methotrexate therapy. JDM is a rare vasculopathy, should be diagnosed and treated early to minimise disability and life-threatening complications. Keywords:vasculopathy, myopathy, skin rash.

Authors and Affiliations

Dipankar Mondal, Sreekanth R Shenoy, Shanti Sena Mishra, Simanta Das, Saroj Kumar Satapathy, Debasish Panigrahi

Keywords

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  • EP ID EP374000
  • DOI -
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How To Cite

Dipankar Mondal, Sreekanth R Shenoy, Shanti Sena Mishra, Simanta Das, Saroj Kumar Satapathy, Debasish Panigrahi (2016). A Rare Case of Juvenile Dermatomyositis (JDM). Scholars Journal of Medical Case Reports, 4(8), 607-609. https://europub.co.uk./articles/-A-374000