| Literature DB >> 19723477 |
Astrid Schmieder1, Gregor von Komorowski, Wiebke K Peitsch, Sergij Goerdt, Matthias Goebeler.
Abstract
Juvenile dermatomyositis (JDM) is a rare autoimmune vasculopathy affecting children and adolescents under the age of 18. In this report we describe an 8-year-old boy who, besides myopathy, presented with an uncommonly broad spectrum of skin findings that had evolved after summer holidays at the Mediterranean Sea. Upon treatment with intravenous methylprednisolone the patient's condition considerably improved. Our case report illustrates that JDM requires comprehensive evaluation and multidisciplinary management.Entities:
Mesh:
Year: 2009 PMID: 19723477
Source DB: PubMed Journal: Dermatol Online J ISSN: 1087-2108