Early pulmonary manifestations of dermatomyositis : a case report

Introduction: Dermatomyositis (DM) is an idiopathic connective tissue disease with a wide range of systemic manifestations. Progressive proximal skeletal muscle weakness and symmetric and inflammatory infiltrates are the main clinical and histological features of DM. Case Presentation: In this study...

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Bibliographic Details
Published inIranian red crescent medical journal Vol. 22; no. 12; pp. 1 - 5
Main Authors Mozdourian, Mahnaz, Javidarabshahi, Zahra
Format Journal Article
LanguageEnglish
Published Dubai, United Arab Emirates Iranian Hospital 2020
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Summary:Introduction: Dermatomyositis (DM) is an idiopathic connective tissue disease with a wide range of systemic manifestations. Progressive proximal skeletal muscle weakness and symmetric and inflammatory infiltrates are the main clinical and histological features of DM. Case Presentation: In this study, we report the case of a 43-year-old male with DM and early pulmonary manifestations. A 50 mg/g daily dose of Prednisolone was administered for the case. The symptoms of muscle weakness improved after 2 weeks. Commonly, pulmonary diseases occur after the occurrence of other connective tissue diseases. However, in the present case, pulmonary manifestations were observed many years before the incidence of DM symptoms. Conclusion: The DM with Pulmonary involvement is associated with worse outcomes; accordingly, a higher rate of mortality is reported among these patients. Based on the literature, the neutrophil-lymphocyte ratio and platelet-lymphocyte ratio are reliable markers for the diagnosis of DM, along with lung problems.
ISSN:2074-1804
2074-1812
DOI:10.32592/ircmj.2020.22.12.48