Erythroderma as a presenting sign of juvenile overlap syndrome

Juvenile dermatomyositis (JDM), which is rarely presented with erythroderma, and juvenile morphea are both autoimmune connective tissue diseases. We report a 14-year-old male child with resistant generalized erythroderma and mild proximal muscle weakness who was diagnosed with dermatomyositis. Later...

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Bibliographic Details
Main Authors: Sarah Hamdy Soliman (Author), Sameh Sarsik (Author), Nehal Mohamed Elshebiny (Author), Rania Ahmed El-Tatawy (Author), Noha Nabil Doghaim (Author), Nesrin Sabry Gomaa (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2023-01-01T00:00:00Z.
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Summary:Juvenile dermatomyositis (JDM), which is rarely presented with erythroderma, and juvenile morphea are both autoimmune connective tissue diseases. We report a 14-year-old male child with resistant generalized erythroderma and mild proximal muscle weakness who was diagnosed with dermatomyositis. Later, the patient developed morphea. The diagnosis of overlap syndrome was made by fulfilling Bohan and Peter's criteria for JDM as well as clinical manifestations of morphea.
Item Description:2319-7250
10.4103/ijpd.ijpd_45_23