Hyperimmunoglobulin E syndrome with juvenile dermatomyositis and calcinosis
- نوع فایل : کتاب
- زبان : انگلیسی
- مؤلف : Bedangshu Saikia & Himanshu Aneja & Jyoti Jain & Jacob M. Puliyel
- چاپ و سال / کشور: 2010
Description
Juvenile dermatomyositis (JDM) is a rare childhood disease with autoimmune association. Environmental factors are known to trigger JDMin genetically susceptible individuals (Schmieder et al., Dermatol Online 6:3, 2009). Calcinosis is a well-established complication of JDM. Prevalence is higher in children (30–70%; ضzkaya et al., Erciyes Med J 30(1):40–43, 2008). Hyperimmunoglobulin E syndrome is a primary immunodeficiency syndrome with multiple recurrent abscess formation and raised serum immunoglobulin E levels. We report a case of JDM with calcinosis cutis universalis with hyperimmunoglobulin E syndrome. With a previous similar case report (Min et al., Korean J Intern Med 14:95–98, 1999), this could well be a new sequence syndrome where abscesses are the trigger for the onset of JDM
Clin Rheumatol Received: 12 February 2010 / Accepted: 15 March 2010
