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Juvenile dermatomyositis (JDM) is a rare condition, which causes inflammation in children’s skin and musculoskeletal systems. Symptoms include characteristic skin rashes on the face and extremities, muscle pain and weakness. This is a case report of a ten-year-old boy initially suspected of having lupus erythematosus. He was later diagnosed with JDM by
Vigand Svendsen, Sebastian +3 more
openaire +2 more sources
Calcinosis in juvenile dermatomyositis: Updates on pathogenesis and treatment
Calcinosis, or the deposition of insoluble calcium salts in the skin, subcutaneous tissue, fascia, tendons, and muscles, is a feared complication of juvenile dermatomyositis.
Caitlan S. Pinotti +4 more
doaj +1 more source
Distinct by Design: Unraveling the Unique Clinical and Transcriptomic Identity of Juvenile Scleromyositis Overlap Compared to Juvenile Systemic Sclerosis and Juvenile Dermatomyositis: Implications for Care and Pathogenesis. [PDF]
Objective To characterize clinical and transcriptomic differences in juvenile scleromyositis overlap (jOverlap) compared to juvenile systemic sclerosis (jSSc) and juvenile dermatomyositis (JDM), focusing on autoantibody profiles, organ involvement, treatment, and peripheral blood gene expression.
Robinson AD +6 more
europepmc +2 more sources
Transition From Juvenile Dermatomyositis to Spondyloarthritis: A Novel Overlapping Inflammatory Phenotype [PDF]
Objective Juvenile dermatomyositis (JDM) is a rare childhood inflammatory myopathy, whereas spondyloarthritis (SpA) is an inflammatory arthropathy characterized by enthesitis and peripheral or axial involvement. We describe a series of patients diagnosed with JDM in childhood who later fulfilled classification criteria for SpA, a sequential phenotype ...
Grooms A +3 more
europepmc +2 more sources
Background Juvenile dermatomyositis is an inflammatory disease of muscles, skin, and blood vessels of unknown cause affecting all age and ethnic groups, with a reported incidence of 1.9–4.1 per million.
Fatima Mussa +2 more
doaj +1 more source
Juvenile dermatomyositis and nephrotic syndrome: A case report and a mini literature review
BackgroundRenal involvement is rarely reported in juvenile dermatomyositis and may be caused by the toxic effects of myoglobinuria or an autoimmune reaction. We report a case of dermatomyositis and nephrotic syndrome in a child to explore the association
Weiran Zhou +4 more
doaj +1 more source
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
Sarah Hamdy Soliman +5 more
doaj +1 more source
Juvenile dermatomyositis is a rare autoimmune myopathy of childhood, associated with systemic vasculopathy, primarily affecting the capillaries. Panniculitis is seen histologically in about 10% of patients with dermatomyositis; however, its clinical ...
Dylan C Ginter +5 more
doaj +1 more source
Juvenile dermatomyositis (JDM) is a systemic capillary vasculopathy. Patients present with proximal muscle weakness, raised muscle enzymes, and pathognomic skin rashes such as heliotrope rash, Gottron's papules. Main complications are calcinosis, lipodystrophy, osteoporosis. Complement-mediated damage of vessels is a major mechanism. Magnetic resonance
openaire +3 more sources
Case of a fatal lung disease in a child with juvenile dermatomyositis
The article presents a case of a fatal lung disease in a child with juvenile dermatomyositis. Juvenile dermatomyositis is a serious disease with an unpredictable course, and lung damage in juvenile dermatomyositis is one of the most severe manifestations
O.A. Oshlianska +5 more
doaj +1 more source

