ArticleCureus2025
Superimposed Segmental Juvenile Dermatomyositis: A Case Report.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Superimposed segmental juvenile dermatomyositis (SSJDM) is a rare and underrecognized variant of juvenile dermatomyositis (JDM) characterized by an initial, long-standing, well-defined lesion following Blaschko lines, later accompanied by classic cutaneous and systemic features. SSJDM likely results from early developmental genetic mutations causing loss of heterozygosity and type 2 cutaneous mosaicism. We describe an eight-year-old girl with morpheiform SSJDM and review the previously reported cases, analyzing clinical features, treatment, and outcomes. We also propose a clinical classification for the segmental presentations, which include morpheiform, linear calcinosis, lichenoid plaques, and erythematous-scaly plaques. This report aims to improve recognition of atypical segmental lesions to enable earlier diagnosis and treatment of JDM.
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Registered trials
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