Abstract
Neuromyelitis optica spectrum disorder (NMOSD) is a rare inflammatory disorder of the central nervous system (CNS) that is known to be associated with other neurologic and organ-specific autoimmune conditions. There has been increasing recognition of the association between NMOSD and systemic autoimmune disease, most commonly systemic lupus erythematosus and Sjogren's syndrome. We report a case of an adolescent presenting with anti-melanoma differentiation-associated protein 5 juvenile dermatomyositis (anti-MDA5 JDM) and NMOSD, exhibiting clinical features of myelitis, polyarthritis, myositis, and skin involvement. Currently, only two other published cases have described NMOSD associated with anti-MDA5 dermatomyositis, both in adults. To the best of our knowledge, this is the first reported case in an adolescent patient.
Original language | English (US) |
---|---|
Article number | 1376088 |
Journal | Frontiers in Pediatrics |
Volume | 12 |
DOIs | |
State | Published - 2024 |
Bibliographical note
Publisher Copyright:2024 Wiersma, Shaheen, Correll and Hobday.
Keywords
- anti-aquaporin-4
- anti-melanoma differentiation-associated proteins 5
- case report
- dermatomyositis
- juvenile dermatomyositis
- neuromyelitis optica spectrum disorder
PubMed: MeSH publication types
- Case Reports
- Journal Article