Case Report: Contiguous presentation of anti-MDA5 juvenile dermatomyositis and anti-AQP4 neuromyelitis optica spectrum disorder in an adolescent patient

Rebecca E. Wiersma, Zachary R. Shaheen, Colleen K. Correll, Patricia M. Hobday

Research output: Contribution to journalArticlepeer-review

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 languageEnglish (US)
Article number1376088
JournalFrontiers in Pediatrics
Volume12
DOIs
StatePublished - 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

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