Neuropsychiatric manifestations in an adolescent male with Rowell syndrome

  • R. A. Kadiru
  • , S. P. Hegde*
  • , H. K. Mithun
  • , A. C. Rao
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

A 15-year-old boy presented with fever, skin, and oral lesions for 4 weeks. The cutaneous lesions were suggestive of subacute cutaneous lupus erythematosus and erythema multiforme. His clinical, histopathological, and immunological features were indicative of Rowell syndrome and he satisfied the diagnostic criteria of Rowell syndrome proposed by Zeitouni et al. He subsequently developed neurological manifestations and was diagnosed to have neuropsychiatric systemic lupus erythematosus. We report this case for the unusual occurrence of a rare entity like Rowell syndrome in an adolescent male with co-existence of neuropsychiatric systemic lupus erythematosus.

Original languageEnglish
Pages (from-to)109-112
Number of pages4
JournalJournal of Postgraduate Medicine
Volume67
Issue number2
DOIs
Publication statusPublished - 01-04-2021

All Science Journal Classification (ASJC) codes

  • General Medicine

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