Intractable vomiting as the initial presentation of neuromyelitis optica

  • Metha Apiwattanakul
  • , Bogdan F. Popescu
  • , Marcelo Matiello
  • , Brian G. Weinshenker
  • , Claudia F. Lucchinetti
  • , Vanda A. Lennon
  • , Andrew McKeon
  • , Adam F. Carpenter
  • , Gary M. Miller
  • , Sean J. Pittock

Research output: Contribution to journalArticlepeer-review

Abstract

We report 12 aquaporin-4 antibody-positive patients (12% of seropositive Mayo Clinic patients identified since 2005) whose initial presenting symptom of neuromyelitis optica was intractable vomiting. The initial evaluation in 75% was gastroenterologic. Vomiting lasted a median of 4 weeks (range, 2 days-80 weeks). Optic neuritis or transverse myelitis developed after vomiting onset in 11 patients (median interval, 11 weeks; range, 1-156). At last evaluation (median, 48 months after vomiting onset), 7 patients fulfilled neuromyelitis optica diagnostic criteria. Our clinical, pathologic and neuroimaging observations suggest the aquaporin-4-rich area postrema may be a first point of attack in neuromyelitis optica. Ann Neurol 2010;68:757-761

Original languageEnglish (US)
Pages (from-to)757-761
Number of pages5
JournalAnnals of Neurology
Volume68
Issue number5
DOIs
StatePublished - Nov 2010

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