| Literature DB >> 21031587 |
Metha Apiwattanakul1, 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.
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.Entities:
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Year: 2010 PMID: 21031587 DOI: 10.1002/ana.22121
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422