Area postrema syndrome: An unusual presentation of neuromyelitis optica spectrum disorder

Author:

Raj Aiswarya1,Valappil Ashraf V.1,Alapatt Paul J.1,Kamar Jubin2

Affiliation:

1. Department of Neurology, Aster MIMS Hospital, Kozhikode, Kerala, India,

2. Department of Gastroenterology, Aster MIMS Hospital, Kozhikode, Kerala, India,

Abstract

Isolated area postrema syndrome (APS) is a rare neurological presentation of, neuromyelitis optica spectrums disorder (NMOSD), recognizable by uncontrollable hiccups, nausea, or vomiting. When it occurs as the first presentation of NMOSD, it may present as a diagnostic challenge as the condition may be frequently attributed to gastrointestinal pathology, and the subsequent diagnostic delay may result in debilitating neurological sequelae such as optic neuritis or myelitis. We report such a case of isolated APS in a young woman who presented with a clinical picture of bouts of vomiting and intractable hiccups causing considerable distress and was finally diagnosed to be a case of seronegative NMOSD.

Publisher

Scientific Scholar

Subject

Neurology (clinical),General Neuroscience

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