A diagnostic challenge in a young woman with intractable hiccups and vomiting: a case of neuromyelitis optica

Intractable nausea and vomiting along with hiccups is a commonly encountered problem on any general medicine or gastroenterology service. These symptoms are usually not appreciated as the possible initial manifestation of neuromyelitis optica (NMO). Missing diagnosis at this early stage will lead to a delay in the treatment, and hence, irreversible complications including blindness and paraplegia could occur. We report a case of a 22-year-old young female who presented with intractable hiccups and vomiting. After extensive evaluation, she was found to have NMO which involved the area postrema, the vomiting center of the brain. Early diagnosis from the clinical picture aided by aquaporin-4 serologic testing is extremely important to allow early initiation of immunosuppressive therapy. Immunosuppression gives an opportunity to modify the disease at an earlier stage rather than waiting for evolution of disease to fulfill the diagnostic criteria of NMO.

[1]  K. Fujihara,et al.  Pregnancy-related relapse risk factors in women with anti-AQP4 antibody positivity and neuromyelitis optica spectrum disorder , 2016, Multiple sclerosis.

[2]  Jae-Hyun Park,et al.  Presence of anti-Ro/SSA antibody may be associated with anti-aquaporin-4 antibody positivity in neuromyelitis optica spectrum disorder , 2015, Journal of the Neurological Sciences.

[3]  R. Ferguson Rapid assessment of health literacy on admission to the hospital , 2015, Journal of community hospital internal medicine perspectives.

[4]  R. Balabanov,et al.  Immunotherapy of Neuromyelitis Optica , 2013, Autoimmune diseases.

[5]  F. Paul,et al.  Update on the diagnosis and treatment of neuromyelitis optica: Recommendations of the Neuromyelitis Optica Study Group (NEMOS) , 2013, Journal of Neurology.

[6]  P. Pasricha,et al.  Intractable nausea and vomiting from autoantibodies against a brain water channel. , 2013, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

[7]  H. Kim,et al.  Clinical spectrum of CNS aquaporin-4 autoimmunity , 2012, Neurology.

[8]  A. Carpenter,et al.  Intractable vomiting as the initial presentation of neuromyelitis optica , 2010, Annals of neurology.

[9]  S. Ito POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME IN NEUROMYELITIS OPTICA SPECTRUM DISORDERS , 2009, Neurology.

[10]  B. Weinshenker,et al.  The spectrum of neuromyelitis optica , 2007, The Lancet Neurology.

[11]  J. Parisi,et al.  Pattern-specific loss of aquaporin-4 immunoreactivity distinguishes neuromyelitis optica from multiple sclerosis. , 2007, Brain : a journal of neurology.

[12]  A. Brown Neuromyelitis Optica IgG Predicts Relapse after Longitudinally Extensive Transverse MyelitisWeinshenker BG, Wingerchuk DM, Vukusic S, et al (Mayo Clinic, Rochester, Minn; Mayo Clinic, Scottsdale, Ariz; Hopital Neurologique, Lyon, France) Ann Neurol 59:566–569, 2006§ , 2007 .

[13]  S. Vukusic,et al.  Neuromyelitis optica IgG predicts relapse after longitudinally extensive transverse myelitis , 2006, Annals of neurology.