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March 3, 2026Journal of Pediatric Neurology0 citationsOpen Access

Area Postrema Syndrome as The Onset of Neuromyelitis Optica in a Pediatric Patient: Case Report

JAJuan Martín Mancera AlzateHospital Universitario del Valle ESETHTaina Yubelys Brito HurtadoCCChristian Andrés Rojas CerónHospital Universitario del Valle ESE

Key Points

  • Intractable vomiting was found to be linked to demyelination in the area postrema, suggesting a rare presentation.
  • MRI results revealed longitudinally extensive myelitis in the cervical and thoracic spine, prompting concern for serious neurological conditions.
  • Assessment of serum antibodies showed positive results for anti-aquaporin 4, a marker associated with neuromyelitis optica.
  • Highlighting the importance of considering neuromyelitis optica in pediatric patients presenting with intractable vomiting emphasizes diagnostic vigilance.

Abstract

Introduction: Area postrema syndrome, characterized by nausea, emesis, and persistent hiccups can be initial manifestation of demyelinating diseases of the central nervous system. Clinical case: we report a 4-year-old girl who presented with intractable vomiting that was noted to have signs of demyelination in the area postrema. MRI spine revealed longitudinally extensive myelitis in the cervical and thoracic spine. Neuromyelitis optica spectrum disorder was suspected. Serum anti-aquaporin 4 antibodies were positive. Oligoclonal bands in cerebrospinal fluid were negative. Conclusion: Neuromyelitis optica spectrum disorders are extremely rare in the pediatric population, this being the second case reported in Colombia. . It’s crucial to consider the possibility of such neurological disorders in the setting of intractable vomiting.

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Cite This Study

Alzate et al. (2026) studied this question.

synapsesocial.com/papers/69a75ec2c6e9836116a29a7chttps://doi.org/10.53391/1875-9041.1015
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