Neuromyelitis Optica Spectrum Disorder Manifested by Persistent Hiccups and Severe Esophagitis in an Adolescent

Priya Singh1, Reinaldo Garcia1,2, Madhura Y Phadke3

  • 1From the Northeast Ohio Medical University, Rootstown, OH.

JPGN Reports
|May 19, 2023
PubMed

Insights

Persistent hiccups in an 18-year-old male were initially attributed to esophagitis but were ultimately diagnosed as a symptom of neuromyelitis optica spectrum disorder, a rare autoimmune condition.

Area of Science:

  • Neurology
  • Gastroenterology
  • Immunology

Background:

  • Persistent hiccups are often evaluated by gastroenterologists, with causes spanning multiple organ systems.
  • Hiccups exceeding 48 hours are classified as persistent, and those over 2 months as intractable.

Observation:

  • An 18-year-old male presented with persistent hiccups, nausea, and emesis, initially diagnosed with severe esophagitis.
  • Despite gastrointestinal treatment, hiccups worsened, prompting a neurological consultation.
  • Brain MRI revealed a dorsal medullary lesion, leading to the diagnosis of neuromyelitis optica spectrum disorder.

Findings:

  • Neuromyelitis optica spectrum disorder is a rare, severe autoimmune central nervous system condition.
  • Early diagnosis and treatment are crucial for managing relapses in neuromyelitis optica spectrum disorder.
  • The patient experienced rapid symptom improvement with high-dose intravenous steroids.

Implications:

  • This case highlights the importance of considering neurological etiologies for hiccups, especially when gastrointestinal causes are unresponsive to treatment.
  • It underscores the need for a multidisciplinary approach, integrating neurology and gastroenterology, for complex cases.
  • Prompt neurological evaluation can lead to timely diagnosis and management of rare autoimmune disorders presenting with atypical symptoms.

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