# Intractable Nausea as the Initial Presentation of Neuromyelitis Optica

**Authors:** Shu Jun Tan

PMC · DOI: 10.7759/cureus.103669 · Cureus · 2026-02-15

## TL;DR

A rare neurological condition was misdiagnosed due to persistent nausea and vomiting, highlighting the importance of considering NMOSD in such cases.

## Contribution

This case report highlights NMOSD as an under-recognized cause of intractable nausea and vomiting.

## Key findings

- NMOSD can present with persistent vomiting and nausea due to brainstem involvement.
- Diagnosis was confirmed through MRI and detection of AQP4 IgG antibodies.
- Treatment with steroids and tocilizumab led to significant improvement in symptoms.

## Abstract

Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune condition of the central nervous system, primarily involving the optic nerves and spinal cord. Patients typically present with visual disturbance, limb weakness or sensory deficits, and bladder dysfunction. However, atypical and nonspecific presentations may occur, including persistent nausea and vomiting due to involvement of the area postrema.

We report the case of a 26-year-old female patient who presented with a one-month history of intractable vomiting, associated with epigastric discomfort (worse prior to vomiting), reduced appetite, and significant weight loss of approximately 7-8 kg over one month. She had been admitted two times prior to presentation, with extensive investigations that were unremarkable.

During admission, she also reported blurred vision and was noted to have horizontal nystagmus. Brain MRI demonstrated areas of altered signal intensity involving the brainstem and cervicomedullary junction, along the floor of the fourth ventricle, initially raising concern for Wernicke’s encephalopathy. She received intravenous thiamine without clinical improvement. Further evaluation, including whole-spine MRI and autoimmune serology, revealed positivity for aquaporin-4 (AQP4) IgG antibodies, confirming NMOSD. She was treated with intravenous methylprednisolone and tocilizumab, resulting in marked symptomatic improvement.

This case highlights NMOSD as an important and often under-recognized cause of intractable nausea and vomiting, which may delay diagnosis and treatment. A thorough neurological history and examination are essential in patients with persistent unexplained vomiting to ensure timely recognition and initiation of appropriate therapy.

## Linked entities

- **Proteins:** AQP4 (aquaporin 4)
- **Diseases:** Neuromyelitis optica spectrum disorder (MONDO:0019100), Wernicke’s encephalopathy (MONDO:0007020)

## Full-text entities

- **Genes:** AQP4 (aquaporin 4) [NCBI Gene 361] {aka MIWC, MLC4, WCH4, hAQP4}
- **Diseases:** Wernicke's encephalopathy (MESH:D014899), Nausea (MESH:D009325), sensory deficits (MESH:D012678), nausea and vomiting (MESH:D020250), limb weakness (MESH:D018908), weight loss (MESH:D015431), blurred vision (MESH:D014786), autoimmune (MESH:D001327), horizontal nystagmus (MESH:D009759), vomiting (MESH:D014839), NMOSD (MESH:D009471), bladder dysfunction (MESH:D001745)
- **Chemicals:** methylprednisolone (MESH:D008775), tocilizumab (MESH:C502936), thiamine (MESH:D013831)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12995520/full.md

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Source: https://tomesphere.com/paper/PMC12995520