Autoimmune sensorineural hearing loss/Meniere's disease possibly triggered by neurocysticercosis: a case report

Hamza Arman Lateef1, Evan Davies2, Alidad Arabshahi3

  • 1Harvard College, Cambridge, MA, US. armanlateef@college.harvard.edu.

PubMed
Abstract

Insights

This case report suggests neurocysticercosis may trigger Meniere's disease. Further examination is needed to identify coexisting neurological conditions in Meniere's disease patients.

Area of Science:

  • Neurology
  • Otolaryngology
  • Infectious Diseases

Background:

  • Meniere's disease is characterized by inner ear fluid imbalance, causing vertigo, tinnitus, and hearing loss.
  • Known triggers include lifestyle factors and infections, but parasitic disease links are undocumented.
  • This study explores an atypical presentation of Meniere's disease.

Purpose of the Study:

  • To report a unique case of Meniere's disease potentially linked to neurocysticercosis.
  • To highlight the importance of thorough patient evaluation for neurological comorbidities.

Main Methods:

  • A 37-year-old male with Meniere's disease symptoms underwent clinical and laboratory evaluation.
  • Diagnostic tools included electrocochleography, vestibulonystagmography, and brain MRI.
  • Patient history revealed a prior tapeworm infection.

Main Results:

  • The patient exhibited Meniere's disease symptoms and positive anti-heat shock proteins antibody.
  • Neuroimaging revealed postinflammatory calcification and volume loss, indicative of neurocysticercosis.
  • Standard Meniere's disease treatments were ineffective.

Conclusions:

  • This is the first reported instance suggesting Meniere's disease may be triggered by or concurrent with neurocysticercosis.
  • Comprehensive neurological assessments are crucial for patients with Meniere's disease.
  • Parasitic infections should be considered in the differential diagnosis.

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