Anti-Ma encephalitis masquerading as Wernicke encephalopathy

Huanyu Meng1, Qinming Zhou1, Sheng Chen1

  • 1Ruijin Hospital, Department of Neurology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Abstract

Insights

Anti-Ma encephalitis, a rare autoimmune disorder, can mimic Wernicke encephalopathy. Early suspicion is crucial, especially when Vitamin B1 treatment fails in patients with neurological symptoms and potential cancer.

Area of Science:

  • Neurology
  • Oncology
  • Immunology

Background:

  • Anti-Ma encephalitis is typically linked to testicular cancer in young males.
  • Gastric cancer association with Anti-Ma encephalitis presenting as Wernicke encephalopathy-like symptoms is uncommon.
  • This report details a rare case in an elderly patient initially misdiagnosed.

Observation:

  • A 71-year-old male with alcohol abuse presented with dizziness, diplopia, and anorexia.
  • Initial Wernicke encephalopathy diagnosis and Vitamin B1 treatment were ineffective.
  • Detection of anti-Ma1/2 antibodies in blood and CSF confirmed the diagnosis.

Findings:

  • 18F-FDG PET-MR revealed hypermetabolic changes in the hypothalamus, basal ganglia, and brainstem.
  • Gastric neoplasms with liver metastasis were identified.
  • The patient was diagnosed with Anti-Ma encephalitis.

Implications:

  • Anti-Ma encephalitis should be considered in patients with Wernicke encephalopathy-like symptoms unresponsive to Vitamin B1.
  • This case highlights the importance of antibody testing for accurate diagnosis.
  • Timely diagnosis and treatment are crucial for managing this rare autoimmune encephalitis.