BMC Neurology (Sep 2024)

Spinal cord compression by cystic IgG4-related spinal pachymeningitis mimicking neurocysticercosis: a case report

  • David Augusto Batista Sá Araújo¹,
  • Rodrigo Mariano Ribeiro,
  • Pedro Lucas Grangeiro Sá Barreto Lima,
  • Dánton Campos de Queiroz,
  • Milena Sales Pitombeira,
  • Bernardo Martins,
  • Pablo Picasso Araújo Coimbra,
  • Cleto Dantas Nogueira,
  • Pedro Braga-Neto,
  • Guilherme Diogo Silva,
  • Paulo Ribeiro Nóbrega

DOI
https://doi.org/10.1186/s12883-024-03817-7
Journal volume & issue
Vol. 24, no. 1
pp. 1 – 7

Abstract

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Abstract Background To report a case of IgG4-related pachymeningitis presenting with cystic lesions mimicking neurocysticercosis. Case presentation A 40-year-old female patient with tetraparesis, dysphagia and dysphonia was evaluated with clinical examination, magnetic resonance imaging, and meningeal biopsy. Magnetic resonance imaging (MRI) revealed diffuse pachymeningeal enhancement involving the cranial, cervical, thoracic, and lumbar segments with spinal cord compression and cystic lesions. CSF immunology was initially positive for cysticercus cellulosae. After disease progression a meningeal biopsy was compatible with IgG4 related disease. The patient had partial response to rituximab and needed multiple surgical procedures for spinal cord decompression and CSF shunting. Conclusions This case highlights the possibility of IgG4-related disease in patients with diffuse pachymeningitis causing spinal cord compression, even with cystic lesions on MRI. Diagnosis of IgG4-related pachymeningitis is paramount due to the possibility of treatment response to immunotherapy, particularly to anti-CD20 agents.

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