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

Author:

Araújo David Augusto Batista Sá1,Ribeiro Rodrigo Mariano1,Lima Pedro Lucas Grangeiro de Sá Barreto1,Queiroz Dánton Campos1,Pitombeira Milena Sales2,Martins Bernardo3,Coimbra Pablo Picasso Araújo2,Nogueira Cleto Dantas4,Neto Pedro Braga5,Silva Guilherme Diogo6,Nóbrega Paulo Ribeiro5

Affiliation:

1. Faculty of Medicine, Federal University of Ceara

2. Department of Neurology, General Hospital of Fortaleza

3. Rede SARAH de Hospitais de Reabilitação

4. Laboratório Argos

5. Division of Neurology, Department of Clinical Medicine, Federal University of Ceara

6. Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

Abstract

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.

Publisher

Research Square Platform LLC

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