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Spinal cord compression by cystic IgG4-related spinal pachymeningitis mimicking neurocysticercosis: a case report
David Augusto Batista Sá Araújo1, Rodrigo Mariano Ribeiro1, Pedro Lucas Grangeiro Sá Barreto Lima1
1Faculty of Medicine, Federal University of Ceara, Alexandre Baraúna St., 949, Fortaleza, 60430-160, Ceara, Brazil.
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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