Journal of Craniovertebral Junction and Spine (Jan 2017)

Idiopathic hypertrophic pachymeningitis as a rare cause of cervical compressive myelopathy

  • Aya Fukuda,
  • Elizabete Punaro,
  • Fábio Rogério,
  • Luciano de Souza Queiroz,
  • Fabiano Reis

DOI
https://doi.org/10.4103/jcvjs.JCVJS_118_17
Journal volume & issue
Vol. 8, no. 4
pp. 387 – 389

Abstract

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The spinal form of idiopathic hypertrophic pachymeningitis (IHP) is a rare condition characterized by a chronic progressive diffuse inflammatory fibrosis of the dura mater, which may evolve to the compression of the spinal cord. We present a case report about IHP focusing on its features in magnetic resonance imaging, which are determined by an intradural extramedullary mass in the cervical spine showing hypointensity on T2-weighted images and peripheral enhancement, causing compression of the spinal cord. Histological analysis showed a nonspecific chronic inflammatory process in dense fibrous tissue. The patient had a good outcome after therapy with steroids.

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