Hypertrophic cervical spine pachymeningitis due to sarcoidosis: a case report.
Adult
Biopsy
Cervical Vertebrae
/ pathology
Decompression, Surgical
/ methods
Dura Mater
/ pathology
Female
Humans
Laminectomy
/ methods
Magnetic Resonance Imaging
Meningitis
/ diagnostic imaging
Sarcoidosis
/ diagnostic imaging
Spinal Cord Compression
/ diagnostic imaging
Steroids
/ administration & dosage
Treatment Outcome
Hypertrophic pachymeningitis
case report
cervical spine
myelopathy
sarcoidosis
spinal cord compression
Journal
Hospital practice (1995)
ISSN: 2154-8331
Titre abrégé: Hosp Pract (1995)
Pays: England
ID NLM: 101268948
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
pubmed:
27
1
2019
medline:
18
4
2019
entrez:
27
1
2019
Statut:
ppublish
Résumé
Hypertrophic pachymeningitis (HP) is a chronic, progressive diffuse inflammatory condition that leads to thickening of the dura mater and can be idiopathic or associated with sarcoidosis among other disorders. In this case report, we present a rare case of cervical spine HP in a 29-year-old woman in the post-partum period, who had a history of pituitary adenoma and juvenile rheumatoid arthritis. Magnetic resonance imaging (MRI) of the spine revealed a soft tissue mass and moderate cord compression. The patient underwent C3-C7 laminectomy. Pathological analysis of the cervical epidural mass demonstrated a reactive inflammatory cell process. Recurrence of symptoms and worsening of pachymeningitis on imaging studies warranted further work-up which revealed mediastinal/hilar lymphadenopathy. Transbronchial biopsy revealed non-caseating granulomatous disease consistent with sarcoidosis. The patient was started on oral steroids and eventually methotrexate with significant clinical and radiographic improvement. Follow-up imaging studies showed minimal dural thickening in the thoracic spine and eventually complete resolution. HP should be considered in a patient with spinal cord compression, myelopathy, and radicular pain of unclear etiology, and sarcoidosis should be considered in idiopathic cases.
Identifiants
pubmed: 30682899
doi: 10.1080/21548331.2019.1575645
doi:
Substances chimiques
Steroids
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM