ArticleMedicine2017
A case of idiopathic hypertrophic pachymeningitis presenting with chronic headache and multiple cranial nerve palsies: A case report.
Article in Medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 19 citations in OpenAlex.
- Idiopathic hypertrophic pachymeningitis masquerading as CNS neoplasm: case report and literature review.Immunologic research · 2026Review
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- Recurrent idiopathic hypertrophic pachymeningitis with chronic headache and cranial nerve involvement.Proceedings (Baylor University. Medical Center) · 2024Article
- Misleading Rare Case of Idiopathic Hypertrophic Pachymeningitis.Case reports in medicine · 2024Article
- Idiopathic hypertrophic pachymeningitis in a patient with a history of diffuse large B cell lymphoma.BMJ case reports · 2023Article
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- The Relationship Between Exacerbation of Pachymeningitis and Chemotherapy: A Case Report.Cureus · 2022Article
- An Update on Idiopathic Hypertrophic Cranial Pachymeningitis for the Headache Practitioner.Current pain and headache reports · 2020Review
- Hypertrophic chronic pachymeningitis associated with Epstein-Barr virus reactivation: a case report.Journal of neurovirology · 2019Article
- Case report: hypertrophic pachymeningitis associated with Sjögren's syndrome.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019Article
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
rationaleIdiopathic hypertrophic pachymeningitis (IHP) is a rare condition, characterized by a chronic fibrosing inflammatory process usually involving either the intracranial or spinal dura mater, but rarely both. Here, we report a rare case of IHP affecting both the intracranial and spinal dura mater. We also discussed the diagnosis, management, and outcome of IHP. PATIENT CONCERNS: We reviewed the case of a 60-year-old woman presenting with chronic headache, multiple cranial nerve palsies and gait disturbance. Magnetic resonance imaging (MRI) of her head revealed thickened and contrast-enhanced dura in the craniocervical region as well as obstructive hydrocephalus and cerebellar tonsillar herniation. The patient had a suboccipital craniectomy and posterior decompression through C1 plus a total laminectomy. The dura was partially resected to the extent of the bony decompression, and a duroplasty was performed. DIAGNOSES: Microscopic examination of the surgically resected sample showed chronic inflammatory changes, lymphoplasmacytic cell infiltration, fibrous tissue hyperplasia, and hyaline degeneration. Blood tests to evaluate the secondary causes of hypertrophic pachymeningitis (HP) were unremarkable.
interventionsSteroid was used to treat suspected IHP. OUTCOMES: Postoperatively, the patient showed gradual improvement in her headache, glossolalia, and bucking. Prior to discharge, a follow-up MRI showed improvement of the dura mater thickening. LESSONS: IHP is a chronic inflammatory disorder of the dura mater that usually causes neurological deficits. Clinical manifestations of IHP, MRI findings, and laboratory abnormalities are the essential components for making an accurate diagnosis. When the radiological or laboratory evaluation is uncertain, but neurological deficits are present, a prompt surgical approach should be considered. Postoperative steroid therapy and close observation for recurrence are necessary to ensure a good long-term outcome.
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