Literature DB >> 3389076

[Multiple cranial nerve involvement associated with tentorial pachymeningitis of granulomatous type].

S Ghilain1, V Delreux, L Kevers, C J Sindic, P Mathurin, E C Laterre.   

Abstract

Otitis media in a 43 year-old male patient was followed by signs of chronic meningitis with persistent headaches, moderate pleiomorphic lymphocytosis of CSF without hypoglycorrhachia and unilateral impairment of cranial nerves XI to II. These signs were accompanied by widespread inflammation with general deterioration of the patient's condition. After a time the tentorium of cerebellum showed thickening and significant contrast uptake in conjunction with necrotizing granulomatous inflammation, indicating tentorial pachymeningitis. Swift and complete remission was obtained with a corticoid-cyclophosphamide combination. After reviewing the other possible causes of chronic meningitis, the authors proposed a diagnosis of Wegener's disease of auricular origin in view of the compatibility of all the data. A few cases of cranial pachymeningitis of indeterminate origin are described in the literature. Only this patient was treated with a corticoid-cyclophosphamide combination. The remarkable efficacy of this double therapy confirms the diagnostic hypothesis of Wegener's granulomatosis.

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Year:  1988        PMID: 3389076

Source DB:  PubMed          Journal:  Acta Neurol Belg        ISSN: 0300-9009            Impact factor:   2.396


  1 in total

Review 1.  Idiopathic intracranial hypertrophic pachymeningitis: two case reports and review of the literature.

Authors:  Giancarlo D'Andrea; Giuseppe Trillò; Paolo Celli; Raffaelino Roperto; Francesco Crispo; Luigi Ferrante
Journal:  Neurosurg Rev       Date:  2004-03-06       Impact factor: 3.042

  1 in total

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