Literature DB >> 9736205

Pachymeningitis with multiple cranial neuropathies and unilateral optic neuropathy secondary to Pseudomonas aeruginosa: case report and review.

C A Girkin1, J D Perry, N R Miller, S G Reich.   

Abstract

Hypertrophic cranial pachymeningitis is a rare disorder that frequently presents with multiple cranial neuropathies. This disorder, which is characterized by thickening and infiltration of the cranial dura, can result from a variety of inflammatory and infectious conditions. A patient with hypertrophic cranial pachymeningitis is described in whom meningeal biopsy and bacterial cultures of the biopsy specimen revealed Pseudomonas aeruginosa. The authors believe this to be the first documented case of pachymeningitis secondary to this organism.

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Year:  1998        PMID: 9736205

Source DB:  PubMed          Journal:  J Neuroophthalmol        ISSN: 1070-8022            Impact factor:   3.042


  2 in total

1.  Hypertrophic cranial pachymeningitis and orbital apex syndrome secondary to infection of the eye: illustrative case.

Authors:  Tara Zielke; Miri Kim; Joshua E Simon; Ewa Borys; Vikram C Prabhu; Suguna Pappu
Journal:  J Neurosurg Case Lessons       Date:  2021-05-24

2.  Hypertrophic cranial pachymeningitis and skull base osteomyelitis by pseudomonas aeruginosa: case report and review of the literature.

Authors:  Ana Rita Caldas; Mariana Brandao; Filipe Seguro Paula; Elsa Castro; Fatima Farinha; Antonio Marinho
Journal:  J Clin Med Res       Date:  2012-03-23
  2 in total

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