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[Case of isolated neurosarcoidosis requiring differentiation from tuberculous meningitis].
Deguchi, Ichiro; Osada, Takashi; Suzuki, Tomonari; Tabata, Shinya; Arai, Eiichi; Uchino, Akira; Hayashi, Takeshi; Takahashi, Shinichi; Momoshima, Suketaka; Takao, Masaki.
Afiliação
  • Deguchi I; Department of Neurology and Cerebrovascular Medicine, Saitama Medical University International Medical Center.
  • Osada T; Department of Neurology and Cerebrovascular Medicine, Saitama Medical University International Medical Center.
  • Suzuki T; Department of Neuro-Oncology/Neurosurgery, Saitama Medical University International Medical Center.
  • Tabata S; Department of Neuro-Oncology/Neurosurgery, Saitama Medical University International Medical Center.
  • Arai E; Department of Pathology, Saitama Medical University International Medical Center.
  • Uchino A; Department of Diagnostic Radiology, Saitama Medical University International Medical Center.
  • Hayashi T; Department of Neurology and Cerebrovascular Medicine, Saitama Medical University International Medical Center.
  • Takahashi S; Department of Neurology and Cerebrovascular Medicine, Saitama Medical University International Medical Center.
  • Momoshima S; Center for Preventive Medicine, Keio University School of Medicine.
  • Takao M; Department of Neurology and Cerebrovascular Medicine, Saitama Medical University International Medical Center.
Rinsho Shinkeigaku ; 60(3): 213-218, 2020 Mar 31.
Article em Ja | MEDLINE | ID: mdl-32101846
A 62-year-old woman was transported to our hospital for management of generalized clonic seizures. Cerebrospinal fluid examination showed an increased monocyte-dominant cell count, high protein concentration, and low glucose concentration that was 17% of the plasma glucose concentration. Contrast-enhanced cranial magnetic resonance imaging revealed diffuse leptomeningeal enhancement with multiple nodular lesions. She underwent examinations that ruled out the following conditions: tuberculous meningitis, systemic sarcoidosis, malignant lymphoma, carcinomatous meningitis, and central nervous system vasculitis. On hospital day 13, dural and brain biopsies revealed neurosarcoidosis, for which steroid therapy was administered. Thereafter, imaging examinations showed marked improvement. Because isolated neurosarcoidosis is difficult to diagnose, early pathologic diagnosis may be essential.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoidose / Tuberculose Meníngea / Encéfalo / Doenças do Sistema Nervoso Central Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Female / Humans / Middle aged Idioma: Ja Revista: Rinsho Shinkeigaku Ano de publicação: 2020 Tipo de documento: Article País de publicação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoidose / Tuberculose Meníngea / Encéfalo / Doenças do Sistema Nervoso Central Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Female / Humans / Middle aged Idioma: Ja Revista: Rinsho Shinkeigaku Ano de publicação: 2020 Tipo de documento: Article País de publicação: Japão