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Neurofibromatosis, stroke and basilar impression: case report
Piovesan, Elcio Juliato; Scola, Rosana Herminia; Werneck, Lineu Cesar; Zétola, Viviane H. Flumignan; Nóvak, Edison Matos; Iwamoto, Fabio Massaiti; Piovesan, Liciane Maia.
  • Piovesan, Elcio Juliato; Universidade Federal do Paraná. Hospital de Clínicas. Departamento de Medicina Interna.
  • Scola, Rosana Herminia; Universidade Federal do Paraná. Hospital de Clínicas. Departamento de Medicina Interna.
  • Werneck, Lineu Cesar; Universidade Federal do Paraná. Hospital de Clínicas. Departamento de Medicina Interna.
  • Zétola, Viviane H. Flumignan; Universidade Federal do Paraná. Hospital de Clínicas. Departamento de Medicina Interna.
  • Nóvak, Edison Matos; Universidade Federal do Paraná. Hospital de Clínicas. Departamento de Medicina Interna.
  • Iwamoto, Fabio Massaiti; Universidade Federal do Paraná. Hospital de Clínicas. Departamento de Medicina Interna.
  • Piovesan, Liciane Maia; Universidade Federal do Paraná. Hospital de Clínicas. Departamento de Medicina Interna.
Arq. neuropsiquiatr ; 57(2B): 484-8, jun. 1999. ilus, tab
Article in English | LILACS | ID: lil-236079
ABSTRACT
Neurofibromatosis type (NF1) can virtually affect any organ, presenting most frequently with "cafe au lait" spots and neurofibromas. Vasculopathy is a known complication of NF1, but cerebrovascular disease is rare. We report the case of a 51-year-old man admitted to the hospital with a history of stroke four months before admission. On physical examination, he presented various "cafe au lait" spots and cutaneous neurofibromas. Neurologic examination demonstrated right-sided facial paralysis, right-sided hemiplegia, and aphasia. Computed tomography scan of head showed hypodense areas in the basal ganglia and centrum semiovale. Radiographs of cranium and cervical spine showed basilar impression. Angiography revealed complete occlusion of both vertebral and left internal carotid arteries, and partial stenosis of the right internal carotid artery. A large network of collateral vessels was present (moyamoya syndrome). It is an uncommon case of occlusive cerebrovascular disease associated with NF1, since most described in the literature are in young people, and tend to spare the posterior cerebral circulation. Basilar impression associated with this case may be considered a pure coincidence, but rare cases of basilar impression and NF1 have been described.
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Platybasia / Cerebrovascular Disorders / Neurofibromatosis 1 Type of study: Diagnostic study Limits: Humans / Male Language: English Journal: Arq. neuropsiquiatr Journal subject: Neurology / Psychiatry Year: 1999 Type: Article

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Full text: Available Index: LILACS (Americas) Main subject: Platybasia / Cerebrovascular Disorders / Neurofibromatosis 1 Type of study: Diagnostic study Limits: Humans / Male Language: English Journal: Arq. neuropsiquiatr Journal subject: Neurology / Psychiatry Year: 1999 Type: Article