dc.creator | López-Rodríguez,Raimundo | |
dc.creator | García-González,Jorge | |
dc.creator | Campos-Franco,Joaquín | |
dc.creator | Mallo-González,Nieves | |
dc.creator | Alende-Sixto,María Rosario | |
dc.date | 2007-07-01 | |
dc.date.accessioned | 2017-03-07T15:51:48Z | |
dc.date.available | 2017-03-07T15:51:48Z | |
dc.identifier | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872007000700012 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/392121 | |
dc.description | Wegener's granulomatosis is a systemic necrotizing vasculitis that affects medium size and small vessels. Neurological involvement occurs in 22% to 54% of patients, mainly in the form of mononeuritis multiplex. Central nervous system involvement is reported in only 2% to 8% of the cases. We report a 42-year-old male who presented with headache, diplopia, third and sixth cranial nerve palsies and ¡eft eye amaurosis associated to mass located in the ¡eft Meckel cavum and diffuse meningeal involvement. A biopsy of the mass disclosed a chronic granulomatous necrotizing inflammation with Langhans giant cells. A chest CAT scan showed three cavitated lung nodules and ANCA antibodies were positive in a titer of 1:80. Treatment with steroid and cyclophosphamide was started and cranial nerve palsies resolved and the number and size of lung nodules decreased. The patient was lost from follow up | |
dc.format | text/html | |
dc.language | es | |
dc.publisher | Sociedad Médica de Santiago | |
dc.source | Revista médica de Chile v.135 n.7 2007 | |
dc.subject | Meningitis aseptic | |
dc.subject | Vasculitis | |
dc.subject | Wegener granulomatosis | |
dc.title | Manifestaciones neurológicas de la granulomatosis de Wegener: Caso clínico | |
dc.type | Artículos de revistas | |