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1.
Rev. méd. Chile ; 146(11): 1356-1360, nov. 2018. graf
Artículo en Español | LILACS | ID: biblio-985711

RESUMEN

Giant cell arteritis is the most common vasculitis in patients aged over 50 years. We report an 89-year-old woman with significant weight loss and persistent frontal-occipital headaches lasting two months. The neurological examination at admission identified a decrease in visual acuity of the left eye, paralysis of the third cranial nerve of the right eye and alterations of body motility without objective signs of damage of the motor or sensitive pathways. Magnetic resonance imaging showed changes of the temporal artery wall and in both vertebral arteries, as well as bilateral cerebellar and occipital ischemic lesions. The Doppler ultrasound of the temporal arteries was compatible with Giant cell arteritis. Treatment with steroids was started. While receiving oral prednisone, the patient suffered new infarcts of the posterior territory, documented with a CAT scan.


Asunto(s)
Humanos , Femenino , Anciano de 80 o más Años , Arteritis de Células Gigantes/diagnóstico por imagen , Arteria Basilar/diagnóstico por imagen , Arteria Vertebral/diagnóstico por imagen , Enfermedades del Nervio Oculomotor/diagnóstico por imagen , Isquemia Encefálica/diagnóstico por imagen , Nervio Oculomotor/diagnóstico por imagen , Arterias Temporales/diagnóstico por imagen , Arteritis de Células Gigantes/etiología , Arteritis de Células Gigantes/patología , Arteria Basilar/patología , Arteria Vertebral/patología , Imagen por Resonancia Magnética/métodos , Enfermedades del Nervio Oculomotor/etiología , Enfermedades del Nervio Oculomotor/patología , Isquemia Encefálica/etiología , Isquemia Encefálica/patología , Ultrasonografía Doppler/métodos , Nervio Oculomotor/patología
2.
Neurol India ; 2006 Dec; 54(4): 437-9
Artículo en Inglés | IMSEAR | ID: sea-121394

RESUMEN

A 63-year-old woman presented with an extremely rare oculomotor schwannoma not associated with neurofibromatosis, manifesting as a transient diplopia and ptosis. Magnetic resonance images showed a well-enhanced mass extending from the cavernous sinus to the intraorbital region. Surgical exposure confirmed the tumor originating from the oculomotor nerve in the cavernous sinus. The intraorbital cystic part of the tumor was partially resected to preserve the oculomotor function. This is the first case of oculomotor schwannoma in the cavernous sinus with intraorbital component.


Asunto(s)
Blefaroptosis/etiología , Neoplasias de los Nervios Craneales/patología , Diplopía/etiología , Femenino , Humanos , Persona de Mediana Edad , Neurilemoma/patología , Enfermedades del Nervio Oculomotor/patología
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