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2.
J Clin Neuroophthalmol ; 3(4): 239-44, 1983 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-6232288

RESUMEN

We report three patients who developed symptomatic visual loss following uncomplicated general surgical procedures. All three patients had ocular examinations and visual field deficits consistent with acute ischemic optic neuropathy. All three had hemoglobin levels below normal limits at the onset of visual symptoms. However, none of the patients suffered intraoperative or postoperative hemorrhaging. Ischemic optic neuropathy may occur following general surgical procedures, not complicated by significant hemorrhaging.


Asunto(s)
Isquemia/etiología , Enfermedades del Nervio Óptico/etiología , Nervio Óptico/irrigación sanguínea , Trastornos de la Visión/etiología , Adolescente , Adulto , Transfusión Sanguínea , Puente de Arteria Coronaria , Femenino , Fondo de Ojo , Hemorragia Gastrointestinal/complicaciones , Hemorragia Gastrointestinal/etiología , Humanos , Isquemia/terapia , Trasplante de Riñón , Masculino , Persona de Mediana Edad , Enfermedades del Nervio Óptico/terapia , Glándulas Paratiroides/cirugía , Complicaciones Posoperatorias/etiología , Hemorragia Uterina/complicaciones , Hemorragia Uterina/etiología , Trastornos de la Visión/terapia
3.
Ophthalmology ; 90(11): 1373-7, 1983 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-6664678

RESUMEN

Neuronal ceroid lipofuscinosis (NCL), or Batten-Vogt's disease, is a disorder of young children who manifest visual, neurologic, and mental problems. The ophthalmologist can provide helpful diagnostic information by examining the fundus and performing an electroretinogram. In addition, diagnostic markers can be identified by examining circulating lymphocytes from a peripheral blood specimen with light and electron microscopy.


Asunto(s)
Oftalmopatías/diagnóstico , Linfocitos/ultraestructura , Lipofuscinosis Ceroideas Neuronales/diagnóstico , Niño , Preescolar , Electrorretinografía , Femenino , Fondo de Ojo , Humanos , Lipidosis/clasificación , Microscopía Electrónica , Lipofuscinosis Ceroideas Neuronales/sangre
4.
Ann Ophthalmol ; 14(8): 717-20, 1982 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-7125466

RESUMEN

We have presented a case of Wegener's granulomatosis with characteristic systemic and ocular manifestations. The diagnosis was determined pathologically by thoracotomy and lung biopsy. Our patient's ocular complications included an intense vitritis, exudative retinal detachment, choroiditis, and other corneoscleral manifestations. Exudative retinal detachment is a finding not previously described clinically, but alluded to in pathologic descriptions from case reports. Both systemic and ocular response were obtained within weeks after the patient started cyclophosphamide and prednisone. In addition to recording this new finding, we have reviewed the pathology and ocular manifestations of this uncommon disorder, outlined a modern therapeutic protocol, and updated the present-day prognosis of Wegener's granulomatosis.


Asunto(s)
Granulomatosis con Poliangitis/complicaciones , Desprendimiento de Retina/complicaciones , Ciclofosfamida/uso terapéutico , Granulomatosis con Poliangitis/tratamiento farmacológico , Humanos , Masculino , Persona de Mediana Edad , Prednisona/uso terapéutico , Desprendimiento de Retina/diagnóstico , Desprendimiento de Retina/tratamiento farmacológico , Ultrasonografía
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