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1.
West Indian med. j ; 38(3): 171-5, Sept. 1989.
Artigo em Inglês | MedCarib | ID: med-14288

RESUMO

A case of an abscess of the sella turcica discovered during craniotomy for pituitary tumour in a 20-year-old man is presented. The clinical features of this unusual intrasellar lesion are discussed. The importance of early diagnosis, high-dosage antibiotics and surgical intervention in reducing the high mortality associated with abscesses in this location are emphasized. It is suggested that abscess of the sella turcia should be considered in the differential diagnosis of a sella mass in any patient with a recent history of cerebrospinal fluid rhinorrhea, sphenoid sinusitis or meningitis (AU)


Assuntos
Adulto , Humanos , Masculino , Abscesso Encefálico/diagnóstico , Sela Túrcica , Diagnóstico Diferencial , Abscesso Encefálico/patologia , Abscesso Encefálico/cirurgia
2.
West Indian med. j ; 35(3): 203-5, Sept. 1986.
Artigo em Inglês | MedCarib | ID: med-11574

RESUMO

A case of ischaemic spinal cord injury in a 70-year old patient is presented. Autopsy showed a DeBakey type 1 dissecting aneurysm of the thoraco-abdominal aorta with involvement of the intercostal and lumbar arteries on the left side. The zone of spinal cord infarction was extensive. The vascular anatomy of the spinal cord is reviewed, and its vulnerability to ischaemia is emphazied (AU)


Assuntos
Humanos , Dissecção Aórtica/diagnóstico , Aneurisma Aórtico/diagnóstico , Infarto/diagnóstico , Medula Espinal/irrigação sanguínea , Aorta Abdominal , Aorta Torácica
3.
West Indian med. j ; 34(2): 131-3, June 1985.
Artigo em Inglês | MedCarib | ID: med-11541

RESUMO

A unique case of sporadic concurrence of von Recklinghausen's neurofibromatosis parentage and normal family background is described. The pathogenetic aspects of this rare phenomenon are discussed. It is suggested that such an unusual concurrence is the result of spontaneous genetic mutation (AU)


Assuntos
Adulto , Masculino , Feminino , Neurofibromatoses/complicações , Síndrome de Marfan/complicações , Neurofibromatoses/genética , Síndrome de Marfan/genética , Jamaica
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