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Signal Void Dots on T2-weighted Brain MR Image: Correlation with Hypertensive Brain lesions
Journal of the Korean Radiological Society ; : 647-652, 1998.
Artículo en Coreano | WPRIM | ID: wpr-166584
ABSTRACT

PURPOSE:

To evaluate the relationship of signal void dots seen on T2-weighted images with hypertension,hypertensive intracerebral hemorrhage and infarction. MATERIALS AND

METHODS:

MR images of 73 consecutive patientswith signal void dots on T2-weighted images were reviewed. Seventy-three randomly selected age-matched patientswithout signal void dot lesion were also reviewed. We evaluated 1) the location and number of signal void dots; 2)the frequency of hypertension among patients and controls; 3) the frequency of associated brain parenchymalabnormalities (hypertensive intracerebral hemorrhage, microangiopathy and infarction) in both groups; 4) therelationship between the number of signal void dots and associated brain lesions in the patient group.

RESULTS:

Signal void dots numbered 1-50(average, 12), and were found mostly in the thalamus, basal ganglia, and the pons.Hypertension(97.1%), hypertensive ICH(43.8%) and microangiopathy(96%) were frequent in patients with signal voiddots, the number of which correlated with the severity of microangiopathy. Infarction(13.7%), however, did notcorrelate with dots.

CONCLUSION:

Signal void dots correlate closely with hypertension, hypertensive ICH, andmicroangiopathy. They may indicate hypertensive brain change.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Tálamo / Ganglios Basales / Encéfalo / Hemorragia Cerebral / Hipertensión / Infarto Límite: Humanos Idioma: Coreano Revista: Journal of the Korean Radiological Society Año: 1998 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Tálamo / Ganglios Basales / Encéfalo / Hemorragia Cerebral / Hipertensión / Infarto Límite: Humanos Idioma: Coreano Revista: Journal of the Korean Radiological Society Año: 1998 Tipo del documento: Artículo