Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
1.
Investigative Magnetic Resonance Imaging ; : 193-196, 2021.
Artículo en Inglés | WPRIM | ID: wpr-891150

RESUMEN

Congenital absence of the bilateral internal carotid arteries (ICA) is a very rare occurrence. Recognition of this rare anomaly is important, when considering intracranial endovascular interventions in the event of thromboembolic events with revascularization, transsphenoidal surgery, and the surveillance and detection of associated cerebral aneurysms. We report a case of a 25-year-old man who presented with headache since 2 years ago, and was incidentally discovered to have a congenital bilateral absence of ICAs.

2.
Investigative Magnetic Resonance Imaging ; : 193-196, 2021.
Artículo en Inglés | WPRIM | ID: wpr-898854

RESUMEN

Congenital absence of the bilateral internal carotid arteries (ICA) is a very rare occurrence. Recognition of this rare anomaly is important, when considering intracranial endovascular interventions in the event of thromboembolic events with revascularization, transsphenoidal surgery, and the surveillance and detection of associated cerebral aneurysms. We report a case of a 25-year-old man who presented with headache since 2 years ago, and was incidentally discovered to have a congenital bilateral absence of ICAs.

4.
Investigative Magnetic Resonance Imaging ; : 71-74, 2016.
Artículo en Inglés | WPRIM | ID: wpr-223255

RESUMEN

Wernicke's encephalopathy (WE) is an acute neurological disorder resulting from thiamine deficiency. Early diagnosis and treatment of WE is important to avoid persistent brain damage. Although histopathologic examination usually demonstrates pin-point hemorrhages in affected brain parenchyma, secondary hemorrhage is a rare but serious complication of WE. We experienced a rare case of intracranial hemorrhage related to WE in a 56-year-old male patient with malnourishment.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Encéfalo , Diagnóstico Precoz , Hemorragia , Hemorragias Intracraneales , Imagen por Resonancia Magnética , Enfermedades del Sistema Nervioso , Deficiencia de Tiamina , Encefalopatía de Wernicke
5.
Journal of the Korean Society of Magnetic Resonance in Medicine ; : 290-302, 2014.
Artículo en Inglés | WPRIM | ID: wpr-77851

RESUMEN

PURPOSE: Susceptibility-weighted magnetic resonance (MR) sequence is three-dimensional (3D), spoiled gradient-echo pulse sequences that provide a high sensitivity for the detection of blood degradation products, calcifications, and iron deposits. This pictorial review is aimed at illustrating and discussing its main clinical applications. MATERIALS AND METHODS: SWI is based on high-resolution, 3D, fully velocity-compensated gradient-echo sequences using both magnitude and phase images. To enhance the visibility of the venous structures, the magnitude images are multiplied with a phase mask generated from the filtered phase data, which are displayed at best after post-processing of the 3D dataset with the minimal intensity projection algorithm. A total of 200 patients underwent MR examinations that included SWI on a 3 tesla MR imager were enrolled. RESULTS: SWI is very useful in detecting multiple brain disorders. Among the 200 patients, 80 showed developmental venous anomaly, 22 showed cavernous malformation, 12 showed calcifications in various conditions, 21 showed cerebrovascular accident with susceptibility vessel sign or microbleeds, 52 showed brain tumors, 2 showed diffuse axonal injury, 3 showed arteriovenous malformation, 5 showed dural arteriovenous fistula, 1 showed moyamoya disease, and 2 showed Parkinson's disease. CONCLUSION: SWI is useful in detecting occult low flow vascular lesions, calcification and microbleed and characterising diverse brain disorders.


Asunto(s)
Humanos , Malformaciones Arteriovenosas , Encéfalo , Encefalopatías , Neoplasias Encefálicas , Malformaciones Vasculares del Sistema Nervioso Central , Conjunto de Datos , Lesión Axonal Difusa , Hierro , Imagen por Resonancia Magnética , Máscaras , Enfermedad de Moyamoya , Neuroimagen , Enfermedad de Parkinson , Accidente Cerebrovascular
6.
Korean Journal of Radiology ; : S30-S33, 2008.
Artículo en Inglés | WPRIM | ID: wpr-65665

RESUMEN

Cholesterol granuloma (CG) is usually associated with chronic middle ear disease, and is not common in the paranasal sinuses. Additionally, it is very rare for cases of CG to be associated with a fungal infection. However, in this paper, we report a case of sphenoid sinus CG that is associated with aspergilloma in a 78-year-old male patient who presented with right hemifacial pain, headache and toothache. CT revealed the presence of an expansile cystic mass lesion in the sphenoid sinus that showed a high signal intensity on both the T1 and T2 weighted images. This mass was later determined to be CG. The suspected etiologic mechanisms of both CG and aspergilloma of the paranasal sinuses are similar, and impaired drainage and obstruction of the ventilation of the paranasal sinuses are considered to be the causative mechanism of both diseases. Overall, the results of this study indicate that the use of MRI findings could be helpful for differentiating CG from other paranasal sinus mass lesions.


Asunto(s)
Anciano , Humanos , Masculino , Aspergilosis/complicaciones , Granuloma/diagnóstico , Imagen por Resonancia Magnética , Enfermedades de los Senos Paranasales/complicaciones , Seno Esfenoidal , Tomografía Computarizada por Rayos X
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA