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1.
Interv Neuroradiol ; 18(2): 153-7, 2012 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-22681729

RESUMEN

The clinical implications of venous cerebrovascular maldevelopment remain poorly understood. We report on the association of cerebrofacial venous anomalies (including sinus pericranii), ocular abnormalities and mild developmental delay in two children. In addition, one child had a seizure disorder. Complex cerebrofacial slow-flow vascular anomalies may herald an underlying developmental aberration affecting the cerebrofacial and orbital regions.


Asunto(s)
Malformaciones Arteriovenosas/complicaciones , Discapacidades del Desarrollo/complicaciones , Anomalías del Ojo/complicaciones , Seno Pericraneal/complicaciones , Malformaciones Arteriovenosas/diagnóstico , Angiografía Cerebral , Niño , Preescolar , Discapacidades del Desarrollo/diagnóstico , Anomalías del Ojo/diagnóstico , Humanos , Imagen por Resonancia Magnética , Masculino , Seno Pericraneal/diagnóstico , Tomografía Computarizada por Rayos X
2.
Phlebology ; 27(5): 242-4, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22106447

RESUMEN

The use of a simplified system for perivenous infusion of tumescent fluid prior to endovenous laser ablation is described. Two infusion bag systems using different combinations of needle sizes (22, 23 and 25 gauge) and pressure settings (300 and 600 mmHg) as well as hand injections were tested in vivo. The technique is simple, safe and may lead to quicker infusion, reduction in hand fatigue and reduced cost.


Asunto(s)
Terapia por Láser/métodos , Várices/cirugía , Adolescente , Adulto , Niño , Femenino , Humanos , Terapia por Láser/efectos adversos , Masculino
3.
Phys Med Biol ; 56(7): 2183-97, 2011 Apr 07.
Artículo en Inglés | MEDLINE | ID: mdl-21403185

RESUMEN

Contrast-enhanced ultrasound (US) imaging is potentially applicable to the clinical investigation of a wide variety of perfusion disorders. Quantitative analysis of perfusion is not widely performed, and is limited by the fact that data are acquired from a single tissue plane, a situation that is unlikely to accurately reflect global perfusion. Real-time perfusion information from a tissue volume in an experimental rabbit model of testicular torsion was obtained with a two-dimensional matrix phased array US transducer. Contrast-enhanced imaging was performed in 20 rabbits during intravenous infusion of the microbubble contrast agent Definity® before and after unilateral testicular torsion and contralateral orchiopexy. The degree of torsion was 0° in 4 (sham surgery), 180° in 4, 360° in 4, 540° in 4, and 720° in 4. An automated technique was developed to analyze the time history of US image intensity in experimental and control testes. Comparison of mean US intensity rate of change and of ratios between mean US intensity rate of change in experimental and control testes demonstrated good correlation with testicular perfusion and mean perfusion ratios obtained with radiolabeled microspheres, an accepted 'gold standard'. This method is of potential utility in the clinical evaluation of testicular and other organ perfusion.


Asunto(s)
Circulación Sanguínea , Medios de Contraste , Torsión del Cordón Espermático/diagnóstico por imagen , Torsión del Cordón Espermático/fisiopatología , Animales , Modelos Animales de Enfermedad , Masculino , Conejos , Torsión del Cordón Espermático/patología , Factores de Tiempo , Ultrasonografía
4.
AJNR Am J Neuroradiol ; 32(10): 1812-7, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21310861

RESUMEN

CLOVES syndrome is a complex disorder of congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and skeletal/scoliosis/spinal anomalies. We report the occurrence of spinal-paraspinal fast-flow lesions within or adjacent to the truncal overgrowth or a cutaneous birthmark in 6 patients with CLOVES syndrome.


Asunto(s)
Anomalías Múltiples/patología , Malformaciones Arteriovenosas/patología , Imagen por Resonancia Magnética , Médula Espinal/anomalías , Médula Espinal/patología , Columna Vertebral/anomalías , Columna Vertebral/patología , Adolescente , Preescolar , Femenino , Humanos , Masculino , Síndrome
5.
Clin Genet ; 78(4): 342-7, 2010 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-21050185

RESUMEN

CLOVES syndrome is a recently described overgrowth disorder with complex vascular anomalies. Careful analysis of the case report by the German physician Hermann Friedberg "gigantism of the right lower limb" published in 1867 revealed that the report probably represents one of the first written accounts of CLOVES syndrome.


Asunto(s)
Gigantismo/historia , Anomalías Musculoesqueléticas/historia , Malformaciones Vasculares/historia , Anomalías Múltiples/historia , Desarrollo Óseo , Femenino , Deformidades Congénitas del Pie/historia , Alemania , Deformidades Congénitas de la Mano/historia , Historia del Siglo XIX , Humanos , Escoliosis/historia , Telangiectasia/historia
6.
AJNR Am J Neuroradiol ; 31(9): 1608-12, 2010 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-20651014

RESUMEN

BACKGROUND AND PURPOSE: KTS is a rare limb overgrowth disorder with slow-flow vascular anomalies. This study examines the presumed association between KTS and spinal AVMs. MATERIALS AND METHODS: We performed a MEDLINE search of articles and reviewed textbooks of spinal diseases to study the association between KTS and spinal AVM. Our goal was to ascertain the basis on which the diagnosis of KTS was established and to evaluate the evidence of its association with spinal AVMs. In addition, the data base of the Vascular Anomalies Center at Children's Hospital Boston was queried for patients with KTS, and the association with spinal AVM was investigated. RESULTS: Twenty-four published reports on spinal AVMs in 31 patients with KTS were reviewed. None of these references provided solid evidence of the diagnosis of KTS in any patient. Clinical data were either incompatible with the diagnosis of KTS or were inadequate to establish the diagnosis. Alternative possible diagnoses (CLOVES syndrome and CM-AVM) were suggested by the first author for 9 of the patients reported in these articles. The medical records of 208 patients with the diagnosis of KTS were analyzed; not a single patient had clinical or radiologic evidence of a spinal AVM. CONCLUSIONS: An association between KTS and spinal AVM, as posited in numerous references, is most likely erroneous. The association has neither been reliably proved in the limited published literature nor encountered in a large cohort.


Asunto(s)
Malformaciones Arteriovenosas/diagnóstico por imagen , Malformaciones Arteriovenosas/epidemiología , Síndrome de Klippel-Trenaunay-Weber/diagnóstico por imagen , Síndrome de Klippel-Trenaunay-Weber/epidemiología , Médula Espinal/anomalías , Médula Espinal/irrigación sanguínea , Niño , Preescolar , Comorbilidad , Femenino , Humanos , Incidencia , Recién Nacido , Masculino , Radiografía , Medición de Riesgo , Factores de Riesgo
8.
AJNR Am J Neuroradiol ; 30(6): 1273-4, 2009 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19246525

RESUMEN

This brief case report describes an unusual presumed association of chronic HIV infection with multiple cerebral arteriovenous malformations. An adult male patient presented with recurrent spontaneous brain intracranial hemorrhages and neurologic deficits requiring surgical evacuation. The diagnosis was delayed because of lack of a high index of suspicion of this unexpected and previously unrecognized association.


Asunto(s)
Anomalías Múltiples/diagnóstico , Angiografía Cerebral , Infecciones por VIH/complicaciones , Infecciones por VIH/diagnóstico , Malformaciones Arteriovenosas Intracraneales/complicaciones , Malformaciones Arteriovenosas Intracraneales/diagnóstico , Angiografía por Resonancia Magnética , Humanos , Masculino , Persona de Mediana Edad
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