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1.
J Ultrasound Med ; 36(5): 869-878, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28230264

RESUMO

A ventricular septal defect is the most common congenital cardiac abnormality encountered in infants and children. Many of them survive through adulthood before diagnosis. Two-thirds of the cases involve the membranous part of the septum. In the absence of an interventricular shunt or concomitant cardiac surgery, guidelines for surgical intervention or resection of isolated aneurysms of the membranous septum are not well established. In this report, we discuss a multi-imaging modality approach for the diagnosis and assessment of membranous ventricular septal aneurysms and review the experts' consensuses for follow-up and treatment strategies.


Assuntos
Ecocardiografia/métodos , Aneurisma Cardíaco/diagnóstico por imagem , Comunicação Interventricular/diagnóstico por imagem , Tomografia Computadorizada por Raios X/métodos , Septo Interventricular/diagnóstico por imagem , Idoso , Humanos , Masculino , Pessoa de Meia-Idade
2.
J Cardiol Cases ; 7(6): e173-e175, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30533156

RESUMO

Syncope is defined as a transient loss of consciousness due to cerebral hypoperfusion characterized by rapid onset, short duration, and spontaneous complete recovery. Numerous causes of syncope have been described. Vasovagal syncope is the most common with a number of precipitants. We report a case of post herpetic trigeminal neuralgia leading to neurocardiogenic syncope. These episodes were preceded by severe stabbing left frontal headaches followed by significant sinus bradycardia, asystole, and syncope requiring pacemaker implantation. To our knowledge only one previous case of post herpetic trigeminal neuralgia leading to syncope has been reported. .

4.
J Invasive Cardiol ; 22(8): E159-61, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20679684

RESUMO

We report a case of a complicated vascular access secondary to systemic venous defects which have not been previously reported. Further evaluation revealed congenital absence of superior vena cava with two brachiocephalic veins draining separately. He also had absence of the hepatic segment of the inferior vena cava with azygos continuation. The patient did not have congenital anomalies of the remaining thoracoabdominal vasculature and viscera.


Assuntos
Veia Ázigos/anormalidades , Veia Cava Inferior/anormalidades , Veia Cava Superior/anormalidades , Síndrome de Wolff-Parkinson-White/patologia , Veia Ázigos/diagnóstico por imagem , Veias Braquiocefálicas/anormalidades , Veias Braquiocefálicas/diagnóstico por imagem , Cateterismo Cardíaco , Humanos , Masculino , Pessoa de Meia-Idade , Flebografia , Tomografia Computadorizada por Raios X , Veia Cava Inferior/diagnóstico por imagem , Veia Cava Superior/diagnóstico por imagem
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