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1.
World J Pediatr Congenit Heart Surg ; 7(2): 234-7, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26655350

RESUMO

Multiple saccular aneurysms of the thoracic aorta in neonates and infants are exceedingly rare. An association of these aneurysms with Loeys-Dietz syndrome (LDS) in older age-groups is well known. This case report describes the diagnosis and subsequent successful repair of aortic coarctation associated with double saccular aneurysms of the thoracic aorta in patient with LDS during the first year of life.


Assuntos
Aneurisma da Aorta Torácica/diagnóstico , Coartação Aórtica/diagnóstico , Síndrome de Loeys-Dietz , Angiografia , Aneurisma da Aorta Torácica/cirurgia , Coartação Aórtica/cirurgia , Diagnóstico Precoce , Intervenção Médica Precoce , Humanos , Imageamento Tridimensional , Lactente , Masculino , Diagnóstico Pré-Natal , Tomografia Computadorizada por Raios X
2.
Ann Thorac Surg ; 83(2): 613-8, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17257996

RESUMO

BACKGROUND: Tetralogy of Fallot with unilateral absence of the pulmonary artery is a rare congenital heart defect that still represents a surgical challenge. The purpose of this study is to summarize our experience of surgical treatment of this complex lesion. METHODS: From 1983 to 2003, 27 patients with tetralogy of Fallot and unilateral absence of the left (n = 25) or right (n = 2) pulmonary artery underwent different surgical interventions. The age of patients ranged from 40 days to 37 years (median, 5.3 years). Pulmonary arterial Nakata index and Nakata index Z-score were used for the quantitative assessment of the contralateral pulmonary artery. Twenty patients underwent various palliative procedures, namely Blalock-Taussig or Gore-Tex shunt, transluminal balloon pulmonary valvuloplasty, and reconstruction of right ventricular outflow tract without ventricular septal defect closure. At a median interval of 3.6 years after palliation, 13 patients underwent complete repair of tetralogy of Fallot. In the other 7 patients, complete repair was performed as a primary intervention. RESULTS: Hospital mortality after palliation and after a complete repair was the same and reached 5%. Sixteen patients with the Nakata index greater than 200 mm2/m2 and Z-score greater than -4 survived after a complete repair. One of 4 patients with Nakata index less than 200 mm2/m2 and Z-score less than -4 died after surgery. CONCLUSIONS: Majority of patients with tetralogy of Fallot and unilateral absence of the pulmonary artery require palliative intervention as a first step of surgical treatment. Nakata index greater than 200 mm2/m2 and Nakata index Z-score greater than -4 are criteria for a successful complete repair.


Assuntos
Procedimentos Cirúrgicos Cardiovasculares , Artéria Pulmonar/anormalidades , Tetralogia de Fallot/cirurgia , Adolescente , Adulto , Procedimentos Cirúrgicos Cardiovasculares/mortalidade , Criança , Pré-Escolar , Anormalidades Congênitas/fisiopatologia , Feminino , Mortalidade Hospitalar , Humanos , Lactente , Masculino , Cuidados Paliativos , Índice de Gravidade de Doença , Análise de Sobrevida
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