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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Se presenta el caso de un reci&#233;n nacido con isomerismo auricular derecho&#44; cardiopat&#237;a cong&#233;nita compleja y conexi&#243;n venosa pulmonar an&#243;mala total doble asociada que hab&#237;a sido diagnosticado fiablemente con ecocardiograf&#237;a Doppler bidimensional en color&#46; Seguimiento clinic en un neonato tratado con prostaglandina desde las 24 h de vida hasta su deceso postoperatorio&#46; La cianosis y el soplo card&#237;aco que evolucion&#243; a distr&#233;s respiratorio conforman el marco cl&#237;nico de un reci&#233;n nacido var&#243;n sin antecedentes obst&#233;tricos relevantes&#46; La ecocardiograf&#237;a emostr&#243; situs indeterminado&#44; hipoplasia severa de ventr&#237;culo izquierdo&#44; atresia pulmonar y conducto arterioso permeable&#46; Las venas pulmonares se reun&#237;an en un collector posterior a la aur&#237;cula &#250;nica&#44; del que ascend&#237;a una vena emisaria vertical que conecta con un saco aneurism&#225;tico&#46; De &#233;ste emergen dos vasos venosos&#58; uno hacia vena innominada y otro que conectaba con el techo auricular&#46; El cateterismo card&#237;aco confirm&#243; la malformaci&#243;n y el enfermo es remitido a cirug&#237;a al sexto d&#237;a de vida&#44; realiz&#225;ndose anastomosis del colector venoso a la aur&#237;cula &#250;nica&#44; implante de una f&#237;stula tipo Blalock-Taussig modificada y el cierre del conducto arterioso&#59; el enfermo falleci&#243; en la sala operatoria&#46; La asociaci&#243;n de malformaci&#243;n compleja intracard&#237;aca y conexi&#243;n venosa pulmonar an&#243;mala total obstructiva en el contexto de heterotaxia visceroauricular derecha es letal y pocos son los supervivientes con cirug&#237;a correctora neonatal&#46; La ecocardiograf&#237;a Doppler en color es fiable para el diagn&#243;stico y supone una gu&#237;a indispensable para dirigir el estudio angiogr&#225;fico&#46;</p>"
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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">W e present a newborn infant with right atrial isomerism&#44; complex congenital heart malformation and anomalous pulmonary venous connection&#44; reliably diagnosed by 2-D Doppler color echocardiography&#46; The infant had no significant obstetric antecedents&#46; The neonatal clinical picture included cyanosis&#44; heart murmur and respiratory distress&#46; The infant was treated with prostaglandin fro m the age of 24 hours until his death after surgery&#46; The 2-D echo Doppler color flow mapping showed findings that suggested right atrial isomerism&#44; severe left ventricular hypoplasia&#44; pulmonary atresia and ductus arteriosus&#46; The pulmonary veins flowed together to a posterior cardiac chamber from which an emissary vertical venous vessel connected with a left superior aneurysmal sack&#46; Two venous channels emerged from this sack&#58; one connecting to the innominate vein and the other to the atrium&#46; The malformations were confirmed by cardiac catheterization&#46; On the sixth day of life&#44; the patient underwent anastomosis between the posterior venous chamber with the atrium&#44; a modified Blalock-Taussig shunt implant&#44; and ductus closure but died during surgery&#46; The association between complex cardiac anomalies and uncommon obstructive total anomalous pulmonary venous connection in the context of right atrial isomerism is lethal and few neonates survive surgical repair&#46;Tw o-dimensional echo color flow Doppler is a reliable diagnostic technique and an indispensable guide in angiography&#46;</p>"
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Conexión venosa pulmonar anómala total doble
Double total anomalous pulmonary venous connection
S. Matiza, R. Tamariz-Martela, M. Cazzanigaa,
Autor para correspondencia
marcazza@inicia.es

Correspondencia: Servicio Cardiología Pediátrica. Hospital Ramón y Cajal.Ctra. Colmenar Viejo, km 9,100. 28034 Madrid.
, J.L. Vázquez Martínezb, F. Villagrá Blancoc
a Servicio de Cardiología Pediátrica. Hospital Ramón y Cajal. Madrid.
b Unidad de Cuidados Intensivos Pediátricos y Cardiovasculares. Hospital Ramón y Cajal. Madrid.
c Cirugía Cardiovascular Infantil. Hospital Ramón y Cajal. Madrid.
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Se presenta el caso de un reci&#233;n nacido con isomerismo auricular derecho&#44; cardiopat&#237;a cong&#233;nita compleja y conexi&#243;n venosa pulmonar an&#243;mala total doble asociada que hab&#237;a sido diagnosticado fiablemente con ecocardiograf&#237;a Doppler bidimensional en color&#46; Seguimiento clinic en un neonato tratado con prostaglandina desde las 24 h de vida hasta su deceso postoperatorio&#46; La cianosis y el soplo card&#237;aco que evolucion&#243; a distr&#233;s respiratorio conforman el marco cl&#237;nico de un reci&#233;n nacido var&#243;n sin antecedentes obst&#233;tricos relevantes&#46; La ecocardiograf&#237;a emostr&#243; situs indeterminado&#44; hipoplasia severa de ventr&#237;culo izquierdo&#44; atresia pulmonar y conducto arterioso permeable&#46; Las venas pulmonares se reun&#237;an en un collector posterior a la aur&#237;cula &#250;nica&#44; del que ascend&#237;a una vena emisaria vertical que conecta con un saco aneurism&#225;tico&#46; De &#233;ste emergen dos vasos venosos&#58; uno hacia vena innominada y otro que conectaba con el techo auricular&#46; El cateterismo card&#237;aco confirm&#243; la malformaci&#243;n y el enfermo es remitido a cirug&#237;a al sexto d&#237;a de vida&#44; realiz&#225;ndose anastomosis del colector venoso a la aur&#237;cula &#250;nica&#44; implante de una f&#237;stula tipo Blalock-Taussig modificada y el cierre del conducto arterioso&#59; el enfermo falleci&#243; en la sala operatoria&#46; La asociaci&#243;n de malformaci&#243;n compleja intracard&#237;aca y conexi&#243;n venosa pulmonar an&#243;mala total obstructiva en el contexto de heterotaxia visceroauricular derecha es letal y pocos son los supervivientes con cirug&#237;a correctora neonatal&#46; La ecocardiograf&#237;a Doppler en color es fiable para el diagn&#243;stico y supone una gu&#237;a indispensable para dirigir el estudio angiogr&#225;fico&#46;</p>"
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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">W e present a newborn infant with right atrial isomerism&#44; complex congenital heart malformation and anomalous pulmonary venous connection&#44; reliably diagnosed by 2-D Doppler color echocardiography&#46; The infant had no significant obstetric antecedents&#46; The neonatal clinical picture included cyanosis&#44; heart murmur and respiratory distress&#46; The infant was treated with prostaglandin fro m the age of 24 hours until his death after surgery&#46; The 2-D echo Doppler color flow mapping showed findings that suggested right atrial isomerism&#44; severe left ventricular hypoplasia&#44; pulmonary atresia and ductus arteriosus&#46; The pulmonary veins flowed together to a posterior cardiac chamber from which an emissary vertical venous vessel connected with a left superior aneurysmal sack&#46; Two venous channels emerged from this sack&#58; one connecting to the innominate vein and the other to the atrium&#46; The malformations were confirmed by cardiac catheterization&#46; On the sixth day of life&#44; the patient underwent anastomosis between the posterior venous chamber with the atrium&#44; a modified Blalock-Taussig shunt implant&#44; and ductus closure but died during surgery&#46; The association between complex cardiac anomalies and uncommon obstructive total anomalous pulmonary venous connection in the context of right atrial isomerism is lethal and few neonates survive surgical repair&#46;Tw o-dimensional echo color flow Doppler is a reliable diagnostic technique and an indispensable guide in angiography&#46;</p>"
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ISSN: 16954033
Idioma original: Español
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