Percutaneous closure of congenital aortocaval fistula with a coexisting secundum atrial septal defect

Poay Huan Loh; Tim Jensen; Lars Søndergaard

doi:10.1017/s1047951111002046

Percutaneous closure of congenital aortocaval fistula with a coexisting secundum atrial septal defect

Poay Huan Loh, Tim Jensen, Lars Søndergaard

4 Citationer (Scopus)

Abstract

Congenital aortocaval fistula is a very rare anomaly. Clinically, it resembles conditions that cause left-to-right shunt of blood. We report a case of such anomaly in combination with a secundum atrial septal defect in a 13-month-old girl who presented with failure to thrive and exertional respiratory symptoms. The aortocaval fistula was occluded percutaneously using an Amplatzer® Duct Occluder.

Originalsprog	Engelsk
Tidsskrift	Cardiology in the Young
Vol/bind	22
Udgave nummer	4
Sider (fra-til)	472-474
Antal sider	3
ISSN	1047-9511
DOI	https://doi.org/10.1017/s1047951111002046
Status	Udgivet - aug. 2012

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10.1017/s1047951111002046

Citationsformater

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title = "Percutaneous closure of congenital aortocaval fistula with a coexisting secundum atrial septal defect",

abstract = "Congenital aortocaval fistula is a very rare anomaly. Clinically, it resembles conditions that cause left-to-right shunt of blood. We report a case of such anomaly in combination with a secundum atrial septal defect in a 13-month-old girl who presented with failure to thrive and exertional respiratory symptoms. The aortocaval fistula was occluded percutaneously using an Amplatzer{\textregistered} Duct Occluder.",

author = "Loh, {Poay Huan} and Tim Jensen and Lars S{\o}ndergaard",

year = "2012",

month = aug,

doi = "10.1017/s1047951111002046",

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volume = "22",

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issn = "1047-9511",

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T1 - Percutaneous closure of congenital aortocaval fistula with a coexisting secundum atrial septal defect

AU - Loh, Poay Huan

AU - Jensen, Tim

AU - Søndergaard, Lars

PY - 2012/8

Y1 - 2012/8

N2 - Congenital aortocaval fistula is a very rare anomaly. Clinically, it resembles conditions that cause left-to-right shunt of blood. We report a case of such anomaly in combination with a secundum atrial septal defect in a 13-month-old girl who presented with failure to thrive and exertional respiratory symptoms. The aortocaval fistula was occluded percutaneously using an Amplatzer® Duct Occluder.

AB - Congenital aortocaval fistula is a very rare anomaly. Clinically, it resembles conditions that cause left-to-right shunt of blood. We report a case of such anomaly in combination with a secundum atrial septal defect in a 13-month-old girl who presented with failure to thrive and exertional respiratory symptoms. The aortocaval fistula was occluded percutaneously using an Amplatzer® Duct Occluder.

U2 - 10.1017/s1047951111002046

DO - 10.1017/s1047951111002046

M3 - Journal article

C2 - 22182401

SN - 1047-9511

VL - 22

SP - 472

EP - 474

JO - Cardiology in the Young

JF - Cardiology in the Young

IS - 4

ER -

Percutaneous closure of congenital aortocaval fistula with a coexisting secundum atrial septal defect

Abstract

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