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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Pulmonary sequestration is a rare disease consisting of a non-functioning bronchopulmonary mass separated from the tracheobronchial tree&#44; supplied from a systemic artery&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 20-year-old primigravida was referred to the fetal cardiology clinic at 22 weeks&#8217; gestation due to an intrapulmonary mass suggestive of pulmonary sequestration&#46; The fetal echocardiogram showed a structurally normal heart and a tortuous feeding vessel arising from the abdominal aorta&#44; proximally to the celiac trunk &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41;&#46; She maintained regular follow-up&#44; during which time the intrapulmonary mass gradually decreased in size and the collateral artery disappeared&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">A 1&#46;5-month-old infant was referred for a paediatric cardiology review due to poor weight gain and breathlessness&#46; On examination&#44; he had increased work of breathing and a gallop rhythm&#46; The transthoracic echocardiogram showed dilatation of the left atrium and ventricle&#44; and no intracardiac shunts&#46; Chest computed tomography showed a large aortopulmonary collateral artery originating in the abdominal aorta &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#44; irrigating a small portion of the right lower lobe&#46; He underwent transcatheter embolization of the collateral artery &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a>&#41; and is now 12 months old and asymptomatic&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">These are two cases of pulmonary sequestration with different presentations&#44; outcomes and treatment&#46; In the first case&#44; the diagnosis was made antenatally and the feeding vessel disappeared spontaneously&#46; The second case initially presented with heart failure and required interventional closure of the aortopulmonary collateral&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Most pulmonary sequestrations regress spontaneously in utero&#46; When this does not occur&#44; the child may develop symptoms and transcatheter embolization can be a successful alternative to surgery in selected cases&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of interest</span><p id="par0030" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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