A 30-year-old male with tetralogy of Fallot presented with a history of hemoptysis. He had a major aortopulmonary collateral artery that could not be interrupted during corrective surgery due to technical problems. Postoperative recovery was complicated by congestive heart failure. Embolization of the aortopulmonary collateral artery was planned but he developed massive hemoptysis and emergency transcatheter occlusion was performed, which successfully controlled both hemoptysis and congestive heart failure.
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References
1.
HaroutunianLMNeillCA. Pulmonary complications of congenital heart disease: hemoptysis. Am Heart J1972; 84: 540–59.
2.
SzarnickiRKrebberHJWackJ. Wire coil embolization of systemic pulmonary artery collaterals following surgical correction of pulmonary atresia. J Thorac Cardiovasc Surg1981; 82: 124–6.
3.
ZuberbuhlerJRDanknerEZoltunRBurkholderJBahnsonHT. Tissue adhesive closure of aortic pulmonary communications. Am Heart J1974; 88: 41–6.
4.
GrinnellVSMehringerCMHieshimaGBStanleyPLuriePR. Transaortic occlusion of collateral arteries to the lung by detachable valved balloons in a patient with tetralogy of Fallot. Circulation1982; 65: 1276–8.
5.
YamamotoSNozawaTAizawaTHondaMMohriM. Transcatheter embolization of bronchial collateral arteries prior to intracardiac operation for tetralogy of Fallot. J Thorac Cardiovasc Surg1979; 78: 739–43.
6.
McGoonDCBairdDKDavisGD. Surgical management of large bronchial collateral arteries with pulmonary stenosis or atresia. Circulation1975; 52: 109–18.
7.
KaufmanSLKanSJMitchellSEFlahertyJTWhiteRI. Embolization of systemic to pulmonary artery collaterals in the management of hemoptysis in pulmonary atresia. Am J Cardiol1986; 58: 1130–2.