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CASE REPORT
Year : 2021  |  Volume : 7  |  Issue : 1  |  Page : 60-62

An unusual case report of two cases with coexisting type I aortopulmonary window with tetralogy of fallot with pulmonary atresia


Department of Cardiothoracic and Vascular Surgery, Cardiothoracic and Neurosciences Centre, All India Institute of Medical Sciences, New Delhi, India

Correspondence Address:
Palleti Rajashekar
Department of Cardiothoracic and Vascular Surgery, Cardiothoracic and Neurosciences Centre, CTVS Office, 7th Floor, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110 029
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jpcs.jpcs_92_20

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Aortopulmonary window is an uncommon truncal anomaly. Its coexistence with tetralogy of Fallot (TOF) with pulmonary atresia is rare. This rare complex association is always a surgical challenge due to lack of an established surgical approach. The association with TOF makes the interventional approach unlikely. In the two cases summarized below, we have addressed the investigation strategy reaching the final diagnosis. The surgical interventions and our decision-making in the final adopted technique have been highlighted. The relevant surgical outcome with postoperative follow-up has been discussed. The rarity of this association without a standard management algorithm mandates the relevance of this presentation.


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