AI Article Synopsis
- Early detection and treatment of total anomalous pulmonary venous connection (TAPVC) are crucial for improving outcomes, as showcased by a 7-month-old patient diagnosed after experiencing cyanotic episodes.
- TAPVC is a rare congenital heart defect characterized by abnormal blood flow, with the infracardiac subtype presenting a risk of obstruction and often diagnosed in newborns.
- Successful surgical intervention and a stable recovery in this case highlight the need for thorough newborn exams and timely referrals to specialists to address this serious condition effectively.
Article Abstract
Key Clinical Message: This case underscores the importance of early detection and treatment for total anomalous pulmonary venous connection, a rare congenital heart condition, through comprehensive newborn physical exams and prompt specialist referrals.
Abstract: Total anomalous pulmonary venous connection (TAPVC) is a rare form of congenital heart disease that is typically diagnosed in neonates. TAPVC has four subtypes, with the infracardiac type at risk of obstruction. TAPVC is usually diagnosed in newborns but can occur in other age groups. In this case, a 7-month-old male with recurrent cyanotic episodes was diagnosed with TAPVC of the infracardiac type using computed tomography angiography. The patient underwent successful surgical repair with a favorable postoperative course and was discharged in stable condition, and further follow-up was not possible beyond 2 months. This case emphasizes the importance of early recognition and management of this condition to prevent the progression of subsequent complications.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580688 | PMC |
| http://dx.doi.org/10.1002/ccr3.8079 | DOI Listing |
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