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Isolated absence of right pulmonary artery in a 4-year old child: a case report
Abate Yeshidinber Weldetsadik1, Yemisrach Mekonnen Asfaw1, Atnafu Mekonnen Tekleab1
1Department of Pediatrics and Child Health, Saint Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia, atnemekonnen@yahoo.com.
Insights
Isolated absence of the pulmonary artery is a rare congenital condition. This case highlights a 4-year-old with isolated absence of the right pulmonary artery presenting with recurrent respiratory issues.
Area of Science:
- Cardiology
- Pediatric Pulmonology
- Congenital Anomalies
Background:
- Isolated unilateral absence of the pulmonary artery (IUAPA) is a rare congenital heart defect.
- Typically diagnosed in adolescence, IUAPA involves the absence of one pulmonary artery without other cardiac malformations.
Observation:
- A 4-year-old male presented with recurrent chest infections and wheezing since infancy.
- The patient exhibited symptoms suggestive of a pulmonary issue despite his young age.
Findings:
- The case involved isolated absence of the right pulmonary artery.
- This diagnosis in a young child is unusual, as it's often detected later in life.
Implications:
- Early diagnosis of IUAPA can be challenging, especially in pediatric patients.
- Recurrent respiratory infections may be an indicator of this rare anomaly in children.
- Further research into pediatric presentations of IUAPA is warranted.
Abstract:
Isolated unilateral absence of the pulmonary artery is a rare anomaly with congenital absence of the left or right pulmonary artery in the absence of other cardiac malformation, and diagnosis is usually made during adolescence. We report a 4-year old male child with isolated absence of the right pulmonary artery, who presented with recurrent chest infection and wheezing since infancy.
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Types of Reports I: Hands-off Report
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