Rebuttal: aortic coarctation and concomitant anomalies - left circumflex fistula, persistent left SVC and ventricular

Abrar Alameri1, Ahmed Sherif2

  • 1Imaging Insititute, Cleveland Clinic Abu Dhabi, Abu Dhabi, Abu Dhabi, UAE.

BMJ Case Reports
|February 24, 2026
PubMed

Insights

Coarctation of the aorta (COA) is a common congenital heart defect. This case highlights a rare combination of COA with multiple cardiovascular anomalies, emphasizing the complexity of managing such conditions.

Area of Science:

  • Cardiology
  • Congenital Heart Disease
  • Medical Case Reports

Background:

  • Coarctation of the aorta (COA) is a significant congenital cardiovascular anomaly affecting up to 6 per 1000 live births.
  • Associated rare cardiovascular anomalies can complicate COA management.
  • Hypertension in adolescents can be an indicator of underlying COA.

Purpose of the Study:

  • To report a rare case of coarctation of the aorta in an adolescent male.
  • To describe the incidental diagnosis of hypertension leading to COA detection.
  • To document an unprecedented association of COA with specific rare anomalies.

Main Methods:

  • Case presentation of an adolescent male with incidental hypertension.
  • Diagnostic imaging to confirm coarctation of the aorta.
  • Literature review to assess the novelty of associated anomalies.

Main Results:

  • Coarctation of the aorta was confirmed via imaging.
  • The patient presented with multiple, rarely associated cardiovascular anomalies.
  • The specific combination of COA with left circumflex to coronary sinus fistula, ventricular diverticulum, and persistent left superior vena cava appears to be previously unreported.

Conclusions:

  • This case underscores the importance of investigating hypertension in adolescents.
  • The co-occurrence of COA with these specific anomalies presents a unique clinical scenario.
  • Further research may be needed to understand the implications of such complex congenital heart defect associations.

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