Unique Prenatal Diagnosis of a Coronary Sinus Aneurysm

BACKGROUND: Congenital cardiac aneurysms are very rare in pediatric and fetal populations and can compose a range of anomalies, including ventricular, atrial, and coronary sinus aneurysm. Accurate recognition is essential because embryologic origins, imaging features, and clinical implications significantly differ. CASE SUMMARY: A 16-year-old primigravida young woman was evaluated at 23 5/7 weeks' gestation in the fetal cardiology clinic for evaluation of a suspected thoracic cyst. Fetal echocardiography and magnetic resonance imaging demonstrated a large aneurysm arising from dilated coronary sinus with impressive posterior and inferior extension without persistent left superior vena cava. No hydrops, arrhythmia, or pericardial effusion were present. Postnatal echocardiography and computed tomography angiography confirmed a rare presentation of a coronary sinus aneurysm. DISCUSSION: Coronary sinus aneurysms arise from abnormal venous wall development or hemodynamic stress and must be distinguished from ventricular or atrial outpouchings, which carry variable risks of rupture, arrhythmia, or hydrops. Early fetal diagnosis permits accurate classification, anticipatory counseling, and tailored postnatal management. TAKE-HOME MESSAGES: This case illustrates the importance of distinguishing coronary sinus aneurysm from ventricular or atrial aneurysms. Prenatal recognition facilitates accurate diagnosis, risk assessment, counseling, and delivery planning.

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Publication Details

Journal
JACC Case Reports
Published
2026-04-01
DOI
https://doi.org/10.1016/j.jaccas.2026.107822
Primary Topic
Kawasaki Disease and Coronary Complications
Type
article
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article

Unique Prenatal Diagnosis of a Coronary Sinus Aneurysm

Christopher Lindblade, Michael Nguyen, Zareh Torabyan, Ryan Johnson
JACC Case Reports
Kawasaki Disease and Coronary Complications
article

Unique Prenatal Diagnosis of a Coronary Sinus Aneurysm

Christopher Lindblade, Michael Nguyen, Zareh Torabyan, Ryan Johnson
article en

Abstract

BACKGROUND: Congenital cardiac aneurysms are very rare in pediatric and fetal populations and can compose a range of anomalies, including ventricular, atrial, and coronary sinus aneurysm. Accurate recognition is essential because embryologic origins, imaging features, and clinical implications significantly differ. CASE SUMMARY: A 16-year-old primigravida young woman was evaluated at 23 5/7 weeks' gestation in the fetal cardiology clinic for evaluation of a suspected thoracic cyst. Fetal echocardiography and magnetic resonance imaging demonstrated a large aneurysm arising from dilated coronary sinus with impressive posterior and inferior extension without persistent left superior vena cava. No hydrops, arrhythmia, or pericardial effusion were present. Postnatal echocardiography and computed tomography angiography confirmed a rare presentation of a coronary sinus aneurysm. DISCUSSION: Coronary sinus aneurysms arise from abnormal venous wall development or hemodynamic stress and must be distinguished from ventricular or atrial outpouchings, which carry variable risks of rupture, arrhythmia, or hydrops. Early fetal diagnosis permits accurate classification, anticipatory counseling, and tailored postnatal management. TAKE-HOME MESSAGES: This case illustrates the importance of distinguishing coronary sinus aneurysm from ventricular or atrial aneurysms. Prenatal recognition facilitates accurate diagnosis, risk assessment, counseling, and delivery planning.

JACC Case Reports
Phoenix Children's Hospital (US)
Good health and well-being
Openalex Percentile: Top 21%
Kawasaki Disease and Coronary Complications
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