Evidence map›Paper›PMID 41961033›Full record

ArticleJACC. Case reports2026

Unique Prenatal Diagnosis of a Coronary Sinus Aneurysm.

Zareh Torabyan, Christopher Lindblade, Michael Nguyen, Ryan Johnson

Abstract readCase Reports
In one paragraph

Article in JACC. Case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Zareh TorabyanDepartment of Pediatric Cardiology, Phoenix Children's Hospital, Phoenix, Arizona, USA. Electronic address: ztorabyan@phoenixchildrens.com.
Christopher LindbladeDepartment of Pediatric Cardiology, Phoenix Children's Hospital, Phoenix, Arizona, USA.
Michael NguyenDepartment of Pediatric Cardiology, Phoenix Children's Hospital, Phoenix, Arizona, USA.
Ryan JohnsonDepartment of Pediatric Cardiology, Phoenix Children's Hospital, Phoenix, Arizona, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital 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.

Indexed as

computed tomographycongenital heart defectechocardiography

Identifiers

PMID41961033
PMCPMC13309719

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.