ArticleCureus2025
Delayed Diagnosis of Cor Triatriatum Dexter: A Case Report and Comprehensive Review of Embryology, Imaging, and Management.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Cor Triatriatum Dexter: The Largest Comprehensive Review in the Field on 124 Worldwide Cases (1968-Now).Journal of cardiovascular development and disease · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cor triatriatum dexter (CTD) is a rare congenital cardiac anomaly resulting from the persistence of the right valve of the sinus venosus, leading to partial or complete partitioning of the right atrium. It accounts for a minority of congenital heart defects and may present with various clinical features ranging from asymptomatic incidental findings to severe right-sided heart failure. We report the case of a 45-year-old female with longstanding exertional dyspnea, peripheral edema, hepatomegaly, and severe bilateral varicose veins. Abdominal imaging revealed features of hepatic congestion, whereas echocardiography revealed a markedly dilated inferior vena cava (IVC) and a membrane at the junction of the IVC and right atrium. Transesophageal echocardiography confirmed a fibromuscular membrane consistent with CTD, partially obstructing systemic venous return. The patient also had a preserved left ventricular systolic function. CTD arises from incomplete regression of the embryonic right venous valve. The degree of membrane perforation influences the severity of obstruction and clinical symptoms. While an incomplete CTD can be clinically silent, significant septation may lead to elevated right atrial pressures and systemic venous congestion. This case emphasizes the diagnostic utility of multimodality imaging in adults with unexplained right-sided heart failure symptoms and highlights CTD's potential role in chronic venous disorders. This case adds to the limited literature on conservatively managed adult CTD, highlighting the impact of financial barriers on therapeutic decision-making. CTD, although rare, should be considered in the differential diagnosis of right-sided congestion in adults, particularly when it is accompanied by unexplained IVC dilation, hepatic congestion, and chronic venous insufficiency. Early recognition through echocardiography and other imaging modalities is essential for guiding appropriate management and avoiding misdiagnosis.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.