# Cor Triatriatum Dexter With a Sinus Venosus Atrial Septal Defect in a 50-Year-Old Woman: A Case Report

**Authors:** Hasan Kazma, Malak Fakih, Ali Raad, Aalaa Saleh, Malek Mohammed

PMC · DOI: 10.7759/cureus.53477 · Cureus · 2024-02-02

## TL;DR

A 50-year-old woman was diagnosed with a rare heart defect involving an atrial septal defect and a cor triatriatum dexter membrane, leading to heart failure and requiring surgical intervention.

## Contribution

This case highlights the diagnostic challenges and management of a rare congenital heart defect in an adult patient.

## Key findings

- Transthoracic echocardiography showed right chamber dilation, pulmonary hypertension, and a left-to-right shunt.
- Transesophageal echocardiography confirmed a sinus venosus ASD with an incomplete cor triatriatum dexter membrane.
- Surgical intervention was recommended due to the complexity of the defect for percutaneous repair.

## Abstract

The diagnosis of atrial septal defect (ASD) may be delayed until adulthood or even later in life as it is a well-tolerated congenital heart disease. If patients are not examined and investigated well in childhood, the diagnosis may be delayed until later in adulthood when patients present with palpitations and sometimes dyspnea due to the right chambers dilatation from right ventricular volume overload. In this report, we present a case of a 50-year-old female patient with symptoms of heart failure and atrial fibrillation who was found to have dilated right cardiac chambers, dilated pulmonary artery, severe tricuspid regurgitation, pulmonary hypertension, and a pulmonary-to-systemic flow ratio (Qp/Qs) of more than 1.5 by transthoracic echocardiography and Doppler, indicating left to right shunt at the atrial level. However, transthoracic echocardiography could not visualize the defect, and two-dimensional (2D) transesophageal echocardiography was done in this patient and documented the presence of a sinus venosus ASD with an incomplete cor triatriatum dexter membrane; all four pulmonary veins were identified going to the left atrium. Since the presence of an incomplete cor triatriatum dexter membrane (despite causing no symptoms) makes the percutaneous closure of the sinus venosus ASD and the percutaneous repair of tricuspid regurgitation very difficult, we decided to advise surgical ASD closure and tricuspid valve repair for the patient.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252), atrial fibrillation (MONDO:0004981), pulmonary hypertension (MONDO:0005149)

## Full-text entities

- **Diseases:** Cor Triatriatum Dexter (MESH:D003310), palpitations (MESH:D006331), atrial fibrillation (MESH:D001281), ventricular volume overload (MESH:D019190), pulmonary hypertension (MESH:D006976), Sinus Venosus (MESH:C548009), pulmonary artery (MESH:D000071079), tricuspid regurgitation (MESH:D014262), congenital heart disease (MESH:D006330), ASD (MESH:D006344), chambers (MESH:C535679), dyspnea (MESH:D004417), heart failure (MESH:D006333)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

21 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10910018/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC10910018/full.md

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Source: https://tomesphere.com/paper/PMC10910018