Cor Triatriatum Sinister with Secundum Atrial Septal Defect

Authors

  • Md Suhail Alam Assistant Professor, Department of Cardiology, Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Saleh Ahmad Tahlil Assistant Professor, Department of Cardiology, Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Ayesha Rafiq Chowdhury Professor, Department of Cardiology, Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Shahh Jamal Hussain Professor, Department of Cardiology, Jalalabad Ragib-Rabeya Medical College, Sylhet
  • Md Atiqur Rahman Registrar, Department of Cardiology, Jalalabad Ragib-Rabeya Medical College Hospital, Sylhet
  • Tafhema Tarin Junior Consultant, Department of Paediatrics, Sylhet Women’s Medical College Hospital, Sylhet

DOI:

https://doi.org/10.3329/jmj.v21i1.78127

Keywords:

Congenital heart disease, Cor triatriatum sinister, Atrial septal defect

Abstract

Cor triatriatum is a rare congenital heart defect, while secundum atrial septal defect (ASD) is a relatively common congenital heart defect. Primary symptoms in an older patient may mimic reactive airway disease if the diagnosis is not made in infancy. We report a case of cor triatriatum sinister in a 2 year old child, previously diagnosed with recurrent upper respiratory tract infection (RTI), presenting to a paediatrician. The initial response to treatment with bronchodilators and corticosteroids was not responding, prompting a thorough evaluation. Subsequent imaging was done and diagnosed as cor triatriatum sinister with secundum ASD. When patients with this type of scenario do not respond adequately to classical conservative management, it would be better for a clinician or paediatrician to look for an alternative diagnosis, as in this case.

Jalalabad Med J 2024; 21 (1): 23-25

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Published

2025-07-21

How to Cite

Alam, M. S., Tahlil, S. A., Chowdhury, A. R., Hussain, S. J., Rahman, M. A., & Tarin, T. (2025). Cor Triatriatum Sinister with Secundum Atrial Septal Defect. Jalalabad Medical Journal, 21(1), 23–25. https://doi.org/10.3329/jmj.v21i1.78127

Issue

Section

Case Report