THE TRIATRIAL HEART (COR TRIATRIATUM) – RARE ADULT CONGENITAL HEART DEFECT

نویسندگان

چکیده

Background: Cor triatriatum is a rare congenital cardiac malformation. Prevalence only around 0.1% of the diagnosed cardiovascular malformations. Historically prevalence has been described 0.4% in autopsies patients with heart disease. It characterized by presence membrane, usually, endocardium and fibro-muscular tissue within one atrial chambers, dividing it into two, thereby giving appearance three chambers. Case report: A 72-year-old patient presented to our surgery department complaints rhythm disorders, palpitations shortness breath. The history mitral valve pathology. During last six months, she had progression these failure clinical manifestation reffered institution for valvle after selective coronary angiography. echocardiography showed an abnormal membrane left atrium, diagnosis cor was fully made via transesophageal echocardiography. There were associated significant tricuspid regurgitations. Conclusion: CTS/cor triatrium sinister/ acyanotic disease which rarely presents during adulthood. symptoms adults are similar those stenosis. prognosis CTS depends on size fenestration fibromuscular membrane. Corrective treatment choice CTS.

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ژورنال

عنوان ژورنال: Journal of IMAB

سال: 2022

ISSN: ['1312-773X']

DOI: https://doi.org/10.5272/jimab.2022284.4630