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An Adult Patient of Double‐Chambered Right Ventricle with Ventricular Septal Defect Incidentally Diagnosed after Presentation with Acute Myocardial Infarction
Author(s) -
Shankarappa Ravindranath K.,
Patra Soumya,
Karur Satish,
Singh Ajitpal,
Nanjappa Manjunath C.,
Chandrasekaran Dhanlakshmi
Publication year - 2013
Publication title -
echocardiography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.404
H-Index - 62
eISSN - 1540-8175
pISSN - 0742-2822
DOI - 10.1111/echo.12334
Subject(s) - medicine , cardiology , ventricle , myocardial infarction , presentation (obstetrics) , right coronary artery , coronary artery disease , stenosis , radiology , coronary angiography
The double‐chambered right ventricle ( DCRV ) is a rare congenital heart disease caused by hypertrophic anomalous muscle bands that divide the ventricular cavity, resulting in the formation of a high‐pressure proximal chamber and other low‐pressure distal one. Because of its evolving nature, its diagnosis is usually made during childhood/adolescence and very rarely during adulthood. It accounts for approximately 0.5–1% of patients with congenital heart disease. We report a case of a 50‐year‐old man who presented to us with acute inferior wall myocardial infarction ( MI ). Echocardiography revealed the features of DCRV and ventricular septal defect. Coronary angiogram revealed significant stenosis in right coronary artery. This is the first case where an adult patient with DCRV incidentally diagnosed after presentation with acute MI and had undergone successful coronary angioplasty.

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