A double-chambered left ventricle with a giant thrombus: a case report.
Weixia NieJian HeMin-Jie LuPublished in: European heart journal. Case reports (2023)
A DCLV is an extremely rare congenital heart disease that is often asymptomatic and undiagnosed until adulthood. The aetiology of DCLV is still unclear; however, some reports have suggested that it may be related to a hypoplasia of the regional myocardial intra-trabecular sinusoids or an intra-myocardial aneurysm during the embryonic period. Additionally, some cases have indicated that DCLV may be a subtype of genetic cardiomyopathies. A DCLV is characterized by a subdivision of the left ventricle into two chambers by an abnormal septum or by muscle bands. This case report introduces a patient with DCLV and a giant thrombus, in which CMR imaging plays an important role in both diagnosis and differential diagnosis.
Keyphrases
- congenital heart disease
- case report
- left ventricular
- high resolution
- coronary artery
- pulmonary artery
- rare case
- skeletal muscle
- mitral valve
- genome wide
- depressive symptoms
- bone mineral density
- heart failure
- adverse drug
- emergency department
- pulmonary hypertension
- body composition
- copy number
- early life
- mass spectrometry
- abdominal aortic aneurysm
- pulmonary arterial hypertension
- dna methylation
- electronic health record
- drug induced