Published online Jan 16, 2024. doi: 10.12998/wjcc.v12.i2.460
Peer-review started: November 26, 2023
First decision: December 5, 2023
Revised: December 11, 2023
Accepted: December 21, 2023
Article in press: December 21, 2023
Published online: January 16, 2024
Processing time: 45 Days and 15.4 Hours
Double-chambered left ventricle (DCLV) is an extremely rare congenital disease in which the left ventricle (LV) is divided by abnormal muscle tissue. Due to its rarity, there is a lack of data on the disease, including its diagnosis, treatment, and prognosis. Accordingly, we report a case in which DCLV was diagnosed and followed up.
A 45-year-old man presented to our hospital due to abnormal findings on an electrocardiogram recorded during a health check. He had no specific cardiac symptoms, comorbidities or relevant past medical history. Echocardiography revealed that the LV was divided into two by muscle fibers. There were no findings of ischemia on coronary angiography and coronary computed tomo
Asymptomatic, uncomplicated DCLV was diagnosed through multimodal imaging; however, a thrombus in the AC occurred during the follow-up. The findings highlight that multimodal imaging is essential in diagnosing DCLV, and that anticoagulation is important in its management.
Core Tip: Double-chambered left ventricle (DCLV) is a rare congenital heart disease. Due to its rarity, the detailed data of the disease are not yet sufficient. We report the progress of a case of DCLV diagnosed incidentally. DCLV was diagnosed using multimodal imaging including echocardiography, coronary angiography, and coronary computed tomography angiography. After one year of follow-up, a thrombus occurred in the accessory chamber. The thrombus resolved after anticoagulation was initiated, and the patient is undergoing follow-up. Through this case, we demonstrate the necessity of multimodal imaging in the diagnosis of DCLV, and the importance of anticoagulation in the management.
