ISSN 1016-5169 | E-ISSN 1308-4488
Accessory Mitral Valve Tissue in Both Obstructive and Nonobstructive Hypertrophic Cardiomyopathy Cases [Turk Kardiyol Dern Ars]
Turk Kardiyol Dern Ars. 2025; 53(3): 206-210 | DOI: 10.5543/tkda.2024.15691

Accessory Mitral Valve Tissue in Both Obstructive and Nonobstructive Hypertrophic Cardiomyopathy Cases

İrem Türkmen1, Arda Güler1, Sezgin Atmaca1, İffet Doğan2, Gamze Babur Güler1
1Department of Cardiology, University of Health Sciences, Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkiye
2Department of Radiology, University of Health Sciences, Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkiye

Accessory mitral valve tissue (AMVT) is a rare congenital cardiac anomaly often associated with other congenital heart defects. Typically diagnosed in childhood, its presence in adulthood is exceptionally rare, especially in patients with hypertrophic cardiomyopathy (HCM). The coexistence of these two conditions can complicate the diagnosis, particularly in patients with left ventricular outflow tract (LVOT) gradient formation. This case series highlights the importance of multimodal imaging in accurately identifying AMVT, differentiating it from other conditions, and determining the various morphologies of AMVT.

Keywords: Accessory mitral valve tissue, echocardiography, hypertrophic cardiomyopathy

















Corresponding Author: İrem Türkmen
Manuscript Language: English
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