Key result
Cadaveric dissection reveals an absent tricuspid valve septal leaflet likely causing chronic TR and cardiomegaly.
Why the study?
Reports of absent tricuspid valve leaflets are exceedingly uncommon and have primarily involved the anterior or posterior leaflet, with isolated absence of the septal leaflet in adulthood not previously described.
Case Report (n=1)
No
This case report documents a previously undescribed isolated absence of the septal tricuspid leaflet in an adult, highlighting a rare structural variant that can lead to chronic tricuspid regurgitation and cardiomegaly.
The heart functions as a coordinated four-chambered pump, with four valves ensuring unidirectional blood flow. The tricuspid valve, located between the right atrium and right ventricle, consists of anterior, posterior, and septal leaflets that coapt during systole to prevent retrograde flow. Valvular disorders may result in stenosis or regurgitation, thereby increasing cardiac workload and predisposing to chamber dilation and heart failure. Congenital abnormalities, including partial or complete leaflet absence, are rare but can significantly disrupt normal hemodynamics. Reports of absent tricuspid valve leaflets are exceedingly uncommon and have primarily involved the anterior or posterior leaflet. During the thoracic dissection of a 41-year-old female body donor with a reported history of cardiovascular disease, cardiomegaly was identified. Gross examination revealed marked right atrial and ventricular enlargement. Internal inspection demonstrated a complete absence of the septal leaflet of the tricuspid valve, with intact anterior and posterior leaflets. Additional findings included dilation of the superior and inferior venae cavae, hypertrophied right atrial pectinate muscles, smooth and flattened right ventricular trabeculae carneae, and heterogeneous right ventricular myocardial thickness. The left heart structures were largely unremarkable aside from calcification of the mitral valve. Isolated absence of the septal tricuspid leaflet in adulthood has not been previously described. Loss of septal leaflet coaptation likely resulted in chronic tricuspid regurgitation, progressive right-sided volume overload, compensatory chamber dilation, and eventual cardiomegaly. Recognition of such rare structural variants is important for accurate imaging interpretation and surgical planning, particularly given potential distortion of critical landmarks such as the Triangle of Koch.
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Felsted et al. (2026) conducted a case report in Cardiomegaly with absent tricuspid septal leaflet (n=1). Cadaveric dissection of a 41-year-old female donor revealed cardiomegaly and a complete absence of the tricuspid valve septal leaflet, likely causing chronic tricuspid regurgitation.
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