# Quadricuspid Right Atrioventricular Valve: A Cadaveric Case Report

**Authors:** Tanner Buckway, Mallory Weed, Alejandra Tobon, Amberly Reynolds

PMC · DOI: 10.7759/cureus.92930 · Cureus · 2025-09-22

## TL;DR

A rare case of a four-cusped tricuspid valve was found in a cadaver, showing how it can lead to heart dysfunction and complications.

## Contribution

This case report documents a rare quadricuspid right atrioventricular valve with associated anatomical and functional abnormalities.

## Key findings

- The cadaver had a quadricuspid tricuspid valve with an accessory papillary muscle and right atrial dilation.
- Right ventricular hypertrophy and poor valve coaptation suggest chronic valvular dysfunction and regurgitation.
- The case highlights the potential for degenerative changes in congenital valve anomalies in the elderly.

## Abstract

Quadricuspid heart valve anomalies are rare congenital malformations, typically affecting the aortic valve; involvement of the right atrioventricular (tricuspid) valve is exceedingly uncommon. Embryologically, the tricuspid valve forms through complex fusion and delamination processes involving the endocardial cushions.

This case describes a quadricuspid right atrioventricular valve identified during routine cadaveric dissection in an elderly male. Gross examination revealed four distinct cusps and an accessory papillary muscle, along with right atrial dilation, near-complete atrophy of the right auricle, right ventricular hypertrophy, and evidence of poor valve coaptation. These findings, combined with signs of cardiomegaly, suggest significant valvular dysfunction during life, likely contributing to chronic tricuspid regurgitation. During the gross examination, valvular distortion was noted, highlighting the potential for secondary degenerative changes superimposed upon congenital structural anomalies, particularly in the elderly.

Recognition of such anomalies is essential, as they may predispose individuals to valvular incompetence, right-sided heart dysfunction, and other clinical complications. Early identification and characterization of these rare malformations may influence clinical management and surgical decision-making.

## Full-text entities

- **Diseases:** heart dysfunction (MESH:D006331), right ventricular hypertrophy (MESH:D017380), malformations (MESH:C564254), cardiomegaly (MESH:D006332), atrial dilation (MESH:C563984), Quadricuspid heart valve anomalies (MESH:D000082902), congenital malformations (OMIM:163000), atrophy of the right auricle (MESH:D001284), congenital structural anomalies (MESH:D020914), tricuspid regurgitation (MESH:D014262), valvular distortion (MESH:D006311), Atrioventricular Valve (MESH:D006349)

## Full text

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## Figures

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## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12542920/full.md

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Source: https://tomesphere.com/paper/PMC12542920