Key result
Single-ventricle palliation successfully manages rare congenital tricuspid valve calcification causing inflow obstruction and RV hypoplasia.
Case Report (n=1)
Congenital valvular calcification is an extremely rare condition that can cause severe inflow obstruction and ventricular hypoplasia, which may be successfully managed with single-ventricle palliation.
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Alerts to inflow obstruction risks in rare congenital tricuspid calcification; leaves open optimal palliation strategies.
Fetal echocardiography demonstrated a hyperechogenic lesion (possibly calcification) obstructing the tricuspid inflow along with hypoplasia of the right ventricle (RV) and duct-dependent pulmonary circulation. Postnatal inflow along with hypoplasia of the right ventricle (RV) and duct-dependent pulmonary circulation. Postnatal surgical exploration, only minimal antegrade flow was established. Histopathology confirmed degenerative valvar tissue with dense calcification. Eventually, due to persistent inflow restriction and inadequate RV growth, the infant underwent single-ventricle palliation (bidirectional Glenn shunt) with uneventful follow-up after the procedure. This case highlights the extreme rarity of congenital valvular calcification, its possible developmental and genetic associations, and the hemodynamic significance of inflow obstruction in causing ventricular hypoplasia.
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Pandey et al. (2026) conducted a case report in Congenitally calcified tricuspid valve with right ventricular hypoplasia (n=1). Single-ventricle palliation (bidirectional Glenn shunt) was evaluated. A rare case of congenital tricuspid valve calcification causing inflow obstruction and right ventricular hypoplasia was successfully managed with single-ventricle palliation.
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