An Unusual Cause of Right Heart Dysfunction and High Output Heart Failure in a Young Woman.
Nicolás Ariza OrdoñezAntonia Pino MarínJuan Sebastián Bonilla CrespoAlberto NavarroGabriel Antonio OliverHector M MedinaJulián F ForeroPublished in: Journal of cardiovascular development and disease (2022)
A 35-year-old female presented to our emergency department with clinical signs of acute heart failure. Clinical workup identified severe right heart (RH) dilation and dysfunction with a crossing membrane structure in the right atrium. Right heart catheterization confirmed high output heart failure (HOHF), pulmonary hypertension (PH), and left-to-right blood shunting followed by the documentation of multiple liver and pulmonary arteriovenous malformations (AVMs). Hereditary Hemorrhagic Telangiectasia (HHT) diagnosis was made according to clinical criteria and was established as the cause of HOHF because of chronic volume overload from systemic to pulmonary shunts. With this illustrative case, we aim to discuss the broad spectrum of clinical manifestations of HHT and the unusual phenotype of HOHF secondary to HHT. This case also highlights the broad diagnosis of atrial echocardiographic abnormalities and cardiac structural distortion secondary to high output that can be misleading at imaging evaluation.
Keyphrases
- heart failure
- pulmonary hypertension
- acute heart failure
- emergency department
- atrial fibrillation
- left ventricular
- pulmonary artery
- oxidative stress
- pulmonary arterial hypertension
- left atrial
- cardiac resynchronization therapy
- early onset
- mitral valve
- mass spectrometry
- drug induced
- ejection fraction
- photodynamic therapy