Right Atrial Cardiac Hemangioma: A Multidisciplinary Pathway From Symptoms to Surgery

Jade Gourmelon1, Valentin Loobuyck1, Valentina Silvestri2

  • 1Department of Cardiac Surgery, University of Lille, Centre Hospitalier Universitaire Lille, Lille, France.

JACC. Case Reports
|January 17, 2025
PubMed

Insights

A rare cardiac capillary hemangioma caused right heart failure in a 76-year-old man. Advanced imaging challenges in localizing intracardiac masses, like this vascular tumor, are highlighted.

Area of Science:

  • Cardiology
  • Cardiovascular Surgery
  • Diagnostic Imaging

Background:

  • Right heart failure can stem from various causes, including intracardiac masses.
  • Cardiac tumors are rare, with hemangiomas being an uncommon subtype.
  • Accurate localization and characterization of cardiac masses are crucial for diagnosis and treatment planning.

Purpose of the Study:

  • To report a case of de novo right heart failure secondary to an intracardiac capillary hemangioma.
  • To illustrate the diagnostic challenges associated with rare cardiac masses despite advanced imaging.
  • To emphasize the importance of surgical confirmation for definitive diagnosis.

Main Methods:

  • A 76-year-old male patient presenting with new-onset right heart failure.
  • Multimodality cardiac imaging, including echocardiography and positron emission tomography (PET) scan.
  • Surgical resection of the intracardiac mass via right anterior mini-thoracotomy.

Main Results:

  • Echocardiography identified a mass near the right atrium, but its precise location was unclear.
  • PET scan indicated hypermetabolic activity, suggesting a vascular tumor.
  • Histopathological examination of the resected mass confirmed a capillary hemangioma.

Conclusions:

  • Cardiac capillary hemangiomas can present as right heart failure.
  • Advanced imaging modalities may still face challenges in precisely localizing and characterizing rare intracardiac masses.
  • Surgical resection remains essential for definitive diagnosis and management of such rare cardiac tumors.

Related Concept Videos

Cardiac Catheterization II: Right Heart Catheterization01:21

Cardiac Catheterization II: Right Heart Catheterization

Right Heart Catheterization: An OverviewRight heart catheterization is an invasive diagnostic procedure that measures right-sided cardiac and pulmonary artery pressures, calculates cardiac output, and identifies intracardiac shunts. It provides detailed hemodynamic data essential for diagnosing and managing various cardiovascular conditions, such as pulmonary hypertension.Access SitesCommon access sites for right heart catheterization include the internal jugular vein in the neck region, the...
Mitral Stenosis III: Medical Management01:26

Mitral Stenosis III: Medical Management

Mitral stenosis, a condition marked by the narrowing of the mitral valve, necessitates an integrated approach for effective management. This approach includes preventative measures, medical therapy, and surgical interventions to reduce symptoms and prevent complications.PreventionPrevention of mitral stenosis primarily focuses on reducing the incidence of bacterial infections, particularly streptococcal infections, which can lead to rheumatic fever and subsequent valvular damage. Timely...
Aortic Regurgitation III: Medical Management01:25

Aortic Regurgitation III: Medical Management

Aortic regurgitation (AR) is when the aortic valve does not close or seal properly, leading to backward blood circulation from the aorta into the left ventricle during diastole. Common causes of AR include rheumatic heart disease, congenital valve defects, and aortic root dilation. Managing AR requires a multifaceted approach to alleviate symptoms, preserve left ventricular function, and address the underlying cause of the regurgitation. Patients with symptomatic AR or significant left...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
Cardiomyopathy VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...