Cardiac tumors--diagnosis and surgical treatment

Andreas Hoffmeier1, Jürgen R Sindermann, Hans H Scheld

  • 1Department of Cardiothoracic Surgery, Division of Cardiac Surgery, University Hospital of Münster.

Abstract

Insights

Timely surgical intervention in specialized centers improves outcomes for patients with cardiac tumors. Early surgery is crucial for both benign and malignant heart tumors, especially atrial myxoma, to prevent serious complications.

Area of Science:

  • Cardiovascular Surgery
  • Oncology
  • Diagnostic Imaging

Background:

  • Primary cardiac tumors are rare, complicating treatment evidence development.
  • Malignant cardiac tumors pose significant therapeutic challenges due to limited data.

Purpose of the Study:

  • To review literature and present long-term outcomes for cardiac tumor surgery.
  • To highlight optimal treatment strategies for primary and metastatic cardiac tumors.

Main Methods:

  • Selective PubMed literature search using terms: "cardiac tumor," "heart tumor," "cardiac myxoma," and "cardiac sarcoma."
  • Analysis of surgical techniques and outcomes in 181 patients with cardiac tumors treated between 1989 and 2012.

Main Results:

  • Cardiac tumors present with nonspecific symptoms; diagnosis relies on clinical history, echocardiography, CT, and MRI.
  • Autopsy prevalence of cardiac tumors is 0.02%; 75% benign (myxoma most common), 25% malignant (angiosarcoma most common).
  • Five-year survival rates: 83% for benign, 30% for malignant, and 26% for metastases. Surgery was performed on 181 patients.

Conclusions:

  • Timely surgical management in specialized centers is recommended for all cardiac tumors.
  • Early intervention is critical for atrial myxoma to prevent embolic complications.
  • Prompt surgical treatment improves survival rates for both benign and malignant cardiac tumors.

Related Concept Videos

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...
805
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...
460
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...
753
Imaging Studies for Cardiovascular System V: CT01:28

Imaging Studies for Cardiovascular System V: CT

Cardiac computed tomography (CT) scanning is an advanced cardiac imaging technique that utilizes CT technology, with or without intravenous (IV) contrast, to produce accurate cross-sectional virtual slices of specific areas of the heart, coronary circulation, and major blood vessels such as the aorta, pulmonary veins, and arteries. The computer processes these slices to generate three-dimensional images. Multidetector CT (MDCT) is a rapid form of CT scanning that captures multiple slices...
671
Mitral Stenosis II: Clinical features and Diagnostic Tests01:23

Mitral Stenosis II: Clinical features and Diagnostic Tests

Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
557
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
952