ESSENTIALS OF DIAGNOSIS
A rare but critical diagnosis in the evaluation of cardiac masses.
The history, physical examination, and imaging characteristics can yield valuable diagnostic clues.
Diagnostic confirmation requires tissue biopsy.
Cardiac tumors, although considered a rare diagnostic entity, provide unique insight into the anatomic and pathophysiologic functioning of the heart. Reminiscent of benign, malignant, and metastatic neoplasms elsewhere in the body, theses tumors herald their presence by the secondary effects produced from enlarging within the confines of cardiac chambers and tissues. Because they rarely cause symptoms, cardiac tumors are generally unsuspected and may be discovered incidentally during evaluation of an unrelated condition. This chapter will help guide the astute clinician, focusing on when to consider this diagnosis and how to obtain the appropriate cardiovascular imaging studies. There are a wide variety of common cardiac tumors (Table 32–1).
Table Graphic Jump Location Table 32–1.Classification of Common Cardiac Tumors ||Download (.pdf) Table 32–1. Classification of Common Cardiac Tumors
|Primary Cardiac Tumors |
Hamartoma (oncocytic cardiomyopathy)
Sarcoma: includes angiosarcoma, rhabdomyosarcoma, fibrosarcoma, osteosarcoma, leiomyosarcoma, liposarcoma, synovial sarcoma
Malignant fibrous histiocytoma
Benign or Malignant Tumors
Mesothelioma (includes cystic tumor of the atrioventricular node)
|Secondary Cardiac Tumors |
| Metastasis to the heart and pericardium: commonly from malignant melanoma or neoplasms of the lung, hematopoietic system, gastrointestinal tract, kidney, breast, thyroid, and soft tissue |
PRIMARY CARDIAC TUMORS
Primary tumors of the heart are rare, with a prevalence of 0.02% reported in combined data from multiple large autopsy series. Although cardiac myxoma has been traditionally reported as the most frequent tumor type in adults, increasing utilization of imaging studies has revealed a higher frequency of papillary fibroelastomas than previously known. In the pediatric population, rhabdomyomas represent the most common type of primary cardiac tumor (Table 32–2).
Table Graphic Jump Location Table 32–2.Primary Cardiac Tumors: Location and Features ||Download (.pdf) Table 32–2. Primary Cardiac Tumors: Location and Features
|Cardiac Tumor ||Typical Location ||Interesting Features/Associations |
|Myxoma ||Left atrium ||Carney complex; constitutional symptoms |
|Papillary fibroelastoma ||Cardiac valves ||Can present with sudden death from coronary ostial obstruction |
|Fibroma ||Left ventricular myocardium ||Very large tumors that exert a mass effect |
|Rhabdomyoma ||Cardiac chambers ||Tuberous sclerosis |
|Angiosarcoma ||Right atrium ||Highly aggressive tumor |
|Rhabdomyosarcoma ||Cardiac chambers ||Commonest pediatric malignancy |
|Fibrosarcoma ||Left atrium ||White fish flesh tumor |
|Leiomyosarcoma ||Smooth muscle cells of pulmonary veins and arteries ||Epstein-Barr virus in immunosuppressed patients |
|Lymphoma ||Right heart chambers ||Immunocompromised patients |
|Paraganglioma ||Pericardium; left atrial wall ||Majority are hormonally inactive |
|Teratoma ||Pericardium ||Contain elements from all three germ cell layers |
A. Benign Cardiac Tumors
The overwhelming majority of primary cardiac tumors, approximately 75% to more than 90%, are benign, and may arise ...