eMedicine Specialties > Pediatrics: Cardiac Disease and Critical Care Medicine > Cardiology
Cardiac Tumors: Differential Diagnoses & Workup
Updated: Nov 10, 2008
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Differential Diagnoses
Other Problems to Be Considered
Collagen vascular diseases
Mural thrombus
Cerebrovascular accident
Vasculitis (ie, lupus, polyarteritis)
Mitral valve stenosis
Workup
Laboratory Studies
- CBC count with differential should be normal in benign cardiac tumors. In malignant tumors, any kind of blood count abnormality can be present in these patients. For example, anemia is not an uncommon finding. Platelet count may be elevated or low, and WBC count may be high.
- Erythrocyte sedimentation rate (ESR) is a nonspecific marker for inflammation that may be normal or elevated; however, the ESR could be low in the presence of congestive heart failure (CHF).
- Liver function test findings are occasionally elevated because of severe right-sided heart failure or metastases.
- Creatine kinase-myocardial band (CK-MB) fraction levels have been found to be higher in patients who have both ventricular dysfunction and a cardiac tumor but not necessarily primary malignancies from the heart.
Imaging Studies
- Echocardiography
- This is the most cost-effective of all tests used to evaluate the anatomy of the heart. Echocardiography can provide important information about size, extension and/or invasion within and outside the heart, valvar involvement and/or competency, ventricular function, and pericardial effusion.
- It is very sensitive but not specific.
- Some of these tumors may be too small for echocardiographic detection, especially those leading to dysrhythmias.
- Transesophageal echocardiogram also is useful in detecting tumors in the left heart, especially in adults.
- Chest roentgenography: Cardiomegaly and pulmonary edema may present in cases of obstructive lesions. Certain neoplasms can have calcium deposition detected on the roentgenogram.
- MRI: MRI is a powerful tool in diagnosing tumors, evaluating their extent, and seeking metastases. It may delineate the area of the mass better than echocardiography because it has a larger field of observation. Contrast enhancement and multislice imaging can provide a 3-dimensional view of tissue. It also can help differentiate tumors from thrombi.
- CT scanning: Ultrafast CT scanning is gaining use in this area because it eliminates artifacts of heart motion seen with conventional CT scanning. CT is a powerful tool in evaluating the extent of the tumor and exhibits a high degree of tissue discrimination.
Other Tests
- ECG: Nonspecific changes are the most common findings; however, ST-T segment changes with strain patterns have been noticed in obstructive rhabdomyomas and fibromas. After surgery, these changes return to normal. Other patterns associated with ischemia also may be present. Diffuse low-voltage QRS, especially in the presence of pericardial effusion, can be seen. Arrhythmias may be the first presentation of an intracardiac tumor and occasionally are resistant to medical therapy. Other findings include intraventricular conduction delay and complete bundle branch block.
Procedures
- Endomyocardial biopsy is controversial and seldom useful in children because of the high possibility of false-negative results and the high possibility of metastasis during the procedure if a malignant tumor is present.
Histologic Findings
Benign tumors
Rhabdomyomas are a glycogenic degeneration of myocardial fibers and are thus considered hamartomas. They contain large vacuolated cells filled with glycogen. Their microscopic hallmark, the spider cell, displays eccentric nuclei, granular cytoplasm with a central cytoplasmic mass, and fine fibrillar processes that radiate to the periphery, giving the appearance of a spider in a web. Because the cytoplasm is rich in glycogen, it stains positive with periodic acid-Schiff reagent. Rhabdomyositis is a rare form of cardiomyopathy. In this pathology, microscopic changes in the muscle and conduction system are evident, yet gross anatomic findings are rare.
Cardiac fibromas consist of elongated fibroblasts, with fibrous tissue and collagen. Occasionally, calcium can be seen using radiography or microscopically within the tumor. Mitosis is rarely seen in this type of tumor.
Myxoma has a characteristic pattern of cells termed lipidic cells embedded in a myxoid stroma rich in glycosaminoglycans. These cells are multinucleated with pink cytoplasm. Typically, they present in clusters surrounding vascular structures. Calcium is present in approximately 10% of patients. Usually, the embolized material has a different pattern from the material at the center of the lesion, and cells resemble embryonic mesenchymal cells, similar to embryonic endocardial cushion tissue.
Teratomas, rarely malignant in children, form from 3 embryonic tissues that usually grow in the anterior mediastinum. These tumors should be differentiated from intrapericardial bronchogenic cysts because they may have the same gross appearance; the histologic difference is that bronchogenic cysts do not contain neuronal tissue, which is usually present in teratomas.
Hemangiomas are classified, based on the predominant type of proliferating vascularity, into hemangiomas (common) or lymphangiomas (extremely uncommon). The tumor contains endothelium-lined spaces that may have blood, lymph, or thrombi.
Malignant tumors
Angiosarcomas have variable vascular channels lined with atypical endothelial cells.
The histologic hallmark of rhabdomyosarcoma is the presence of cross-striations.
Fibrosarcomas are composed of a herringbone pattern of spindle-shaped cells with elongated blunt-ended nuclei and frequent mitoses.
More on Cardiac Tumors |
| Overview: Cardiac Tumors |
Differential Diagnoses & Workup: Cardiac Tumors |
| Treatment & Medication: Cardiac Tumors |
| Follow-up: Cardiac Tumors |
| Multimedia: Cardiac Tumors |
| References |
| « Previous Page | Next Page » |
References
Lam KY, Dickens P, Chan AC. Tumors of the heart. A 20-year experience with a review of 12,485 consecutive autopsies. Arch Pathol Lab Med. Oct 1993;117(10):1027-31. [Medline].
Kono T, Koide N, Hama Y, et al. Expression of vascular endothelial growth factor and angiogenesis in cardiac myxoma: a study of fifteen patients. J Thorac Cardiovasc Surg. Jan 2000;119(1):101-7. [Medline].
Butany J, Nair V, Naseemuddin A, et al. Cardiac tumours: diagnosis and management. Lancet Oncol. Apr 2005;6(4):219-28. [Medline].
Dhillon G, Rodriguez-Cruz E, Kathawala M, Alqassem N. Primary cardiac myofibroblastic sarcoma, case report and review of diagnosis and treatment of cardiac tumors. Bol Asoc Med P R. Jul-Dec 1998;90(7-12):130-3. [Medline].
Farooki ZQ, Ross RD, Paridon SM, et al. Spontaneous regression of cardiac rhabdomyoma. Am J Cardiol. Apr 15 1991;67(9):897-9. [Medline].
Gaumann A, Strubel G, Bode-Lesniewska B, Schmidtmann I, Kriegsmann J, Kirkpatrick CJ. The role of tumor vascularisation in benign and malignant cardiovascular neoplasms: a comparison of cardiac myxoma and sarcomas of the pulmonary artery. Oncol Rep. Aug 2008;20(2):309-18. [Medline].
Le Guyader A, Laskar M. Removal of left ventricular tumors by a transaortic transvalvular approach with the help of thoracoscopic instruments. J Thorac Cardiovasc Surg. Aug 2008;136(2):537-8. [Medline].
Lopez M, Pinto A, Moreno V, Diaz M, Gonzalez Baron A. Primary cardiac osteosarcoma. Clin Transl Oncol. Aug 2008;10(8):515-6. [Medline].
Ludomirsky A. Cardiac tumors. In: Bricker JT, Fisher DJ, eds. The Science and Practice of Pediatric Cardiology. Vol 2. 9th ed. Williams & Wilkins; 1998:1885-93.
Martinez Quesada M, Trujillo Berraquero F, Almendro Delia M, et al. [Cardiac hamartoma. Case report and literature review]. Rev Esp Cardiol. Apr 2005;58(4):450-2. [Medline].
Marx GR. Cardiac Tumors. In: Emmanouilides GC, Gutgesell HP, Riemenschneider TA, Allen HD, eds. Moss and Adams Heart Disease in Infants, Children, and Adolescents: Including the Fetus and Young Adult. Vol 2. 5th ed. Baltimore, MD: Williams & Wilkins; 1995:1773-86.
McAllister HA, Fenoglio JJ Jr. Tumors of the cardiovascular system: atlas of tumor pathology, second series. In: Washington, DC: Armed Forces Institute of Pathology. 1978.
Padalino MA, Basso C, Milanesi O, et al. Surgically treated primary cardiac tumors in early infancy and childhood. J Thorac Cardiovasc Surg. Jun 2005;129(6):1358-63. [Medline].
Piazza N, Chughtai T, Toledano K, et al. Primary cardiac tumours: eighteen years of surgical experience on 21 patients. Can J Cardiol. Dec 2004;20(14):1443-8. [Medline].
Rodriguez-Cruz E, Cintron-Maldonado RM, Bercu BA. Primary cardiac osteogenic sarcoma treated with heart transplantation. Bol Asoc Med PR. 1999;91 (7-12):98-99. [Medline].
Rodriguez-Cruz E, Cintron-Maldonado RM, Forbes TJ. Treatment of primary cardiac malignancies with orthotopic heart transplantation. Bol Asoc Med P R. Apr-Aug 2000;92(4-8):65-71. [Medline].
Takach TJ, Reul GJ, Ott DA, Cooley DA. Primary cardiac tumors in infants and children: immediate and long-term operative results. Ann Thorac Surg. Aug 1996;62(2):559-64. [Medline].
Tatli S, Lipton MJ. CT for intracardiac thrombi and tumors. Int J Cardiovasc Imaging. Feb 2005;21(1):115-31. [Medline].
Tazelaar HD, Locke TJ, McGregor CG. Pathology of surgically excised primary cardiac tumors. Mayo Clin Proc. Oct 1992;67(10):957-65. [Medline].
Wu XM, Hu CZ, Li N, et al. [Relationship of serum level of creatine kinase of MB type to cardiac function of patients with advanced tumors and its prognostic value]. Ai Zheng. Apr 2005;24(4):506-8.abs. [Medline].
Further Reading
Keywords
cardiac tumors, cardiac neoplasm, heart tumors, heart neoplasm, neoplasm of the heart, rhabdomyoma, fibroma, myxoma, teratoma, sarcoma, angiosarcoma, cancer, cardiac mass, congenital heart failure, CHF, jugular venous distention, ascites, pericardial effusion, syncope, shortness of breath, vena cava syndrome, pulmonary embolism, restrictive cardiomyopathy, tuberous sclerosis, Carney syndrome, vascular tumors, hemangiomas, lymphangiomas, heart block, lipomas, papillary tumors, leiomyomas, mesotheliomas, fibroelastomas, fibroelastic papillomas, benign cystic tumors, rhabdomyosarcoma
Differential Diagnoses & Workup: Cardiac Tumors