Primary tumors of the heart are extremely rare tumors that arise from the normal tissues that make up the heart. This is in contrast to secondary tumors of the heart, which are typically either metastatic from another part of the body, or infiltrate the heart via direct extension from the surrounding tissues.
Contents
1Types
1.1Benign
1.2Malignant
1.3Valvular
2Prognosis
3See also
4References
5External links
Types
Micrograph of a papillary fibroelastoma, a benign tumor of heart valves. H&E stain.
Micrograph of an atrial myxoma, the most common primary tumor of the heart.
Benign
The most common primary tumor of the heart is the myxoma. In surgical series, the myxoma makes up as much as 77% of all primary tumors of the heart.[1] Less common tumors of the heart include lipoma and cystic tumor of the atrioventricular nodal region.
Malignant
About 20 percent of primary tumors of the heart are malignant in nature.[1] Malignant tumors of the heart include rhabdomyosarcomas, angiosarcomas, myxosarcomas, fibrosarcomas, leiomyosarcomas, reticulum cell sarcomas, desmoplastic small round cell tumor, and liposarcomas. The cardiac sarcomas may occur at any age, but are more commonly seen in individuals in their 20s to 40s. They occur equally in males and females.
Valvular
A subset of the primary tumors of the heart are tumors that are found on the valves of the heart. Tumors that affect the valves of the heart are found in an equal distribution among the four heart valves.[1] The vast majority of these are papillary fibroelastomas. Primary tumors of the valves of the heart are more likely to occur in males. While most primary tumors of the valves of the heart are not malignant, they are more likely to have symptoms related to the valve, including neurologic symptoms and (in a few cases) sudden cardiac death.
Prognosis
The vast majority of the tumors of the heart have a benign course and are not directly fatal. However, even the benign tumors of the heart can be lethal due to either direct extension into the electrical conduction system of the heart (causing complete heart block or a fatal dysrhythmia), or due to emboli from the tumor mass that may have lethal sequelae.
The malignant tumors of the heart have a worse prognosis. Cardiac sarcomas generally lead to death within 2 years of diagnosis, due to rapid infiltration of the myocardium of the heart and obstruction of the normal flow of blood within the heart.[2][3]
See also
Cardiac fibroma
References
^ abcMolina JE, Edwards JE, Ward HB (1990). "Primary cardiac tumors: experience at the University of Minnesota". Thorac Cardiovasc Surg. 38 Suppl 2: 183–91. doi:10.1055/s-2007-1014064. PMID 2237900.
^Burke AP, Cowan D, Virmani R (1992). "Primary sarcomas of the heart". Cancer. 69 (2): 387–95. doi:10.1002/1097-0142(19920115)69:2<387::AID-CNCR2820690219>3.0.CO;2-N. PMID 1728367.
^Burke AP, Virmani R (1991). "Osteosarcomas of the heart". Am J Surg Pathol. 15 (3): 289–95. doi:10.1097/00000478-199103000-00009. PMID 1705103.
External links
Classification
D
v
t
e
Heart neoplasia (C38.0/D15.1, 164.1/212.7)
Primary
Papillary fibroelastoma
Rhabdomyoma
Angiosarcoma
Teratoma
Cystic tumour of the atrioventricular nodal region
Other
Myxoma
Atrial
Lipoma
Secondary
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