Atrial Myxoma Essay

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Atrial myxoma was first documented as a simple vascular growth in the heart by TW King in 1845. Now, over a hundred seventy years later, it can be describe as a benign tumor of connective tissue typically in the atrium. Although it possesses characteristic of cancerous cells and is generally included in cardiac cancer because of their similarities, it is often not considered cancer because it is benign. Heart tumors and cancers are very rare, accounting for only 0.2% of tumors found in the body, due to the fact that heart cells divide mostly while we are still fetuses. Once the heart is developed they divide less frequently leaving fewer opportunity for failure in the cell cycle. Because they are rare, there are still numerous unknown …show more content…

Overall though, atrial myxoma has a one in two thousand ratio of incidence and females of sex are more liking to be diagnosed by 75%. It is estimated that one in every ten occurrences are familial myxoma (hereditary) but this tends to be evenly distributed between sexes. These nicknamed “family myxomas” can even occur in multiple places of the heart at once but the patient tends to show symptoms at a younger age.
In normal circumstances, generic symptoms are reported. Things like orthopnea, chest pains and tightness, dizziness, palpitations, and rapid weight loss are reported. For severer cases clubbing of fingers, bluish tents, fainting, and dyspnea are expected. Different symptoms can be associated with different locations of the myxoma. For example, in the left atria, more patients experience head pain and pulmonary edema with the myxoma, while in the right atria, they have greater symptoms of right heart failure. It has also been expressed that changes in body position and fast movements can bring on symptoms. Symptoms can be experienced in a few different ways. Some people report having them continually everyday whiles others come and

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