- What is Atrial Myxoma
- Statistics on Atrial Myxoma
- Risk Factors for Atrial Myxoma
- Progression of Atrial Myxoma
- Symptoms of Atrial Myxoma
- Clinical Examination of Atrial Myxoma
- How is Atrial Myxoma Diagnosed?
- Prognosis of Atrial Myxoma
- How is Atrial Myxoma Treated?
- Atrial Myxoma References
What is Atrial Myxoma
Atrial myxomas are heart tumours that are usually found in the left atrium.
Statistics on Atrial Myxoma
It is very rare; the incidence is less than 0.14% (< 5 in 10,000). However, atrial myxoma is the most common of all primary cardiac tumours.
Risk Factors for Atrial Myxoma
Peak incidence is in the 30-60 year age group with higher rates seen in females than in males. Some familial patterns of atrial myxoma have been seen.
Progression of Atrial Myxoma
The tumour grows slowly and eventually may close the mitral valve and thus may cause pulmonary hypertension and right heart failure from back pressure. The tumour may also become infected or become a source of thrombi (clots) which then embolise, potentially causing a stroke or heart attack.
Symptoms of Atrial Myxoma
How is Atrial Myxoma Diagnosed?
Prognosis of Atrial Myxoma
Although atrial myxomas have the potential to embolise and to grow elsewhere, they are not believed to be able to spread to other sites. Surgical resection is usually curative and the main mortality and morbidity carried by these tumours is associated with complications such as embolisation – strokes or heart attacks.
How is Atrial Myxoma Treated?
Surgical excision is the treatement of choice and is usually curative.
Atrial Myxoma References
- Schlant RC, Alexander RW, Fuster V (eds). Hurst’s The Heart (8th edition). New York, NY: McGraw-Hill; 1994. Book
- Kumar P, Clark M (eds). Clinical Medicine (4th edition). Edinburgh: WB Saunders Company; 1998. Book