An atrial myxoma is a benign tumor of the heart, commonly found within the left and right atria on the interatrial septum.
The tumor is derived from multipotential mesenchymal cells and may cause a ball valve-type obstruction.
About 75% of myxomas occur in the left atrium of the heart, usually beginning in the wall that divides the two upper chambers of the heart. The rest are in the right atrium. Right atrial myxomas are sometimes associated with tricuspid stenosis and atrial fibrillation.
Myxomas are more common in women. About 10% of myxomas are passed down through families (inherited). Such tumors are called familial myxomas. They tend to occur in more than one part of the heart at a time, and often cause symptoms at a younger age than other myxomas.
Right atrial myxomas rarely produce symptoms until they have grown to be at least 13 cm (about 5 inches) wide.
Tests may include:
Myxomas may come back if surgery did not remove all of the tumor cells.
Although a myxoma is not cancer, complications are common. Untreated, a myxoma can lead to an embolism (tumor cells breaking off and traveling with the bloodstream), which can block blood flow. Myxoma fragments can move to the brain, eye, or limbs.
If the tumor grows inside the heart, it can block blood flow through the mitral valve and cause symptoms of mitral stenosis. This may require emergency surgery to prevent sudden death.
Causes
Myxomas are the most common type of primary heart tumor.[1]The tumor is derived from multipotential mesenchymal cells and may cause a ball valve-type obstruction.
About 75% of myxomas occur in the left atrium of the heart, usually beginning in the wall that divides the two upper chambers of the heart. The rest are in the right atrium. Right atrial myxomas are sometimes associated with tricuspid stenosis and atrial fibrillation.
Myxomas are more common in women. About 10% of myxomas are passed down through families (inherited). Such tumors are called familial myxomas. They tend to occur in more than one part of the heart at a time, and often cause symptoms at a younger age than other myxomas.
Symptoms
Symptoms may occur at any time, but most often they accompany a change of body position. Symptoms may include:- Shortness of breath with activity
- Platypnea - Difficulty breathing in the upright position with relief in the supine position
- Paroxysmal nocturnal dyspnea - Breathing difficulty when asleep
- Dizziness
- Fainting
- Palpitations - Sensation of feeling your heart beat
- Chest pain or tightness
- Sudden Death (In which case the disease is an autopsy finding)
- Cough
- Fever
- Cachexia - Involuntary weight loss
- General discomfort (malaise)
- Joint pain
- Blue discoloration of the skin, especially the fingers (Raynaud's phenomenon)
- Fingers that change color upon pressure or with cold or stress
- Clubbing - Curvature of nails accompanied with soft tissue enlargement of the fingers
- Swelling - any part of the body
- Presystolic heart murmur[2]
Diagnosis
A doctor will listen to the heart with stethoscope. A "tumor plop" (a sound related to movement of the tumor), abnormal heart sounds, or a murmur similar to the mid-diastolic rumble of mitral stenosis may be heard. These sounds may change when the patient changes position.Tests may include:
- Echocardiogram and Doppler study
- Chest x-ray
- CT scan of chest
- Heart MRI
- Left heart angiography
- Right heart angiography
- ECG—may show atrial fibrillation
Treatment
The tumor must be surgically removed. Some patients will also need their mitral valve replaced. This can be done during the same surgery.Myxomas may come back if surgery did not remove all of the tumor cells.
Prognosis
If the tumor grows inside the heart, it can block blood flow through the mitral valve and cause symptoms of mitral stenosis. This may require emergency surgery to prevent sudden death.
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