Heart tumor


A tumor is any type of abnormal growth, whether cancerous (malignant) or noncancerous (benign). Tumors that originate in the heart are called primary tumors. They may develop in any of the heart tissues and may be cancerous or noncancerous. Primary heart tumors are rare, occurring in fewer than 1 of 2,000 people. In adults, about half of noncancerous primary heart tumors are myxomas. Myxomas usually develop in the heart's left upper chamber (atrium). They may develop from embryonic cells located in the inner layer (lining) of the heart's wall.


Heart tumors may cause no symptoms, minor symptoms, or symptoms of life-threatening heart malfunction, which resemble those of other heart diseases but which develop suddenly. For example, tumors may cause heart failure, abnormal heart rhythms (arrhythmias), or a decrease in blood pressure caused by bleeding into the pericardium. Heart murmurs develop in about half of the people who have tumors that develop near or on a heart valve (such as myxomas and fibromas), because blood does not flow through the valve normally. Noncancerous tumors can be as deadly as cancerous ones if they interfere with the function of the heart. Heart tumors, especially myxomas, may degenerate so that pieces of them break off and travel through the bloodstream (becoming emboli). Emboli may lodge in small arteries and block blood flow. Also, blood clots that form on the surface of tumors, such as myxomas, may break off as emboli and block arteries. Symptoms due to emboli depend on where the clot goes and therefore which tissues or organs are affected by the blocked artery.


Primary heart tumors are difficult to diagnose because they are relatively uncommon and because their symptoms resemble those of many other disorders. Doctors may suspect a primary heart tumor in people who have heart murmurs, abnormal heart rhythms, unexplained symptoms of heart failure, or unexplained fever (which may be due to a myxoma). Secondary heart tumors are suspected when people who have cancer elsewhere in the body come to a doctor with symptoms of heart malfunction. If a tumor is suspected, echocardiography (see Symptoms and Diagnosis of Heart and Blood Vessel Disorders: Echocardiography and Other Ultrasound Procedures) is usually performed to confirm the diagnosis. For this procedure, a probe that emits ultrasound waves is passed over the chest, producing an image of heart structures. If another view of the heart is needed, the probe can be passed down the throat into the esophagus to record signals from just behind the heart. This procedure is called transesophageal echocardiography. Computed tomography (CT) (see Symptoms and Diagnosis of Heart and Blood Vessel Disorders: Computed Tomography) or magnetic resonance imaging (MRI) (see Symptoms and Diagnosis of Heart and Blood Vessel Disorders: Magnetic Resonance Imaging) can provide additional information. Coronary angiography (see Symptoms and Diagnosis of Heart and Blood Vessel Disorders: Coronary Angiography)can produce an outline of a heart tumor that can be seen on x-rays, but this procedure is rarely needed. If a tumor is detected in the right side of the heart, a small sample may be removed for examination under a microscope (biopsy). The sample is removed with a catheter that is inserted into a vein, usually in the leg, and threaded toward the heart in a procedure called cardiac catheterization (see Symptoms and Diagnosis of Heart and Blood Vessel Disorders: Cardiac Catheterization and Coronary Angiography). This procedure helps doctors identify the type of tumor and select the appropriate treatment. Biopsy of tumors on the left side is rarely performed, because the risks of the procedure outweigh the benefits.


A single small noncancerous primary heart tumor can be surgically removed, usually resulting in a cure. If a large noncancerous primary tumor is significantly reducing blood flow through the heart, removal of the part of the tumor that does not grow into the heart wall may improve heart function. However, if a large part of the heart wall is involved, surgery may be impossible. In about half of newborns who have noncancerous rhabdomyomas, tumors regress without treatment; in the other half, the tumors do not grow any larger and do not require treatment. In infants and children, a fibroma may be successfully removed if it does not affect the wall between the ventricles (septum). Tumors that affect this wall usually also affect the electrical conduction system of the heart and cannot be surgically removed. Children with this type of tumor usually die of an abnormal heart rhythm at an early age. If a fibroma is large, blocks blood flow, and has grown into the surrounding tissue, heart transplantation may be required. Primary cancerous tumors cannot be surgically removed and are usually fatal; chemotherapy or radiation therapy is sometimes used. Noncancerous tumors in the pericardium can be removed surgically, but cancerous tumors are not removed, as they have usually spread elsewhere in the body. If the tumor secretes fluid that interferes with heart motion, this fluid can be drained with a small plastic tube inserted by needle into the space between the pericardium and the heart (the pericardial space). Sometimes drugs are injected into the pericardial space to slow the tumor's growth.