There are several pheochromocytoma symptoms. These symptoms may vary from person to person. In many cases, symptoms are not noticeable and may occur without the patient being aware of the problem. These symptoms include a high blood pressure, sweating, anxiety, and rapid heartbeat. However, in some cases, pheochromocytomas are associated with these classic symptoms. Listed below are some of these signs and symptoms.
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Surgical treatment for pheochromocytoma involves surgical removal of the tumor. It is a highly effective treatment when detected in its early stages. Surgery can also be combined with radiopharmaceutical therapy or chemotherapy. In some cases, an experienced physician may advise regular monitoring. If left untreated, pheochromocytoma can lead to serious complications including high blood pressure, arrhythmia, and heart failure. In some cases, the tumor may spread to the bones.
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Besides being an aggressive cancer, pheochromocytoma can be hereditary. Hereditary syndromes such as multiple endocrine neoplasia (MEN-2) can result in pheochromocytoma. However, patients with this type of tumor should seek genetic testing to rule out other causes of their disease. However, genetic factors are not a factor in all cases of pheochromocytoma.
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Patients with suspected pheochromocytoma may undergo blood tests to detect abnormal levels of adrenaline and noradrenaline. Imaging tests may also be used to diagnose pheochromocytoma. Imaging of the abdomen will confirm the presence of pheochromocytoma, which typically has characteristic features. If pheochromocytoma is a hereditary disease, genetic tests may be conducted to screen family members.
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A diagnosis of pheochromocytoma is often delayed by symptoms of other diseases. A typical patient will experience paroxysmal hypertension, sweating, and palpitations. Although pheochromocytoma symptoms may be sporadic, some people experience them repeatedly. If the condition continues untreated, it could lead to a heart attack or a stroke.
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Pheochromocytoma is a rare form of cancer that develops in the middle part of the adrenal gland. Adrenal glands are located on top of each kidney and release hormones to regulate blood pressure and heart rate. The presence of a pheochromocytoma tumor causes an excess release of these hormones. It can occur as a single growth or as multiple growths. In severe cases, it can spread throughout the body. Patients can develop pheochromocytoma at any age, but are most common in early to mid-adulthood.
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Most people with pheochromocytoma do not develop cancer. However, untreated pheochromocytoma may cause complications, such as high blood pressure and swelling. While the symptoms will eventually go away, doctors may suggest lifelong follow-up. If you experience any of these symptoms, visit your health care provider for further treatment. If the tumor returns, call your doctor immediately.
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The primary symptoms of pheochromocytoma include high blood pressure, sweating, and palpitations. If untreated, pheochromocytoma can cause other serious health issues, such as high blood pressure, and may result in a heart attack. In addition to these symptoms, pheochromocytoma can also cause high blood pressure, headaches, anxiety, and sweating.
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Among the pheochromocytoma symptoms, high blood pressure is the most common. This can occur throughout the day, or may come and go. Symptoms may also include profuse sweating, a rapid heartbeat, and headache. Symptoms may be difficult to diagnose, but a doctor can help you understand them. If your doctor is concerned about your symptoms, he or she will recommend further tests to help determine the cause of your high blood pressure.
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