When diagnosed, patients may experience the following Pheochromocytoma symptom patterns: high blood pressure, sweating, and anxiety. However, these symptoms may not be present in every patient. For example, a person with a hereditary syndrome may have high blood pressure, but this symptom pattern is not always indicative of pheochromocytoma. The presence of any of these symptoms should raise a person's suspicion about pheochromocytoma.
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There are some other possible complications associated with pheochromocytoma. One of these is acute respiratory distress syndrome, which is characterized by extreme blood pressure and adrenaline release from the tumor. Another complication is acute abdominal catastrophe, which is characterized by severe pain, high blood pressure, and fluctuating blood pressure. While both of these complication types are uncommon, these symptoms should be considered.
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Treatment for pheochromocytoma usually involves surgery. Chemotherapy is rarely successful in curing this condition. However, newer drugs can slow tumor growth and radioisotopes may target specific areas of the tumor. Other medications, such as doxazosin, phenoxybenzamine, and beta-blockers, can block the toxic effects of excess catecholamines.
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While the majority of PCC tumors are benign, many of them can lead to serious complications if left untreated. In most cases, the symptoms will disappear once the tumor is removed, but doctors may recommend routine follow-ups to check for recurrence. The only way to tell if pheochromocytoma has returned is to get it diagnosed and treated. The treatment options will depend on the type of PCC you have, but your doctor will help you decide which treatments are right for you.
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The most common pheochromocytoma symptom is high blood pressure. High blood pressure can be life-threatening if pheochromocytoma is untreated. Pheochromocytoma symptoms can mimic other health conditions. Your doctor will conduct a number of tests, such as blood pressure and urine analysis. If your doctor suspects the cancer is familial, genetic tests will be performed.
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A blood catecholamine study will measure the amount of catecholamines in your blood and any substances released from its breakdown. A high level of certain catecholamines is indicative of pheochromocytoma. Pheochromocytoma symptoms may be accompanied by other symptoms, such as fever, sweating, and paroxysmal hypertension. If you are concerned about genetics, genetic counseling can help you understand your condition.
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Unlike other forms of cancer, pheochromocytoma is an uncommon form of tumor that grows inside of an adrenal gland. Adrenal glands have two layers. Each layer produces different hormones. The middle gland produces epinephrine and noradrenaline, which help regulate your body's heart rate. Pheochromocytoma tumors cause the release of too much norepinephrine, causing a rise in your blood pressure.
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The most common symptom of pheochromocytoma is high blood pressure. However, this condition may be accompanied by other symptoms, including high blood pressure, sweating, and a rapid heartbeat. A physician will likely ask you about your symptoms and make a diagnosis based on them. The symptoms of pheochromocytoma are usually very similar to those of other cancers, so your doctor will want to make a differential diagnosis before deciding on the cause of your pain.
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The clinical signs of pheochromocytoma depend on where the tumor is located. The adrenal gland produces hormones called catecholamines that control the body's response to stress and other factors. A pheochromocytoma in the adrenal gland is a tumor of the catecholamine-secreting cells. This type of cancer is rare, but it can affect people of all ages. The hormones released by this type of tumor can damage the heart, the brain, and lungs.
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A thorough clinical evaluation and detailed patient history can suggest pheochromocytoma. Blood and urine analysis can also confirm a diagnosis. In some cases, high blood pressure is present during the passage of urine or when the patient has undergone surgery to remove the tumor. Although there are no known causes of pheochromocytoma, these symptoms may occur as a result of a hereditary paraganglioma.
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People with Pheochromocytoma often experience excessive sweating and high blood pressure. These symptoms can also be accompanied by sweating and anxiety, and can even lead to death if not detected in time. Pheochromocytoma symptoms are similar to those of other conditions, so the symptom severity is a good indicator of the disease's presence. For more information on these symptoms, visit a doctor or adrenal gland specialist.
