People who suffer from pheochromocytoma should be aware of the symptoms of the disease, such as abdominal pain, sweating, and difficulty breathing. These symptoms may be the result of a neuroendocrine tumor, which releases too many catecholamines into the bloodstream. These symptoms may last minutes, hours, or days, and they may be indicative of a different medical condition.
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High blood pressure is a common symptom, though it is not the only one. People with pheochromocytoma can suffer from both chronic and intermittent episodes of high blood pressure. The patient may also experience heart palpitations, sweating, or anxiety. These symptoms can be sporadic, or they can be more frequent and severe as the tumor grows. The patient should seek medical attention if they experience any of these symptoms.
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High blood pressure is one of the most common pheochromocytomas symptom. While most people with this condition have high blood pressure, most of them do not have this disease. High blood pressure can also be associated with headaches, a rapid heart rate, and heavy sweating. If you experience any of these symptoms, talk to your doctor, who will determine if you have a pheochromocytoma or other conditions.
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A blood catecholamine study may be performed to confirm the diagnosis of pheochromocytoma. Catecholamines are hormones that are released into the blood, and the breakdown of these chemicals produces substances. Abnormal levels of catecholamines indicate a disease in an organ or tissue. When these substances are present in large amounts in the blood, pheochromocytoma is most likely to be the cause of the symptoms.
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Genetic disruptions are the cause of 35% of cases of pheochromocytoma. These disorders are inherited in the autosomal dominant pattern. This means that each individual inherits one copy of an altered gene from either parent or have it introduced through a mutation. In either case, the risk of passing the gene is 50 percent. Therefore, genetic screening is recommended for those with a family history of pheochromocytoma.
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Atypical pheochromocytoma can present with a variety of symptoms, but a majority of patients have incidentalomas, and therefore no classic triad. A patient's symptoms should be evaluated by a physician to rule out incidentalomas. The earliest possible diagnosis is life-saving. If a diagnosis is delayed, it may result in an unnecessary and costly surgery.
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Among the symptoms of pheochromocytoma are high blood pressure and persistent vomiting. These are common symptoms of pheochromocytoma. However, they are not necessarily indicative of pheochromocytoma. A doctor will assess the cause and symptoms of pheochromocytoma. They may also suggest treatments. In some cases, surgery is necessary to remove the tumor.
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If your doctor has diagnosed pheochromocytoma, they may recommend surgery. Chemotherapy can be helpful, but it does not cure the condition. However, the latest chemotherapy drugs are more targeted and can slow down the growth of the tumor. Radioisotopes can also be used to target the affected tissues. Beta-blockers, doxazosin, and phenoxybenzamine are some of the medicines that block the harmful effects of excessive catecholamines.
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People with pheochromocytoma have elevated blood pressure and other symptoms associated with the disease. Pheochromocytoma is a rare form of adrenal gland tumor that affects both adrenal glands. Because it affects the production of catecholamine hormones, it can lead to high blood pressure and other health problems. However, it is important to note that pheochromocytoma is usually benign, though it can be cancerous. In around three to thirteen percent of cases, pheochromocytoma becomes cancerous, and in those cases, it can spread to other parts of the body.
