High blood pressure is one of the most common symptoms of pheochromocytoma, but it is not the only one. In fact, high blood pressure can be life-threatening. Pheochromocytoma symptoms can be hard to identify because they may look similar to other health issues. Blood tests and urine analysis are important to diagnose pheochromocytoma, and other diagnostic tests can be performed. CT scans and MRIs are diagnostic tests that use computer technology to take detailed images of the body.
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Patients with pheochromocytoma may experience episodes that occur frequently or only occasionally. Paroxysms can last minutes or several hours. They tend to increase in frequency and duration over time. Some people experience high blood pressure in a paroxysm. If you experience any of these symptoms, it is best to see your doctor as soon as possible. The symptoms of pheochromocytoma can be frightening and life-threatening.
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Among pheochromocytoma, high blood pressure is one of the most common signs. Only 10% of people with the disease have normal blood pressure. However, the symptoms of hypertension are often more severe than other conditions. While high blood pressure is not the only sign of pheochromocytoma, it should raise a patient's suspicions. If a person is experiencing high blood pressure in addition to the other symptoms, they should contact their doctor immediately.
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Urine and blood tests can reveal abnormal levels of adrenaline and noradrenaline. Imaging tests can confirm the presence of a pheochromocytoma. Pheochromocytomas have characteristic appearance on imaging tests. Genetic testing is also useful in identifying a gene mutation that increases the risk of developing the condition. During a routine checkup, your doctor may recommend genetic testing for relatives. Pheochromocytoma treatment usually involves surgical removal of the tumor.
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In addition to chest pain, patients with pheochromocytomas may experience symptoms related to poor blood flow to the heart, including cardiac ischemia. They may develop congestive heart failure or hemorrhagic infarction. In some cases, pheochromocytomas present as incidental findings on cross-sectional imaging. The symptoms of pheochromocytomas vary widely between the two types.
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While pheochromocytoma is rarely fatal, if left untreated, it can lead to serious complications. While the symptoms are usually temporary, doctors may recommend lifelong follow up to monitor the tumor's growth. However, it is important to note that the symptoms of pheochromocytoma can vary from person to person and may be due to other medical conditions.
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If your thyroid and adrenal glands have undergone imaging, you should get biochemical workup to determine whether there's an overproduction of catecholamines. These hormones control heart rate, blood pressure, and blood sugar. Pheochromocytoma is a rare and serious disease. The symptoms of pheochromocytoma can be life-threatening. There's no cure yet, but there is hope.
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Treatment of pheochromocytoma includes surgery to remove the tumor. The operation is performed with an alpha-blocker to keep vital signs, including blood pressure and heart rate, stable. This will help prevent serious complications during surgery. Because the surgery involves manipulating the tumor, the surgeon may have to release hormones that raise blood pressure and heart rate. Therefore, the doctor should have experience in performing this procedure and should be experienced in the procedure.
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The symptoms of pheochromocytoma include high blood pressure, sweating, and rapid breathing. The condition can also cause high blood pressure and can be associated with anxiety. If you experience any of these symptoms, you should visit a doctor immediately. The most common symptom of pheochromocytoma is high blood pressure. However, once the tumor has been removed, the condition will no longer be a problem.
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The most common pheochromocytoma symptoms are headache, high blood pressure, and heavy sweating. Despite the fact that pheochromocytomas are extremely rare, many people go undiagnosed for their entire lives. Most of them are benign and non-cancerous. However, because they share similar symptoms with other disorders, comparisons may help in the differential diagnosis.
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Metastatic pheochromocytoma has no cure, but existing treatments can help reduce tumors and prolong life. The prognosis of metastatic pheo is largely dependent on the size of the primary tumor, and the level of methoxytyramine in the blood. It can be genetically predisposed to metastatic pheo. Metastatic pheo can spread to bones, lymph nodes, and the liver.
