Although the most common symptom of pheochromocytoma is palpitations, the other possible symptoms include sweating, headaches, and anxiety. In fact, nearly one-fifth of the patients had all three of these symptoms at some point. Acute and chronic releases of catecholamines can lead to complications. These can affect any organ system. In rare cases, a patient can develop a heart rhythm abnormality, pulmonary edema, or even a heart failure.
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Blood and urine tests will help confirm the diagnosis of pheochromocytoma. Urine testing can determine whether or not the adrenal nodule is producing excessive hormones. Blood tests may also confirm the presence of a tumor, while imaging tests may reveal whether a patient is suffering from a hereditary syndrome. Early detection is crucial to preventing complications and minimizing the risk of the tumor returning.
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A patient suffering from this condition will also experience symptoms like high blood pressure and sweating. The tumor grows in the center of the adrenal glands, which secretes hormones that regulate blood pressure and fluid metabolism. This causes high blood pressure and increased levels of catecholamines. This causes excessive production of these hormones and damages the cardiovascular system. Therefore, it is critical to seek a diagnosis immediately.
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Although pheochromocytoma symptoms usually go away after the tumour has been removed, some people may experience recurrence of symptoms in some months or years. Symptoms should be reported to your GP as soon as possible, so that your symptoms can be monitored as needed. For more information on pheochromocytoma, visit the Cancer Research UK website.
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High blood pressure is the most common symptom of pheochromocytoma, but patients may also experience episodic hypertension or constant high blood pressure. High blood pressure may cause headaches and heart palpitations, or it may cause sweating and tremors. A patient with pheochromocytoma may also experience high blood pressure, which can lead to a heart attack or a stroke.
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Surgical removal of the tumor is the most effective treatment for pheochromocytoma. However, surgery is delayed until the release of catecholamines is under control. Otherwise, the tumor may cause complications during surgery, which is not safe for patients. Besides, phenoxybenzamine may be prescribed to control the effects of the hormone, and beta-blockers may be used to safely control the symptoms after surgery.
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High blood pressure is the most common symptom of a pheochromocytoma, although this symptom is associated with a wide variety of other conditions. High blood pressure is one of the most common pheochromocytoma symptoms, as it can lead to a heart attack, stroke, or even death. Symptoms can be difficult to detect, but if they persist, a doctor may perform a series of tests to determine a diagnosis.
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Other pheochromocytomas are extra-adrenal and occur outside of the adrenal gland. People of any age can develop pheochromocytoma, although their incidence is highest between the third and fifth decades of life. Pheochromocytomas are relatively rare and most cases are benign. However, high blood pressure may result in complications and lead to symptoms.
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When diagnosing a pheochromocytoma, it is crucial to consider the potential asymptomatic and symptomatic manifestations of the disease. Because pheochromocytomas are relatively uncommon and typically present without the classic triad, early detection is critical. For this reason, a patient with a suspected pheochromocytoma must undergo a full evaluation by a physician.
