While the exact symptoms of pheochromocytoma vary from patient to patient, they're often quite similar to other conditions. Most patients experience high blood pressure, but not all people experience this complication. In addition, episodes of pheochromocytoma can occur at any time. In some cases, it can be triggered by certain life events or foods. For instance, consuming tyramine, a chemical found in aged or fermented foods and chocolate, can trigger an episode. Additionally, a certain class of medications known as monoamine oxidase inhibitors may trigger symptoms of pheochromocytoma.
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If an imaging examination shows adrenal nodules, a biochemical workup will be ordered. In this way, your doctor will be able to determine if the nodule is producing excessive levels of noradrenaline and adrenaline. MRIs will also provide a diagnosis of pheochromocytomas and determine their severity. While they may appear similar, pheochromocytomas will display distinctive imaging characteristics.
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Acute respiratory distress syndrome is a rare complication of pheochromocytomas, which is associated with increased heart rate, breathing difficulty, and hypotension. Another rare complication is an acute abdominal catastrophe, which is marked by pain, fluctuating blood pressure, and high or low blood pressure. These complications can affect any organ system, including the heart. In severe cases, the condition can result in pulmonary edema and heart failure.
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Although most pheochromocytomas are incidental tumors, the majority of patients exhibit a range of symptoms. Patients with incidentalomas, asymptomatic pheochromocytomas may have no symptoms at all. The triad is only present in a minority of incidental cases. This disease is often diagnosed late because of a lack of imaging. Nonetheless, pheochromocytomas can be life-threatening if detected early.
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Another symptom of pheochromocytoma is high blood pressure. Interestingly, only 10% of patients with pheochromocytoma have normal blood pressure. People with normal blood pressure also frequently experience episodes of high blood pressure. These episodes of high blood pressure may not be indicative of pheochromocytoma, but they should raise suspicions. The symptoms of pheochromocytoma vary from person to patient, so you should consult your doctor if you experience any of these conditions.
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When a patient experiences these symptoms, their doctor will most likely perform additional tests to confirm the diagnosis. Some common symptoms of pheochromocytoma include high blood pressure, sweating, anxiety, and palpitations. If left untreated, pheochromocytoma can lead to serious health problems, such as heart disease or stroke. A doctor will measure the catecholamine levels in the blood and will likely order imaging tests to find the tumor.
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Because pheochromocytomas are neuroendocrine tumors, their clinical signs include high blood pressure, heart palpitations, and other similar conditions. Most pheochromocytomas are treatable, and most are curable with targeted surgery. However, some patients may require chemotherapy or radiation. The best treatment for pheochromocytoma is a surgical procedure that targets these cells.
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If you notice these symptoms after surgery, you should contact your health care provider. The tumor may be benign or cancerous. In the latter case, it may grow back after the operation. In such cases, pheochromocytoma patients need to undergo follow-up exams to monitor for its return. In the majority of cases, the condition does not return to its original status. Your doctor may want to follow up with you for life to make sure the treatment is going well.
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The most common symptom of pheochromocytoma is high blood pressure. Most people suffering from this condition do not have this condition, but they may experience high blood pressure and heavy sweating. These symptoms are common and should be taken seriously. If you have any of these symptoms, make an appointment with your doctor to get a proper diagnosis. And remember, there is no cure for pheochromocytoma, so you'll have to wait to know if you have a pheochromocytoma.
