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Pheochromocytoma Symptoms - Oren Zarif - Pheochromocytoma


There are several ways to detect Pheochromocytoma symptoms. The most common way is by examining the tumor. Surgical removal is the most common treatment, but some doctors may recommend chemotherapy, radiation, or radiopharmaceutical therapy. If you do have the condition, your health care team will monitor it for signs and symptoms. Untreated pheochromocytoma can spread to the bones or cause high blood pressure or arrhythmia.

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The symptoms of Pheochromocytoma are similar to those of other types of tumors. The condition starts in specialized cells of the adrenal gland called chromaffin cells. These cells secrete catecholamines. These hormones help the body fight or flight. High blood pressure, rapid breathing, sweating, and palpitations can all be signs of Pheochromocytoma. The symptoms of this condition are similar to those of other tumors, so a doctor's attention is essential.

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During an episode, you may feel anxious, sweating, or have a headache. The duration and frequency of the attacks tend to increase with the disease, and they can last for minutes or hours. Pheochromocytoma symptoms can be triggered by trauma, drugs, or emotional trauma. Moreover, these symptoms can be triggered by simple activities such as urination. In addition, they may trigger symptoms of anxiety or depression.

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While the symptoms of pheochromocytoma overlap with those of many disorders, they stand out due to their severeness. Most patients experience high blood pressure, sweating, anxiety, and palpitations. A blood or urine test may be performed to rule out this condition if you have a hereditary syndrome. Once diagnosed, a treatment can be determined. You may have a tumor or other type of disease.

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Although high blood pressure is not a pheochromocytoma symptom, it is the most common clinical manifestation. Around 10% of patients with pheochromocytoma will have normal blood pressure. Some patients experience episodic hypertension or a rise in blood pressure. If this occurs, your doctor will want to evaluate your symptoms immediately. Those who have high blood pressure will need immediate treatment.

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Fortunately, there is no cure for pheochromocytoma, but if you suffer from the symptoms, it's important to see a doctor as soon as possible. Pheochromocytoma can be fatal, so the symptoms you experience will depend on the severity of your condition. However, genetic testing may be recommended to determine your risk. When a diagnosis is made, treatment will be tailored to your individual needs.

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Most pheochromocytomas grow within the adrenal gland's cortex, but about 10% grow outside of the gland. Because less than 10% of pheochromocytomas are cancerous, treatment is usually a surgical procedure. Surgery can result in high catecholamine levels, so the surgeon may delay surgery until the symptoms are controlled. Then, beta-blockers can control symptoms safely.

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Testing for pheochromocytoma can also be performed by a doctor. A blood test will reveal elevated levels of catecholamines, metabolites of adrenaline. Other blood and urine tests can be performed to rule out other causes of elevated levels. If there is a suspicion of genetic disease, a CT or MRI of the abdominal region may be recommended. Pheochromocytoma can be removed surgically, but it should be done only by a specialized adrenal endocrine surgeon.

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A genetic predisposition to pheochromocytoma or paraganglioma is the most common cause of the disease. It is caused by a mutated gene that is not expressed without a trigger. The mutated gene may never lead to a tumor. However, in some cases, a mutation in this gene may cause the disease. The genetic change may be passed on to children.

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