Although phaeochromocytomas are not always curable, they can be controlled with medication. If they are not caught early, they can lead to serious health problems, including irregular heartbeat, heart attacks, strokes, and organ failure. While most pheochromocytomas can be removed with surgery, they may return in a small number of people. Nevertheless, regular check-ups and monitoring are necessary to detect and treat the condition.
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One of the most common pheochromocytoma symptoms is an increased blood pressure. Elevated systolic blood pressure is the most common clinical manifestation. This symptom occurs randomly and is not associated with any specific trigger or catecholamine surge. Pheochromocytoma patients typically experience elevated blood pressure, which is resistant to traditional treatment regimens and threatens end-organ damage. Treatment must begin immediately if a patient experiences a life-threatening hypertensive episode.
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Associated with high blood pressure, a patient may experience chest pain, or even a pounding heartbeat. Atypical pheochromocytoma symptoms may include abnormally high blood pressure or heavy sweating. Patients may also experience abnormal heart rhythms or abdominal pain. Pheochromocytoma symptoms may include chest pain, nausea, or abdominal pain. Pheochromocytoma can lead to congestive heart failure and cardiac hypertrophy.
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Patients with isolated pheochromocytoma/paraganglioma may have a genetic predisposition. This predisposition is associated with a mutated gene. If this gene is expressed without a trigger, a tumor will not develop. Some cases result from a spontaneous genetic change, which can be passed to children. In these cases, genetic testing should be done.
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Some pheochromocytoma symptoms are not immediately noticeable. However, high blood pressure is the most common symptom. It may be present all the time, or occur during episodes. This condition may also cause excessive sweating and headache. High blood pressure can be life-threatening if undiagnosed, and it is recommended to see a doctor to rule out other conditions. There are some ways to manage these symptoms, however.
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Pheochromocytomas can mimic many other conditions, and the symptoms vary between patients. Although they commonly present with headaches, tremor, and sweating, some can be detected without symptoms. Pheochromocytomas can be a difficult tumor to diagnose, and doctors should be aware of any unusual changes in your body. They may be difficult to detect, but the good news is that they can be detected early and treated effectively.
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The genetics of pheochromocytoma may run in families. Between 25 and 35% of cases are inherited. Genetic conditions such as neurofibromatosis have been linked to this disease. Scientists have found mutations in twenty genes that may be associated with pheochromocytoma and paraganglioma. However, they have not been proven to cause pheochromocytoma.
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While the onset of symptoms is based on the clinical presentation, some patients may be safely discharged without undergoing surgery. The current study found that some patients may be safely discharged if the tumor is small and localized. However, the findings suggest that more research is necessary. Therefore, a comprehensive diagnostic evaluation is essential. And, if you suspect pheochromocytoma, contact a doctor.
