Symptoms of pheochromocytoma usually include headache, sweating, and a rapid or irregular heartbeat. However, pheochromocytoma can also cause a variety of other symptoms, including anxiety, palpitations, and stomach pain. Although the symptoms of pheochromocytoma can often be difficult to detect, it is important to seek medical attention if you are experiencing any of these.
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Most pheochromocytoma patients can expect ongoing follow-up for a few years after their surgery to monitor the condition and monitor the progress of the disease. These follow-ups will include periodic urine or plasma tests to check for recurrences. Patients will need to undergo regular follow-ups throughout their treatment, but they are typically not required to undergo a follow-up CT or MRI after the surgery.
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High blood pressure is the most common symptom of pheochromocytoma. While the majority of pheochromocytoma patients experience high blood pressure, about 10% have normal blood pressure. High blood pressure may occur permanently or occasionally, called episodic hypertension. Although asymptomatic high blood pressure is common, it should raise suspicions. In rare cases, the patient may also experience vomiting, fatigue, and gastrointestinal distress.
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Some pheochromocytomas are asymptomatic, but high blood pressure is often a sign of a developing tumor. High blood pressure is associated with headaches, sweating, and a rapid heartbeat. The tumor may also produce excessive amounts of epinephrine, or catecholamines, which increase blood pressure. These hormones are essential for human life, and can cause symptoms of hypertension.
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Although pheochromocytomas present with a variety of symptoms, they are most common among incidentalomas. As a result, incidentalomas have a greater likelihood of presenting with symptoms than screened patients. In addition to hypertension, incidentalomas are often accompanied by other illnesses, including strokes, cardiac problems, and kidney cancer. Therefore, early detection is vital in preventing death and suffering from other complications related to this rare disease.
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If you suspect you might have pheochromocytoma, it's important to schedule a consultation with your doctor. Your doctor will evaluate your symptoms and suggest a course of treatment. The most common treatments for pheochromocytoma include surgery and chemotherapy. While you should seek medical advice if you notice any of these symptoms. Your doctor will also perform imaging tests to determine the tumor's location.
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While pheochromocytoma is a benign tumor, it can also be cancerous in around three to thirteen percent of cases. While pheochromocytoma is usually not life threatening, cancerous pheochromocytomas can spread to other areas of the body. For this reason, it is important to seek medical care early and regularly. If you notice any of these symptoms, consult your doctor right away to ensure that you have a full understanding of your condition and how to treat it.
