Pheochromocytoma? - Answers

What is a pheochromocytoma?

A pheochromocytoma is a rare tumor that develops in the adrenal glands. These glands are located on top of each kidney and produce hormones such as adrenaline and noradrenaline. Pheochromocytomas can cause high blood pressure, headaches, sweating, and palpitations.

What are the symptoms of a pheochromocytoma?

The symptoms of a pheochromocytoma can vary depending on the size and location of the tumor. Some common symptoms include:

* High blood pressure

* Headaches

* Sweating

* Palpitations

* Anxiety

* Tremors

* Weight loss

* Nausea and vomiting

How is a pheochromocytoma diagnosed?

A pheochromocytoma is diagnosed based on the patient's symptoms and a physical examination. The doctor may also order blood and urine tests to measure the levels of hormones produced by the adrenal glands. Imaging tests, such as a CT scan or MRI, may also be used to identify the tumor.

How is a pheochromocytoma treated?

The treatment of a pheochromocytoma typically involves surgery to remove the tumor. In some cases, medication may be used to control the symptoms of the tumor before surgery.

What is the prognosis for a pheochromocytoma?

The prognosis for a pheochromocytoma is generally good. Most patients who have surgery to remove the tumor are able to live a normal life. However, the prognosis may be less favorable for patients with a malignant pheochromocytoma.