#pheochromocytoma, #tumor, #adrenalglands, #cancer
Pheochromocytoma is a rare type of tumor that develops in the adrenal glands. The adrenal glands are two small glands that sit on top of the kidneys. They produce hormones that help regulate the body’s blood pressure, blood sugar, and other functions.
Pheochromocytomas can be either benign (non-cancerous) or malignant (cancerous). They can also be either sporadic (occurs for no known reason) or inherited.
The symptoms of pheochromocytoma can vary depending on the size and location of the tumor. Some common symptoms include:
High blood pressure
Headaches
Sweating
Palpitations
Anxiety
Nausea and vomiting
Weight loss
Flushing
Fever
If you experience any of these symptoms, it is important to see a doctor right away. Pheochromocytomas can be life-threatening if they are not treated.
The treatment for pheochromocytoma depends on the size and location of the tumor, as well as whether it is benign or malignant. In most cases, the tumor can be removed surgically. If the tumor is malignant, chemotherapy or radiation therapy may also be used.
With treatment, most people with pheochromocytoma can live a normal life. However, it is important to continue to see a doctor regularly to monitor the tumor and make sure it does not recur.
Keywords: pheochromocytoma, tumor, adrenal glands, cancer, health, wellness, symptoms, causes, treatments, diagnosis, prognosis, surgery, chemotherapy, radiation therapy
