Pheochromocytoma Symptoms come from a catecholamine-secreting tumor that is derived from chromaffin cells. Pheochromocytoma is benign which mean that this tumor is not cancerous, but this tumor can cause great danger to health. It can cause high blood pressure and other related symptoms. Symptoms those are common in Pheochromocytoma as palpitations, nausea, headaches, flushing of face and vomiting.
Pheochromocytoma Symptoms can occur because of single or as multiple tumors. The tumor can develop in the medulla or both adrenal glands. If you will overlook the symptoms of Pheochromocytoma, the consequences can be very disastrous or even fatal. If you are diagnose that you have this kind of illness, then it is curable especially if Pheochromocytoma it is detected earlier.
Pheochromocytoma Symptoms – a hereditary illness
If you have Pheochromocytoma Symptoms, your adrenal gland will produce excess hormones that can raise your blood pressure and heart rate. Pheochromocytoma starts in the adrenal gland or in the medulla adrenal where chromaffin cells are situated.
Actually, there are two adrenal glands, the first one is located just above the kidney and the one can be found at the upper part of the abdomen. Pheochromocytoma is a disease that can be inherited, because according to studies 10% of patient who suffered from Pheochromocytoma has a family member who also experienced the same illness in the past. Familial cases usually happen in younger patients.
Pheochromocytoma symptoms are experienced by patients, because the adrenal gland excretes too many hormones known as catecholamines. The treatment of this illness can lead to normal blood pressure after successfully treating the disease.
This is the reason why patients experiencing Pheochromocytoma symptoms should immediately consult a doctor for further diagnosis and possible treatments. Pheochromocytoma is usually detected from young to middle aged adults with ages 30 to 60 years up. This tumor can be found in almost all parts of the body, though the tumor usually occurs in the adrenal medulla.
Even if you are just suffering from very tiny Pheochromocytoma, it can cause a person to experience uncontrollable Pheochromocytoma symptoms. There are patient who developed Pheochromocytoma have a very rare health condition that is called multiple endocrine neoplasia.
This disease makes them prone to tumor growth in parathyroid thyroid and adrenal glands. There are only few cases that a Pheochromocytoma becomes malignant. Pheochromocytoma can be life threatening if you overlooked possible treatments.
The Most Common Pheochromocytoma Symptoms
The most common Pheochromocytoma symptoms are severe headache, excess sweating, nervousness, palpitations, abdominal pain, severe weight loss, Hypertensive retinopathy and anxiety. There are several methods that can be used in order to treat Pheochromocytoma.
It is important to stabilize the vital signs of the patient with proper medications and surgery can treat Pheochromocytoma. If you are suffering from uncontrollable and intolerable symptoms hospitalization is badly needed by the patient.
Surgery is the most common way to treat Pheochromocytoma. The tumor will be removed and the blood pressure will normalize again right after the surgery. Patients can also take Alpha blocker that is also known as alpha-adrenergic blocking agents. It can help in relaxing muscles and can aid small blood vessels to remain open to prevent vasoconstriction.