Pheochromocytoma occurs in the Nervous System and in the Adrenal Gland.
Pheochromocytoma is a rare tumor of the adrenal glands that produces adrenaline. There are approximately 1,000 new cases of pheochromocytoma tumors in the United States each year.
The adrenal gland
If a pheochromocytoma is suspected, urine and/or a blood test are usually recommended. A test called "24-hour urinary catacholamines and metanephrines" will be done.
Localized benign pheochromocytoma means that the tumor is found only in one area, is not cancer, and cannot spread to other tissues of the body
means that a malignant tumor that was removed has come back
Any test can be a false negative.
cathecolamines producing vasoconstriction, causing pallor.
to prevent the leakage of epinephrine during the surgery
this is a scan for pheochromocytoma; MIBG stands for metaiodobenzylguanidine.
I believe the term you are looking for is pheochromocytoma. It is an adrenal cell tumor that causes the pulsatile secretion of catecholamines. So basically these people will occasionally have a rush of adrenaline causing a high blood pressure, high pulse rate, and a feeling of impending doom, among other symptoms.
Propanolol is a non-selective beta 1 and beta 2 receptor antagonist. When it is used in the treatment of pheochromocytoma, there is continued activation of the alpha 1 receptors leading to a paradoxical rise in hypertension due to the loss of vasodilatory affects inherent in beta 2 adrenergic stimulation. Case reports and reviews also show an increased incidence of pulmonary edema resultant from use of Propanolol in pheochromocytoma