Chemical Determination of Urinary Catecholamines
- 1 August 1957
- journal article
- research article
- Published by American Medical Association (AMA) in A.M.A. Archives of Internal Medicine
- Vol. 100 (2) , 196-200
- https://doi.org/10.1001/archinte.1957.00260080022006
Abstract
The classical description of patients with pheochromocytoma includes, as typical symptoms, paroxysmal hypertension, pallor, sweating, and tachycardia. It is now known that only a minority of patients exhibit such symptoms.1,2The majority of cases manifest only a persistent hypertension and are difficult to differentiate from cases of essential hypertension. The proportion of pheochromocytomas among cases of hypertension, while small, is significant. Graham3encountered 8 cases, or 0.47%, of pheochromocytoma among 1700 unselected patients with hypertension subjected to bilateral lumbodorsal splanchnicectomy. If this percentage is correct, approximately 1 out of every 200 cases of hypertension involves a pheochromocytoma. It thus becomes important to have a highly specific method for the diagnosis of the latter disease. The pharmacologic tests, such as the histamine, benzodioxane, and phentolamine (Regitine) tests, are known to yield both false-negative and false-positive tests.1,4,5Since Engel and von Euler6first pointed out in 1950 theThis publication has 0 references indexed in Scilit: