Pheochromocytoma
- 16 February 1950
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 242 (7) , 252-257
- https://doi.org/10.1056/nejm195002162420705
Abstract
PHEOCHROMOCYTOMAS are rare tumors that may cause any known form of hypertension. Although the hypertension may be and most commonly is paroxysmal, it may also be nonparoxysmal. In either case, the hypertension may be intermittent or persistent. Pheochromocytomas develop from chromaffin tissue and consequently are found wherever this occurs. The most common location is the medullary portion of the adrenal gland. Tumors also arise from sympathetic-ganglion tissue and consequently may be found in various locations. The most common site of origin other than the adrenal gland is the organ of Zuckerkandl, which is located just above the aortic bifurcation. In . . .Keywords
This publication has 11 references indexed in Scilit:
- The Surgical Physiology of HypertensionSurgical Clinics of North America, 1949
- Pheochromocytoma with diabetes and hypertensionThe American Journal of Medicine, 1949
- THE USE OF TETRAETHYLAMMONIUM BROMIDE AS A DIAGNOSTIC TEST FOR PHEOCHROMOCYTOMAAnnals of Internal Medicine, 1948
- Pheochromocytoma: Report of a case, with a new diagnostic testThe American Journal of Medicine, 1948
- NEW TEST FOR HYPERTENSION DUE TO CIRCULATING EPINEPHRINEJAMA, 1947
- A TENTATIVE TEST FOR PHEOCHROMOCYTOMAThe Lancet Healthy Longevity, 1945
- ADRENAL-SYMPATHETIC SYNDROME: CHROMAFFIN TISSUE TUMOUR WITH PAROXYSMAL HYPERTENSIONHeart, 1944
- The peripheral blood flow in a case of adrenal pheochromocytoma before and after operationAmerican Heart Journal, 1942
- Tumor of Medulla of Adrenal. (Adrenal Pheochromocytoma) with Removal and Relief of Paroxysmal HypertensionJournal of Urology, 1938
- A SYNDROME DIENCEPHALIC STIMULATION OCCURRING IN PATIENTS WITH ESSENTIAL HYPERTENSIONThe Lancet Healthy Longevity, 1935