New England Journal of Medicine · 1950 · 147 citations · 10 references
MedicineEndocrinologySurgeryAnesthesiaEndocrine SurgeryNeuroendocrinologyAdrenal DisordersAdrenal EndocrinologyAdrenal SurgeryAdrenal TumorsHypertension ManagementPheochromocytoma SurgeryComplications Of AdrenalectomyIntraoperative Anesthetic ManagementOperative MorbidityOperative TreatmentPerioperative Anesthetic ManagementPheochromocytoma DiagnosisPheochromocytoma Pathology
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 . . .
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A TENTATIVE TEST FOR PHEOCHROMOCYTOMA
Grace M. Roth, Walter F. Kvale · The American Journal of the Medical Sciences · 1945 · 183 citations
Medicine, Endocrinology, Neurology +11
ADRENAL-SYMPATHETIC SYNDROME: CHROMAFFIN TISSUE TUMOUR WITH PAROXYSMAL HYPERTENSION
Ronald Mackeith · Heart · 1944 · 98 citations · Full text
Medicine, Endocrinology, Pathology +12
TREATMENT OF A PATIENT WITH A PHEOCHROMOCYTOMA
K. S. Grimson · Journal of the American Medical Association · 1949 · 82 citations
Medicine, Endocrinology, Surgery +12