Acromegaly, hyperparathyroidism, and pheochromocytoma in the same patient. A multiple endocrine disorder
- 1 October 1981
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of internal medicine (1960)
- Vol. 141 (11) , 1521-1522
- https://doi.org/10.1001/archinte.141.11.1521
Abstract
In the course of follow-up of a patient with primary hyperparathyroidism, signs and symptoms of acromegaly developed. The patient subsequently was found to have recurrent primary hyperparathyroidism and, later, pheochromocytoma was discovered. The patient seems to have an overlap of features found in the multiple endocrine neoplasia syndromes, type 1 and type 2 as previously classified.This publication has 2 references indexed in Scilit:
- Parathyroid Function in Patients with PheochromocytomaAnnals of Internal Medicine, 1975
- A review of 17 cases of carcinoma of the thyroid and phaeochromocytomaJournal of Clinical Pathology, 1965