| Literature DB >> 6096999 |
J Lamovec, V A Memoli, J A Terzakis, S C Sommers, V E Gould.
Abstract
A 42-year-old female with clinical and endocrine indications of Cushing's syndrome, as well as periodic hypertension and increased urinary catecholamines and their metabolites, benefitted from removal of a pheochromocytoma. Adrenocortical hyperplasia was present. Electron microscopy showed catecholamine-type granules in the tumor cells; in addition, immunoreactive ACTH, leu-enkephalin, somatostatin, and serotonin were identified. Such studies were performed for the first time in this unusual condition.Entities:
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Year: 1984 PMID： 6096999 DOI： 10.3109/01913128409141852
Source DB: PubMed Journal: Ultrastruct Pathol ISSN： 0191-3123 Impact factor: 1.094