COEXISTING PRIMARY EMPTY SELLA SYNDROME AND ACROMEGALY
- 1 September 1977
- journal article
- research article
- Published by Wiley in Clinical Endocrinology
- Vol. 7 (3) , 261-263
- https://doi.org/10.1111/j.1365-2265.1977.tb01323.x
Abstract
The empty sella syndrome is now a more frequent diagnosis due to the increased use of pneumoencephalography in the evaluation of the enlarged pituitary fossa. This syndrome has also been classified into a primary form in which there has been no prior pituitary irradiation or surgery, and a secondary form in which the empty sella is found after such procedures. Most patients with the primary empty sella syndrome are found to have normal pituitary function while about 30% have varying degrees of hypopituitarism. It is not widely appreciated that the primary empty sella may harbor a pituitary tumor with resultant acromegaly. In this report 2 such patients are described who presented with active acromegaly. This entity of pituitary tumor in a primary empty sella merits careful consideration since the coexistence of these 2 findings may influence the therapeutic approach that might otherwise be appropriate for the pituitary tumor.This publication has 4 references indexed in Scilit:
- CO-EXISTING PITUITARY ADENOMA AND INTRASELLAR ARACHNOID INVAGINATIONAmerican Journal of Roentgenology, 1974
- THE PRIMARY EMPTY SELLAMedicine, 1973
- The Enlarged Sella and the Intrasellar CisternRadiology, 1969
- Endocrine studies in patients with the "empty sella syndrome"Archives of internal medicine (1960), 1969