An update on Cushing syndrome in pediatrics

Abstract

Cushing syndrome (CS) in childhood results mostly from the exogenous administration of glucocorticoids; endogenous CS is a rare disease. The latter is the main reason pediatric patients with CS escape diagnosis for too long. Other barriers to optimal care of a pediatric patient with CS include improper following of the proper sequence of testing for diagnosing CS, which stems from lack of understanding of pathophysiology of the hypothalamic-pituitary-adrenal axis; lack of access to proper (i.e., experienced, state-of-the-art) surgical treatment; and unavailability of well-tolerated and effective medications to control hypercortisolemia. This report reviews the state-of-the-art in diagnosing CS and provides an update on the most recent discoveries in its genetics and treatment.

Keywords: Adrenal cancer; Adrenal cortex; Adrenocortical hyperplasia; Cancer des glandes surrénales; Carney complex; Complexe de Carney; Cortex surrénal; Cushing syndrome; Hyperplasie corticosurrénalien; Pituitary tumors; Syndrome de Cushing; Tumeurs de l’hypophyse.