Abstract:Nelson’s syndrome nowadays a rare entity results from an adrenocorticotropin (ACTH)–secreting pituitary adenoma in patients with refractory Cushing's disease after a therapeutic bilateral adrenal gland removal. We report a case of 25 year old female with cushing’s disease who was initially managed with medical treatment, but in view of severe persistent hyper cortisol state was subjected to bilateral adrenalectomy following which she developed Nelson’s syndrome after a gap of six years, which was difficult to … Show more
“…Los síntomas son: hiperpigmentación de la piel, mucosas y membranas, cefalea, diabetes insípida, panhipopituitarismo, dolor testicular y oligospermia. La forma de diagnóstico es el control de los niveles de ACTH (20).…”
“…Los síntomas son: hiperpigmentación de la piel, mucosas y membranas, cefalea, diabetes insípida, panhipopituitarismo, dolor testicular y oligospermia. La forma de diagnóstico es el control de los niveles de ACTH (20).…”
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.