Progress, challenges and perspectives in the management of hypopituitarism.
Rev Endocr Metab Disord
; 25(3): 453-455, 2024 Jun.
Article
in En
| MEDLINE
| ID: mdl-38801648
ABSTRACT
Hypopituitarism is a rare endocrine disorder characterized by insufficient hormone secretion from the pituitary gland. This condition leads to deficient production of one or more pituitary hormones, including growth hormone (GH), thyroid-stimulating hormone (TSH), luteinizing hormone (LH), follicle-stimulating hormone (FSH), adrenocorticotropic hormone (ACTH), and antidiuretic hormone (ADH), also called arginine vasopressin (AVP). Symptoms vary widely and are often not, late recognized.Diagnosis typically involves a thorough clinical evaluation, hormone level assessments, and neuroimaging studies to identify underlying causes. Treatment aims to replace deficient hormones and address the underlying cause and related complications when possible. In this special issue we address diagnosis, comorbidities, and management of hypopituitarism. We hope that it will help healthcare professionals to manage their patients.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Hypopituitarism
Limits:
Humans
Language:
En
Journal:
Rev Endocr Metab Disord
Journal subject:
ENDOCRINOLOGIA
/
METABOLISMO
Year:
2024
Document type:
Article
Affiliation country: