Abstract
Rationale:
Due to the proximity of craniopharyngiomas to the hypothalamus and pituitary gland, most children and adolescents presenting with these tumors will exhibit significant endocrine dysfunction. After treatment, these impairments can become a major cause of morbidity and mortality.
Methods:
The postoperative course of children undergoing surgery for craniopharyngioma is reviewed.
Conclusion:
Even if hormone levels seem to be adequate in the short term after treatment, deficiencies may develop over years and need to be monitored closely.
MeSH terms
-
Adrenocorticotropic Hormone / deficiency
-
Body Weight / physiology
-
Child
-
Child, Preschool
-
Craniopharyngioma / physiopathology*
-
Craniopharyngioma / surgery
-
Endocrine System / physiopathology*
-
Endocrine System Diseases / etiology*
-
Follicle Stimulating Hormone / deficiency
-
Humans
-
Luteinizing Hormone / deficiency
-
Neurophysins / metabolism
-
Pituitary Neoplasms / physiopathology*
-
Pituitary Neoplasms / surgery
-
Postoperative Complications*
-
Protein Precursors / metabolism
-
Thyrotropin / metabolism
-
Vasopressins / metabolism
Substances
-
AVP protein, human
-
Neurophysins
-
Protein Precursors
-
Vasopressins
-
Adrenocorticotropic Hormone
-
Luteinizing Hormone
-
Follicle Stimulating Hormone
-
Thyrotropin