Craniopharyngioma: endocrine abnormalities at presentation. Review uri icon

Overview

abstract

  • Craniopharyngioma is the most common childhood tumor to involve the hypothalamus and pituitary. Although endocrine disturbances can be found in 80-90% of patients at presentation, only a minority of subjects seek medical attention for an endocrine-related complaint. Hormonal studies, while limited, indicate GH deficiency in 75% of children; deficiencies of LH/FSH (40%), ACTH (25%) and TSH (25%) also are common. In contrast, diabetes insipidus has been noted in only 9-17% of subjects prior to surgery. When possible, full evaluation of pituitary function should be performed; the minimum preoperative evaluation must include testing for and treatment of ACTH-adrenal insufficiency and diabetes insipidus.

publication date

  • January 1, 1994

Research

keywords

  • Craniopharyngioma
  • Paraneoplastic Endocrine Syndromes
  • Pituitary Neoplasms

Identity

Scopus Document Identifier

  • 0028151172

PubMed ID

  • 7841073

Additional Document Info

volume

  • 21 Suppl 1