Consequences of Craniopharyngioma Surgery in Children
Author(s) -
Hermann L. Müller
Publication year - 2011
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2011-0174
Subject(s) - craniopharyngioma , medicine , quality of life (healthcare) , radiation therapy , pituitary neoplasm , resection , pituitary tumors , surgery , pediatrics , pituitary gland , nursing , hormone
Childhood craniopharyngioma, a rare embryogenic tumorous malformation of the sellar region, is characterized by survival rates ranging from 91 to 98%. However, quality of survival is frequently impaired due to proximity to optical, pituitary, and hypothalamic structures. Long-term sequelae substantially reduce the quality of life of approximately 50% of long-term survivors, notably extreme obesity owing to hypothalamic involvement and/or surgical- or radiation-induced lesions.
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