Management of craniopharyngiomas

被引:41
作者
Karavitaki, N. [1 ]
机构
[1] Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Dept Endocrinol, Oxford OX3 7LJ, England
关键词
Craniopharyngiomas; Pituitary; Hypothalamus; Hypopituitarism; GROWTH-HORMONE GH; HYPOTHALAMIC OBESITY; CYSTIC CRANIOPHARYNGIOMAS; INTRACAVITARY IRRADIATION; ONSET CRANIOPHARYNGIOMA; ENDOCRINE SEQUELAE; RADIATION-THERAPY; BARIATRIC SURGERY; CHILDREN; ADULTS;
D O I
10.1007/s40618-013-0050-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Craniopharyngiomas are rare epithelial tumours arising along the path of the craniopharyngeal duct. Their pathogenesis remains uncertain and they can present with a variety of manifestations attributed to pressure effects to surrounding structures. The optimal management of craniopharyngiomas remains challenging mainly due to their sharp, irregular borders and their tendency to adhere to vital neurovascular structures making surgical manipulations potentially hazardous to vital brain areas. Non-aggressive surgery followed by radiotherapy is currently the most widely used option possibly achieving the most optimal long-term outcome. Other treatment modalities including intracystic irradiation, intracystic instillation of antineoplasmatic agents and stereotactic radiotherapy are also available in our armamentarium. The long-term morbidities related with the craniopharyngiomas and their treatment remain significant, with hypothalamic damage playing the protagonist role and requiring further studies to identify measures that will improve the prognosis of the patients.
引用
收藏
页码:219 / 228
页数:10
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