• R. Du
  • R. H. Lustig
  • B. Fisch
  • M. W. McDermott
Part of the Pediatric Oncology book series (PEDIATRICO)


Craniopharyngiomas are histologically benign neuroepithelial tumors that arise from squamous cell rests found along the path of the primitive craniopharyngeal duct and adenohypophysis. They frequently involve vital structures in the sellar region including the optic apparatus and the pituitary, and often lead to visual, endocrine, and mental disturbances. Thus, despite their benign histology, the involvement of various neural structures in the suprasellar region makes the treatment and management of craniopharyngiomas difficult. There is an ongoing controversy regarding optimal treatment of craniopharyngiomas. The debate revolves around the risks and benefits of attempted gross total resection as compared to subtotal resection or biopsy followed by adjunctive therapy such as external beam radiotherapy, radiosurgery, intracavitary radiation, and/or chemotherapy.


Stereotactic Radiosurgery Subtotal Resection Transsphenoidal Approach Hypothalamic Obesity Intracavitary Irradiation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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Copyright information

© Springer-Verlag Berlin Heidelberg 2004

Authors and Affiliations

  • R. Du
  • R. H. Lustig
  • B. Fisch
  • M. W. McDermott

There are no affiliations available

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