
pmid: 17089867
In summary, much progress has been made in our understanding of childhood craniopharyngiomas. These histologically benign but "geographically malignant" tumors are challenging to treat and require experienced clinicians from multiple disciplines including neurosurgery, radiology, hematology/oncology, ophthalmology, endocrinology, and general pediatrics to address the multiple issues that arise with diagnosis, treatment, and long-term follow-up of affected children. The study and close observation of patients who have craniopharyngiomas may also be beneficial for our general understanding of pathophysiologic processes such as the observed "growth without growth hormone" phenomenon or the well-described and studied hypothalamic obesity phenotypes.
Wnt Proteins, Craniopharyngioma, Hypothalamo-Hypophyseal System, Growth Hormone, Humans, Pituitary Neoplasms, Radiotherapy Dosage, Obesity, Child, Combined Modality Therapy
Wnt Proteins, Craniopharyngioma, Hypothalamo-Hypophyseal System, Growth Hormone, Humans, Pituitary Neoplasms, Radiotherapy Dosage, Obesity, Child, Combined Modality Therapy
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