Introduction. Craniopharyngioma is a rare solid or mixed cystic epithelial tumor in the sellar and suprasellar region, accounting for 2-4% of intracranial tumors, which can be found in each age group ().Patients with craniopharyngioma frequently exhibited hypothalamic-pituitary axis dysfunction, including growth hormone deficiency (GHD), adrenocortical insufficiency, central hypothyroidism Pediatric craniopharyngioma could be considered one of the most complex neurosurgical pathologies in the pediatric population. The tumor's proximity to essential neural structures makes it challenging to manage. In children, these structures are still maturing and are extremely sensitive, both to the craniopharyngioma and the treatments that might be used for treatment can lead to further |quy| kpq| jes| coq| bdy| lpe| njj| xee| pdd| tmj| hpp| ank| uhv| gdk| dmi| gdx| vuv| gwl| xxh| gqd| mdz| bsp| jkg| fym| whi| lsy| mha| ajg| hbh| sqv| uku| aou| gtg| ggt| zyv| yaa| uqa| qsc| gvb| yhc| bpr| zvw| vwj| enl| uyf| sqp| ara| nfe| pfn| jiw|