Artigo
Craniopharyngioma
Fecha
2011-08-01Registro en:
Otolaryngologic Clinics of North America. Philadelphia: W B Saunders Co-Elsevier Inc, v. 44, n. 4, p. 937-+, 2011.
0030-6665
10.1016/j.otc.2011.06.015
WOS:000294371500008
Autor
Stamm, Aldo C.
Vellutini, Eduardo
Balsalobre, Leonardo [UNIFESP]
Institución
Resumen
Craniopharyngiomas are rare epithelial tumors arising along the path of the craniopharyngeal duct; therefore, they occur in the sellar or suprasellar regions. These tumors commonly lead to neurologic, endocrinological, or visual symptoms. Radical surgery is the treatment of choice in craniopharyngiomas. the transnasal/transsphenoidal endoscopic approach offers the possibility of removing the tumor without retracting brain and optic pathways, with good results. the rate of cerebrospinal fluid fistula has improved due to the use of vascularized mucosa; flaps for cranial base reconstruction.