Purpose/introduction Craniopharyngiomas are locally-aggressive tumors arising along the
hypothalamic-pituitary axis. Treatment is nuanced as a result of their proximity and …

Background Craniopharyngioma treatment often necessitates surgical resection.
Conventional approaches, such as transcranial and transsphenoidal approaches, are …

OBJECTIVE Craniopharyngioma is a benign but surgically challenging brain tumor.
Controversies exist regarding its ideal treatment strategy, goals of surgery, efficacy of …

Papillary craniopharyngioma (PCP) is a rare type of tumor, comprising∼ 20% of all
craniopharyngioma (CP) cases. It is now recognized as a separate pathological entity from …

Purpose Craniopharyngiomas are histologically benign tumors, but their proximity to vital
neurovascular structures can significantly deteriorate functional prognoses and severely …

Introduction Wide variations exist in the management of craniopharyngiomas, including
pituitary stalk preservation/sacrifice. This study examines the practice patterns over 16 years …

Purpose Hypothalamic obesity (HO) is a complication associated with craniopharyngioma
(CP). Attempts have been made to perioperatively predict the development of this …

Background Various clinical classifications of craniopharyngiomas (CRPs) have been
proposed to suggest optimal surgical planning. We aimed to evaluate the clinical outcomes …

Purpose Craniopharyngiomas are rare tumors originating in the sellar region, with limited
information on their somatic mutational landscape. In this study, we utilized a publicly …

Objectives The two histologic subtypes of craniopharyngiomas (CPs), papillary and
adamantinomatous, harbor mutually exclusive mutations of BRAF V600E and CTNNB1 …