Craniopharyngiomas are rare, mainly sellar/parasellar, epithelial tumors diagnosed during
childhood or adult life. Histologically, two primary subtypes have been recognized …

Object Craniopharyngiomas have a propensity to recur after resection, potentially causing
death through their aggressive local behavior in their critical site of origin. Recent data …

Objective Craniopharyngiomas are rare tumors with bimodal incidence in the pediatric and
adult age groups. Treatment strategies range from aggressive resection to planned limited …

Craniopharyngiomas are locally aggressive tumors which typically are focused in the sellar
and suprasellar region near a number of critical neural and vascular structures mediating …

Object Craniopharyngiomas are benign tumors but their close anatomical relationship with
critical neurological, endocrine, and vascular structures makes gross-total resection (GTR) …

To date, approximately 200 cases of atypical teratoid/rhabdoid tumor (AT/RT) of the central
nervous system have been described in the literature. This CNS tumor tends to present at an …

Radiotherapy remains the mainstay of multidisciplinary management of patients with
incompletely resected and recurrent craniopharyngioma. Advances in imaging and …

Craniopharyngioma (CP) represent 1.2-4.6% of all intracranial tumors in children and carry
a significant morbidity due to their lesional intimacy with structures involved in neurological …

The sellar and parasellar region is an anatomically complex area where a number of
neoplastic, inflammatory, infectious, developmental and vascular diseases can develop …

Background and purpose Treatment of patients with atypical teratoid/rhabdoid (AT/RT) is
challenging, especially when very young (below the age of three years). Radiotherapy (RT) …