Results 11 to 20 of about 8,269 (177)
Endocrine Reviews, 2006 Craniopharyngiomas are rare benign epithelial tumors, arising from the pituitary stalk or gland and developing in the sellar and suprasellar region, affecting both adults and children. Incidence is 0.5 to 2 new cases per million inhabitants. Clinical features essentially include visual disturbances, endocrine deficiencies, and neurological signs ...
R, Van Effenterre, A-L, Boch
+7 more sources
Nature Reviews Disease Primers, 2019 Craniopharyngiomas are rare malformational tumours of low histological malignancy arising along the craniopharyngeal duct. The two histological subtypes, adamantinomatous craniopharyngioma (ACP) and papillary craniopharyngioma (PCP), differ in genesis and age distribution. ACPs are diagnosed with a bimodal peak of incidence (5-15 years and 45-60 years),
Müller, HL +4 more
openaire +5 more sources
Journal of Neurosurgery: Pediatrics, 2007 AbstractCraniopharyngiomas are benign slow growing tumours that are located within the sellar and para sellar region of the central nervous system. The point prevalence of this tumour is approximately 2/100,000. The onset of symptoms is normally insidious with most patients at diagnosis having neurological (headaches, visual disturbances) and endocrine
Grill Jacques +3 more
openaire +5 more sources
Nonalcoholic fatty liver disease in long-term survivors of childhood-onset craniopharyngioma [PDF]
Annals of Pediatric Endocrinology & Metabolism, 2017 Purpose Hypothalamic obesity in childhood-onset (CO-) craniopharyngioma patients may predispose to nonalcoholic fatty liver disease (NAFLD). This study reviewed the characteristics of NAFLD associated with CO-craniopharyngioma.
So Yoon Jung +7 more
doaj +1 more source
The research of craniopharyngioma classification
Chinese Journal of Contemporary Neurology and Neurosurgery, 2023 The tumor tissue of craniopharyngioma is closely adherent to peripheral neurovascular tissue, so the operation to remove lesion is more difficult, the perioperative complications are very serious, and the prognosis of patients is poor.
SI Liang⁃nan +2 more
doaj +1 more source
Application of Artificial Intelligence in Diagnosis of Craniopharyngioma
Frontiers in Neurology, 2022 Craniopharyngioma is a congenital brain tumor with clinical characteristics of hypothalamic-pituitary dysfunction, increased intracranial pressure, and visual field disorder, among other injuries.
Caijie Qin +4 more
doaj +1 more source
Stereotactic Neurosurgical Treatment Options for Childhood Craniopharyngioma
Frontiers in Endocrinology, 2012 Craniopharyngioma are the most common non glial tumors in childhood. The results of different studies indicate that radical excision surgery is not an appropriate treatment strategy for childhood craniopharyngioma with hypothalamic involvement ...
Michael eTrippel, Guido eNikkhah
doaj +1 more source
Craniopharyngioma with malignant transformation: A case report
Oral and Maxillofacial Surgery Cases, 2020 Introduction: Craniopharyngiomas are usually slow growing, benign epithelial tumors, arising from cell remnants of Rathke's pouch with its ultimate site of origin being the embryologic stomadeum.
Janssens E +6 more
doaj +1 more source
Diabetes Insipidus Pascaoperasi pada Pasien dengan Reseksi Tumor Kraniofaringioma
Jurnal Neuroanestesi Indonesia, 2023 Craniopharyngioma is an embryonic malformation in the sella and parasella areas. Craniopharyngioma has high survival rate, although the patient's quality of life is often compromised due to tumor’s location near important anatomical structures such as ...
I Putu Pramana Suarjaya +2 more
doaj +1 more source
Journal of Neurosurgery, 2008 Craniopharyngiomas are epithelial tumors arising along the path of the craniopharyngeal duct and presenting with a variety of manifestations. Their optimal management remains a subject of debate. Currently, surgical excision followed by external beam irradiation is the main treatment option.
CAPPABIANCA, PAOLO +3 more
openaire +5 more sources