Results 61 to 70 of about 8,269 (177)

Noninvasive molecular diagnosis of craniopharyngioma with MRI-based radiomics approach

open access: yesBMC Neurology, 2019
Background Frequent somatic mutations of BRAF and CTNNB1 were identified in both histological subtypes of craniopharyngioma (adamantinomatous and papillary) which shed light on target therapy to cure this oncogenic disease.
Xi Chen   +7 more
doaj   +1 more source

Normalization of Endocrine Function After Endoscopic Fenestration of an Anterior Third Ventricular Cyst: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Anterior third ventricular cysts may present solely with endocrine abnormalities due to subtle hypothalamic compression. Endoscopic fenestration can reverse hormone disturbances when imaging correlates with clinical findings. Structural CNS pathology should be considered in unexplained pediatric pubertal changes, and surgical decompression may
Thea Kadri, Tim Kadri, Hassan Kadri
wiley   +1 more source

Early Initiation of Adjuvant Therapy Following Pediatric Endoscopic Endonasal Surgery for Tumors

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 12, Issue 2, Page 189-194, April 2026.
ABSTRACT Objective To evaluate complication rates of early adjuvant therapy initiation in pediatric patients with endoscopic endonasal resection for skull base tumors. Design Retrospective case series of pediatric patients (0–18 years old) with skull base tumors who underwent endoscopic endonasal resection between 2013 and 2023.
Heta Patel   +7 more
wiley   +1 more source

Czaszkogardlak – rzadki łagodny guz nowotworowy - opis przypadku = Craniopharyngioma – rare benign tumor – case report

open access: yesJournal of Education, Health and Sport, 2016
Woźniak Kamila, Ratuszek-Sadowska Dorota, Śniegocki Maciej. Czaszkogardlak – rzadki łagodny guz nowotworowy - opis przypadku = Craniopharyngioma – rare benign tumor – case report. Journal of Education, Health and Sport. 2016;6(8):581-586.
Kamila Woźniak   +2 more
doaj   +3 more sources

Visual functions in children with craniopharyngioma at diagnosis: A systematic review.

open access: yesPLoS ONE, 2020
Childhood craniopharyngioma is a rare and slow growing brain tumour, often located in the sellar and suprasellar region. It commonly manifests with visual impairment, increased intracranial pressure and hypothalamic and/or pituitary deficiencies.
Myrthe A Nuijts   +6 more
doaj   +1 more source

Recent Advances in Diet and Exercise Interventions towards Craniopharyngioma-related Hypothalamic Obesity [PDF]

open access: yesZhongguo quanke yixue
Craniopharyngioma-related hypothalamic obesity (CHO) has become a key issue in postoperative management of craniopharyngioma. Modified low calorie diet and exercise interventions have been found by some studies to be effective in relieving CHO, and ...
REN Ying, WANG Chaohu, ZHANG Nannan, BAO Yun, QI Songtao, DENG Yingying
doaj   +1 more source

Evaluation and Management of Symptomatic Vasospasm following Endoscopic Endonasal Resection of Pediatric Adamantinomatous Craniopharyngioma

open access: yesCase Reports in Pediatrics, 2020
Background. Cerebral vasospasm is a well-described pathology following subarachnoid hemorrhage and trauma in children; however, very few cases have been published following craniopharyngioma resection in children.
Dustin Hansen   +4 more
doaj   +1 more source

Long-term outcomes of pediatric craniopharyngioma patients after surgical resection

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery
Objective To review the effect of resection of pediaric craniopharyngioma and the long-term quality of life. Methods The clinical datas before, during and after operation of 30 pediatric craniopharyngioma patients who were operated in Xuanwu Hospital ...
ZHOU Ma-ding   +4 more
doaj   +1 more source

A Rare Case of Craniopharyngioma in the Temporal Lobe

open access: yesCase Reports in Neurological Medicine, 2017
Herein, we report on a rare case of craniopharyngioma arising in the left temporal lobe with no prior history of head trauma or surgery. There was a solid-cystic mass in the left temporal lobe on MR images.
Sasan Razmjoo   +3 more
doaj   +1 more source

A rare challenging case of co-existent craniopharyngioma, acromegaly and squamous cell lung cancer

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2018
Co-existence of craniopharyngioma and acromegaly has been very rarely reported. A 65-year-old man presented with visual deterioration, fatigue and frontal headaches. Magnetic resonance imaging revealed a suprasellar heterogeneous, mainly cystic, 1.9 × 2 ×
Athanasios Fountas   +5 more
doaj   +1 more source

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