Results 81 to 90 of about 10,682 (216)

Immediate postoperative cardiac arrest after resection of a Giant Craniopharyngioma in a pediatric patient: A case report

JCA Advances
Craniopharyngioma resection in children is surgically challenging due to its proximity to critical hypothalamic and vascular structures, and although rare, sudden postoperative hemodynamic collapse may occur.
L. Pfokreni, MD, Ashutosh Kaushal, MD, DNB, PDCC, DM, Vaishali Waindeskar, MD, Basil Babu, MS, B. Niranjani, MD, Surya Kant, MD   +5 more
doaj   +1 more source

Molecular and cellular pathogenesis of adamantinomatous craniopharyngioma

, 2015
Adamantinomatous craniopharyngiomas (ACPs) are the most common pituitary tumours in children. Although histologically benign, these are clinically aggressive tumours, difficult to manage and associated with poor quality of life for the patients.
Martinez-Barbera, JP
core  

Global pediatric craniopharyngioma management modalities and outcomes

, 2023
Introduction: Pediatric craniopharyngioma is a complex pathology, with optimal management involving a multidisciplinary approach and thoughtful care coordination.
Khalid, Muhammad Usman, Mushtaq, Naureen, Haizel-Cobbina, Joseline, Peter-Okaka, Uchenna I, Tang, Alan R, Dewan, Michael C, Prosak, Olivia L   +6 more
core   +1 more source

A Nationwide Central Diagnosis for Pediatric CNS Tumors in Japan: The JCCG Brain Tumor and Pathology Committees

Cancer Science, Volume 117, Issue 7, Page 1975-1984, July 2026.
In this report, we present the results of a nationwide initiative launched by the Japan Children's Cancer Group to provide integrated diagnoses for pediatric central nervous system (CNS) tumors, incorporating central pathological review and molecular profiling.
Yoshiko Nakano, Junko Hirato, Takako Yoshioka, Tetsuya Takimoto, Sumihito Nobusawa, Kaishi Satomi, Ran Tomomasa, Seiji Yamada, Taku Homma, Shoh Sasaki, Ayako Yamazaki, Maki Sakaguchi, Yasuhide Takeuchi, Nei Fukazawa, Kai Yamasaki, Kohei Fukuoka, Yui Shinohara Kimura, Yuki Nagayama, Yohei Inoue, Akira Miyahira, Ema Yoshioka, Asako Katsuma, Hayato Fukusumi, Tomoko Shofuda, Yuko Hibiya, Yuko Matsushita, Mai Honda Kitahara, Yuki Yomoda, Miho Kato, Michael D. Taylor, Yasuhito Arai, Tatsuhiro Shibata, Hiroaki Sakamoto, Keita Terashima, Yoshiki Arakawa, Toshihiro Kumabe, Ryo Nishikawa, Junichi Hara, Yonehiro Kanemura, Koichi Ichimura   +39 more
wiley   +1 more source

Craniopharyngioma - Transnasal Endoscopic Approach

, 2011
Craniopharyngiomas are slow growing tumours arising from remnants of the craniopharyngeal duct and occupy the sellar region. The patients may remain asymptomatic for long duration or present with headache or visual disturbances.
Gupta, Nitin, SS Bist,, Saurabh Varshney,, Nitin Gupta,, Bhagat, Sanjeev, Varshney, Saurabh, Bist, SS, Sanjeev Bhagat,   +7 more
core  

Craniopharyngioma – case report and literature review

Journal of Education, Health and Sport
Craniopharyngiomas (Erdheim tumors) are rare tumors with low histological malignancy. Craniopharyngiomas occur at a rate of 0.5 to 2 cases per million people per year, accounting for 30 to 50% of all cases occurring in childhood and adolescence ...
Michał Leśniewski
doaj   +1 more source

Noninvasive molecular diagnosis of craniopharyngioma with MRI-based radiomics approach

BMC 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, Yusheng Tong, Zhifeng Shi, Hong Chen, Zhong Yang, Yuanyuan Wang, Liang Chen, Jinhua Yu   +7 more
doaj   +1 more source

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

PLoS 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, Nienke Veldhuis, Inge Stegeman, Hanneke M van Santen, Giorgio L Porro, Saskia M Imhof, Antoinette Y N Schouten-van Meeteren   +6 more
doaj   +1 more source

Neuromyelitis Optica Spectrum Disorder Following Pituitary Tumor Resection: A Rare but Critical Differential in Neurosurgical Practice

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Neuromyelitis optica spectrum disorder (NMOSD) is a rare, immune‐mediated astrocytopathy disorder that predominantly affects adults. Postoperative cases are scarcely reported. A 75‐year‐old woman underwent uncomplicated endoscopic resection of a nonfunctional pituitary macro‐adenoma.
Arad Iranmehr, Mohammad Shirani, Abdorreza Naser Moghadasi, Shirin Irani, Narges Akhlaghi, Samira Mirzaei, Hesam Ghadirian   +6 more
wiley   +1 more source

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

Journal 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, Dorota Ratuszek-Sadowska, Maciej Śniegocki   +2 more
doaj   +3 more sources