Results 51 to 60 of about 8,724 (184)

Childhood craniopharyngioma [PDF]

open access: yesPituitary, 2008
<i>Background:</i> Craniopharyngioma are embryogenic malformations of the sellar area. With an overall incidence of 0.5–2 new cases per million population per year, 30–50% of all cases occur in childhood. Overall survival rates are high.
openaire   +2 more sources

Cancer pain: current practice and emerging targets

open access: yesBritish Journal of Pharmacology, EarlyView.
Cancer pain (CP) arises from a complex interplay between the tumour and its microenvironment. Many patients experience a mixed pain phenotype that encompasses nociceptive, neuropathic and neuroinflammatory mechanisms, and vary across tumour type and disease stage. Despite decades of intensive research, the mainstay of cancer pain treatment is still non‐
Yi Ye   +5 more
wiley   +1 more source

Hypopituitarism as a result of recurrent craniopharyngioma

open access: yesМедицинский вестник Юга России, 2020
The article presents a clinical observation of a patient with a complication of endoscopic endonasal removal of craniopharyngioma in the form of hypopituitarism.
Z. R. Alimetova, A. I. Galieva
doaj   +1 more source

Diagnostic Yield of Brain MRI in Pediatric Short Stature: Hypothalamic–Pituitary Lesions and Incidental Findings in Real‐World Practice

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Background Brain MRI is widely performed in children with short stature or suspected growth hormone deficiency(GHD) to exclude hypothalamic–pituitary (HP) pathology, yet its diagnostic yield in routine practice is uncertain. We aimed to evaluate the prevalence, clinical significance, and distribution of HP and extrahypothalamic abnormalities ...
Mustafa Zubeidat   +2 more
wiley   +1 more source

Insights into body composition in pediatric craniopharyngioma patients after surgical treatment

open access: yesTherapeutic Advances in Endocrinology and Metabolism
Background: Craniopharyngioma, a benign suprasellar tumor, is typically treated surgically with radiotherapy when indicated. Due to its proximity to the pituitary-hypothalamic region, patients often experience endocrine deficiencies.
Hussein Zaitoon   +8 more
doaj   +1 more source

Body Composition Remodelling During GLP‐1‐Based Therapy: A Systematic Review and Meta‐Analysis Using a Hierarchical Physiological Framework

open access: yesDiabetes, Obesity and Metabolism, EarlyView.
ABSTRACT Background Body composition changes during glucagon‐like peptide‐1 (GLP‐1)‐based therapy remain incompletely characterized, particularly regarding their effects on adiposity, muscle quantity, and muscle quality. We conducted a systematic review and meta‐analysis using a predefined physiological framework to evaluate body composition ...
Maria Luizza Lopes Menezes   +6 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

The relationship between psychosocial risk and neurocognitive functioning early after childhood central nervous system tumour diagnosis

open access: yesJournal of Neuropsychology, EarlyView.
Abstract Neurocognitive impairments are common in paediatric central nervous system (CNS) tumours and can relate to clinical and demographic factors. The impact of social or environmental factors, such as family psychosocial risk, is less well understood.
Jessica Beamish   +5 more
wiley   +1 more source

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

open access: yesJCA 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   +5 more
doaj   +1 more source

HierAnom‐Path: Zero‐Shot Rare Cancer Detection in Histopathology via Hierarchical Foundation Model Adaptation

open access: yesComputational and Systems Oncology, Volume 6, Issue 1, December 2026.
ABSTRACT Rare cancers collectively represent 20%–25% of all malignancies yet yield fewer than 50 annotated whole‐slide images (WSIs) per subtype in publicly available archives, rendering supervised deep learning inapplicable. We present HierAnom‐Path, to the best of our knowledge, the first framework for zero‐shot rare cancer anomaly detection in ...
Noora Saleem Jumaah   +5 more
wiley   +1 more source

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