Results 11 to 20 of about 8,724 (184)

Craniopharyngioma [PDF]

open access: yesNature 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

Craniopharyngioma [PDF]

open access: yesJournal 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

Craniopharyngiomas [PDF]

open access: yesJournal of Neuroscience Nursing, 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

Third Ventricular Chordoid Glioma With TTF-1 Positivity: A Diagnostic and Therapeutic Challenge. [PDF]

open access: yesClin Case Rep
ABSTRACT Third ventricular chordoid glioma is a rare tumor often misdiagnosed due to nonspecific imaging. TTF‐1 immunoreactivity is critical for definitive diagnosis. Management should be individualized, balancing gross resection, adjuvant radiotherapy, and surveillance depending on surgical risk and recurrence potential.
Shen Z, Zhang B, Zhu X.
europepmc   +2 more sources

Lower social participation and physical activity in patients with craniopharyngioma or CNS germ cell tumor: Their association with apathy. [PDF]

open access: yesPCN Rep
Abstract Aim This study aimed to compare social participation and physical activity in patients with craniopharyngioma or central nervous system germ cell tumor (CNS germ cell tumor) with those of healthy participants and examine their associations with social behavioral disorders.
Komaki M   +10 more
europepmc   +2 more sources

Proton beam therapy in paediatric cancer: Anticipating the opening of the Australian Bragg Centre for Proton Therapy and Research

open access: yesJournal of Medical Imaging and Radiation Oncology, EarlyView., 2023
Summary Proton Beam Therapy (PBT) has the potential to improve paediatric cancer care by reducing radiation exposure and thus long‐term toxicities. Ethical concerns and debates surrounding the treatment, such as eligibility and accessibility, are ongoing in Australia. The Australian Bragg Centre for Proton Therapy and Research (ABCPTR) (named after Sir
Jeremy Khong   +10 more
wiley   +1 more source

Application of Artificial Intelligence in Diagnosis of Craniopharyngioma

open access: yesFrontiers 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

open access: yesFrontiers 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

Craniopharyngiomas [PDF]

open access: yesNeurosurgery Clinics of North America, 1985
ABSTRACT:A review has been carried out of those patients with a craniopharyngioma who were treated initially in our institution and had a microsurgical excision of their tumour during the period of time when newer and sophisticated modalities of investigation and treatment were available.
openaire   +3 more sources

Craniopharyngioma with malignant transformation: A case report

open access: yesOral 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

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