Results 41 to 50 of about 114,822 (268)

Radiosurgery for vestibular schwannomas

open access: yesIndian Journal of Neurosurgery, 2014
Vestibular schwannomas (VS) are benign tumours arising from the 8th cranial nerve. There are various treatment options for these tumours, which depend upon the tumour size and patient age.
Sumit Sinha, A.K. Mahapatra
doaj   +1 more source

Subtotal resection of vestibular schwannoma: evaluation with Ki-67 measurement, magnetic resonance imaging, and long-term observation [PDF]

open access: yes, 2017
Purpose The aim of this study was to compare the postoperative clinical and radiological data of patients with vestibular schwannomas who were initially managed by near total resection (NTR) or subtotal resection (STR).
Angeletti, Diletta   +8 more
core   +1 more source

Stereotactic Radiosurgery for Vestibular Schwannomas: Reducing Toxicity With 11 Gy as the Marginal Prescribed Dose

open access: yesFrontiers in Oncology, 2020
BackgroundStereotactic radiosurgery (SRS) is a common treatment option for vestibular schwannomas. Historically, a dose de-escalation of the marginal prescribed dose from 16 Gy to 12–13 Gy has been done to limit toxicity without reducing local control ...
Guillaume Dupic   +12 more
doaj   +1 more source

Cochlear Implantation in Intralabyrinthine Schwannoma: Case Series and Systematic Review of the Literature

open access: yesAudiology Research, 2023
Intralabyrinthine schwannomas (ILS) are rare benign tumours arising from the peripheral branches of the cochlear or vestibular nerves in the membranous labyrinth, intracochlear schwannomas being the most frequent ones.
Sebastiano Franchella   +4 more
doaj   +1 more source

A proteasome-resistant fragment of NIK mediates oncogenic NF-κB signaling in schwannomas [PDF]

open access: yes, 2019
Schwannomas are common, highly morbid and medically untreatable tumors that can arise in patients with germ line as well as somatic mutations in neurofibromatosis type 2 (NF2).
Angus, Steven P.   +23 more
core   +1 more source

SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis

open access: yesBMC Neurology, 2011
Background Schwannomatosis is a disease characterized by multiple non-vestibular schwannomas. Although biallelic NF2 mutations are found in schwannomas, no germ line event is detected in schwannomatosis patients.
Bourdon Violaine   +4 more
doaj   +1 more source

The Management and Imaging of Vestibular Schwannomas

open access: yesAmerican Journal of Neuroradiology, 2017
SUMMARY: Vestibular schwannomas are the most common cerebellopontine angle tumor. During the past century, the management goals of vestibular schwannomas have shifted from total resection to functional preservation.
E. Lin, B. Crane
semanticscholar   +1 more source

Hypoglossal schwannoma masquerading as a carotid body tumor. [PDF]

open access: yes, 2012
Study Objective. To describe the clinical presentation, evaluation, and treatment of a hypoglossal schwannoma. Methods. We report an unusual case of a hypoglossal schwannoma presenting as a pulsatile level II neck mass at the bifurcation of the external ...
Abie H. Mendelsohn   +4 more
core   +1 more source

Endoscopic third ventriculostomy in hydrocephalus secondary to vestibular schwannomas

open access: yesRevista Cubana de Medicina Militar, 2023
Introduction: Treatment options for hydrocephalus related to posterior fossa tumors have been extensively studied in the pediatric population, but the value of endoscopic third ventriculostomy in hydrocephalus secondary to vestibular schwannoma in adults,
Ernesto Enrique Horta-Tamayo   +5 more
doaj  

Cranial Manifestations of Neurofibromatosis Type 2: A Rare Case Demonstrating 15 Intracranial Lesions

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth, 2020
Neurofibromatosis type 2 (NF-2) is a rare autosomal dominant disorder characterized by multiple neoplasms which include meningiomas, schwannomas, and ependymomas. The most common tumors associated with NF-2 are bilateral vestibular schwannomas. We report
Amit Kharat   +3 more
doaj   +1 more source

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