Results 111 to 120 of about 89,743 (308)

Pancreatic schwannoma: a case report and an updated 40-year review of the literature yielding 68 cases

open access: yesBMC Cancer, 2017
Pancreatic schwannoma is a rare tumor. Preoperative diagnosis of pancreatic schwannoma is challenging due to its tendency to mimic other lesions of the pancreas.
Yuntong Ma   +8 more
semanticscholar   +1 more source

Schwannoma of the nasal septum-a case report [PDF]

open access: yes, 2012
Schwannomas of the nasal cavity and paranasal sinuses are very rare. We report the case of a50-year-old woman with a schwannoma arising from the nasal septum.
Felix, Vinod   +2 more
core   +1 more source

Trigeminal schwannoma

open access: yesNational Journal of Maxillofacial Surgery, 2017
Schwannoma is a benign tumor of the nerve sheath arising from the perineural schwann cells. The nerves most commonly involved in schwannomas of the head and neck are the vagus and the cervical sympathetic chain. Trigeminal schwannomas are rare tumours. A 17 year old male patient with a chief complaint of swelling on face was diagnosed as suffering from
Agrawal, Aviral   +3 more
openaire   +3 more sources

Imaging diagnosis: magnetic resonance imaging of diffuse leptomeningeal oligodendrogliomatosis in a dog with "dural tail sign" [PDF]

open access: yes, 2018
A case of diffuse leptomeningeal oligodendrogliomatosis affecting the brain and spinal cord of a dog is presented. A 7.5-year old, male neutered Staffordshire bull terrier presented for evaluation of a chronic history of tetraparesis and seizures, with a
Anwer   +31 more
core   +1 more source

MRI Enhancement Patterns After Resection of Sporadic Vestibular Schwannoma: Comparing Retrosigmoid and Translabyrinthine Approaches

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.
ABSTRACT Objective One theoretical disadvantage of the retrosigmoid approach is the inability to visualize tumor at the fundus of the internal auditory canal, potentially leading to a higher risk of residual tumor even when the surgeon reports a gross total resection.
Olivia La Monte   +6 more
wiley   +1 more source

Global Proteome and Phospho-proteome Analysis of Merlin-deficient Meningioma and Schwannoma Identifies PDLIM2 as a Novel Therapeutic Target [PDF]

open access: yes, 2017
Loss or mutation of the tumour suppressor Merlin predisposes individuals to develop multiple nervous system tumours, including schwannomas and meningiomas, sporadically or as part of the autosomal dominant inherited condition Neurofibromatosis 2 (NF2 ...
Ammoun   +80 more
core   +4 more sources

Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development

open access: yesNature Communications, 2017
Germline mutations of the SMARCB1 gene predispose to two distinct tumor syndromes: rhabdoid tumor predisposition syndrome, with malignant pediatric tumors mostly developing in brain and kidney, and familial schwannomatosis, with adulthood benign tumors ...
Jeremie Vitte   +4 more
semanticscholar   +1 more source

Ongoing Discrepancy Between Unilateral Meniere's Disease and Bilateral Endolymphatic Hydrops on Hydrops MRI

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.
ABSTRACT Objective In the era of Hydrops MRI, a clinical dilemma has emerged: while Meniere's disease (MD) is diagnosed unilaterally, Hydrops MRI demonstrates endolymphatic hydrops (EH) bilaterally. This study aims to clarify this ongoing discrepancy. Methods Fifty‐six MD patients underwent an inner ear test battery followed by 3 T Hydrops MRI.
Ting‐Hua Yang   +2 more
wiley   +1 more source

Schwannoma—A Rare Subepithelial Lesion of the Colon

open access: yesGE: Portuguese Journal of Gastroenterology, 2015
Schwannoma is a benign tumor arising from Schwann cells that form the neural sheath. Primary schwannoma of the colon is rare and a few cases have been reported.
Sandra Barbeiro   +9 more
doaj   +1 more source

Malignant Rhabdoid Tumors of Cranial Nerves—A Clinically Distinct Group With Characteristic Neuroradiological, Histopathological, and Molecular Features

open access: yesPediatric Blood &Cancer, Volume 72, Issue 8, August 2025.
ABSTRACT Background Malignant rhabdoid tumors occasionally develop along cranial nerves, but clinical, histopathological, and molecular features have not been examined in larger series. Procedure We retrospectively interrogated data from the European Rhabdoid Registry, EU‐RHAB, to identify malignant rhabdoid tumors affecting cranial nerves.
Miriam Gruhle   +15 more
wiley   +1 more source

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