Results 51 to 60 of about 67,419 (282)

Labyrinthine artery aneurysm as an internal auditory canal mass. [PDF]

open access: yes, 2014
We present the first case report of a labyrinthine artery aneurysm masquerading as an internal auditory canal tumor. A 72-year-old woman presented with sudden onset right facial paralysis, facial pain, hearing loss, and vertigo.
Brunberg, James   +2 more
core   +1 more source

Biphenotypic Sinonasal Sarcoma-Case Report and Review of Clinicopathological Features and Diagnostic Modalities. [PDF]

open access: yes, 2019
Background Biphenotypic sinonasal sarcoma is a recently described malignancy showing dual differentiation with both myogenic and neural elements. Due to its histologic similarities to other sinonasal malignancies, it is a diagnostic challenge.
Chitguppi, Chandala   +6 more
core   +2 more sources

Radiologic Findings of Renal Schwannoma: A Case Report and Literature Review

open access: yes대한영상의학회지, 2018
Schwannoma is a benign nerve sheath tumor that involves Schwann cells mostly found in the head, neck, posterior mediastinum and extremities.
Sung Tae Hwang   +6 more
doaj   +1 more source

Surgical treatment of sporadic vestibular schwannoma in a series of 1006 patients. Trattamento chirurgico degli schwannomi vestibolari: risultati su una serie di 1006 pazienti [PDF]

open access: yes, 2016
La gestione dello schwannoma vestibolare (SV) sporadico si è gradualmente evoluta negli ultimi decenni. Lo scopo di questo studio è di analizzare l’evoluzione negli esiti chirurgici dell’exeresi di queste lesioni, realizzata da un team neurotologico tra
BERNARDESCHI, DANIELE   +7 more
core   +2 more sources

MAXILLARY SINUS SCHWANNOMA EXTENDING TO ORBIT

open access: yesJournal of Nepal Medical Association, 2003
Schwannoma occur in the head and neck region more frequently than in any other part of the body, affecting mainly the eighth cranial nerve. However schwannoma in the nasal cavity and paranasal sinuses is a rare entity with only sporadic cases appearing ...
Ravinder Sharma   +3 more
doaj   +1 more source

Patient Decision Making in Vestibular Schwannoma: A Survey of the Acoustic Neuroma Association. [PDF]

open access: yes, 2018
Objective To assess the decision-making process of patients with vestibular schwannoma (VS). Study Design Patients with VS completed a voluntary survey over a 3-month period.
Djalilian, Hamid R   +4 more
core   +1 more source

Image findings of cranial nerve pathology on [18F]-2- deoxy-D-glucose (FDG) positron emission tomography with computerized tomography (PET/CT): a pictorial essay. [PDF]

open access: yes, 2015
This article aims to increase awareness about the utility of (18)F -FDG-PET/CT in the evaluation of cranial nerve (CN) pathology. We discuss the clinical implication of detecting perineural tumor spread, emphasize the primary and secondary (18)F -FDG-PET/
Muzaffar, Razi   +3 more
core   +1 more source

Schwannoma lingual: presentación de un caso y breve revisión de la literatura// Lingual schwannoma: case report and brief review of the literature

open access: yesRevista de la Asociación Odontológica Argentina, 2021
Resumen Objetivo: Reportar un caso de schwannoma lingual, así como revisar las características diagnósticas (clínicas, por imágenes e histopatológicas) y terapéuticas de esta patología mediante las publicaciones disponibles.
Ignacio Venturino
doaj   +1 more source

Schwannoma of the tongue in a child [PDF]

open access: yes, 2010
A schwannoma or neurilemmoma is a benign, slow growing, usually solitary and encapsulated tumour originating from Schwann cells of the nerve sheath.
Lukšić, Ivica   +4 more
core   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim   +9 more
wiley   +1 more source

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