(Albany, US) DelveInsight has launched a new report on “Vestibular Schwannoma – Market Insights, Epidemiology, and Market Forecast-2030“.
DelveInsight’s “Vestibular Schwannoma – Market Insights, Epidemiology, and Market Forecast-2030“ report delivers an in-depth understanding of the Vestibular Schwannoma, historical and forecasted epidemiology as well as the Vestibular Schwannoma market trends in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan.
Some of the facts:
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Scope of the Report
Vestibular Schwannoma (also known as acoustic neuroma, acoustic neurinoma, or acoustic neurilemoma) is a benign, usually slow-growing tumor developed from the balance and hearing nerves supplying the inner ear. The tumor comes from an overproduction of Schwann cells that generally wrap around nerve fibers like onion skin to help support and insulate nerves.
It is classified as sporadic unilateral or hereditary bilateral. Sporadic Unilateral acoustic neuromas affect only one ear. It is the most common type of VS. This tumor may develop at any age. It most often happens between the ages of 30 and 60. Hereditary Bilateral acoustic neuromas: this type affects both ears and is inherited, and it is caused by a genetic problem called neurofibromatosis-2 (NF2).
The most common first symptom is hearing loss in the affected ear, which often goes unrecognized or is mistaken for a normal change of aging. Small tumors, which are typically limited to the bony canal, cause hearing loss in one ear, tinnitus (ringing in the ears), and unsteadiness or dizziness. As the tumor expands, hearing loss may worsen, facial weakness may occur, and balance problems (disequilibrium) may occur. Large tumors can compress the brainstem (causing imbalance) and the trigeminal nerve (causing facial numbness). As brainstem compression becomes severe, the fourth ventricle collapses, and hydrocephalus results, causing persistent headache and visual problems.
Neck or face radiation can lead to VS many years later. People who have a disease called neurofibromatosis type 2 (NF2) are also at higher risk. NF2 can run in families.
Some of the Vestibular Schwannoma Companies Covered:
Some of the Vestibular Schwannoma Drugs Covered:
Magnetic resonance imaging (MRI) is the method of choice for identifying suspected VS, with contrast-enhanced T1-weighted scans considered to be the gold standard for the initial evaluation and postoperative assessment of recurrence or residual tumors. The MRI protocol should include standard T1-and T2-weighted sequences, diffusion-weighted imaging (DWI), and fluid-attenuated inversion recovery sequences (FLAIR). DWI imaging is useful to differentiate VS from arachnoid or epidermoid cyst. Additionally, Computed Tomography (CT) has a complementary role in the evaluation of VS. It provides useful pre-operative information about the surgical anatomy of the skull base, especially the petrous bone.
Table of Contents:
5.1. Introduction
5.2. Sign and Symptoms
5.3. Pathophysiology
5.4. Risk Factors
5.5. Diagnosis
List to be continued in report
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About DelveInsight
DelveInsight is a leading Life Science market research and business consulting company recognised for its off-the-shelf syndicated market research reports as well as customised solutions to firms in the healthcare sector.
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