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Revista de otorrinolaringología y cirugía de cabeza y cuello

versión On-line ISSN 0718-4816

Resumen

STOTT C, Carlos; ALBERTZ A, Nicolás  y  AEDO B, Cristian. Acoustic neuroma (vestibular schwannoma): A literature rev. Rev. Otorrinolaringol. Cir. Cabeza Cuello [online]. 2008, vol.68, n.3, pp.301-308. ISSN 0718-4816.  http://dx.doi.org/10.4067/S0718-48162008000400012.

Acoustic neuroma is the most frequent ponto cerebellar angle tumor. Genetic factors are involved in its etiology and in occasions its origins can be linked to diseases such as bilaterally expressing type 2-neurofibromatosis. Clinically acoustic neuromas can be classified in 4 stages, which result in diverse symptoms, according to the degree ofbrain stem and interna I auditory canal compression or obstruction; however, hearing loss remains as the most important presenting symptom. The four stages are: intracanalicular, cisternal, brain stem compressive and hydrocephalic. Frequently they reach between few millimeters to more than 3 centimeters in diameter, and are accordingly ranked as small, medium-sized, and large. They have been reponed as having slow growth and uncertain natural history; in most studies growth rafes fluctuate between 1-3 mm/year Pure tone audiometry is the procedure of chote for diagnosis orientation in the first place, however, gadolinium-contrasted magnetic resonance imaging is currently pivotal for diagnosis confirmation. As for management, there are three reasonable alternatives, depending on a given case particularity. These are monitoring, microsurgery and stereotactic radiotherapy or gamma knife. Each one of them has its pros and cons, and thus the final therapy decisión will depend on the symptoms and tumor growth rate andsize, príorizlng thepatient well-being.

Palabras clave : Acoustic neuroma; vestibular neuroma; vestibular schwannoma; ponto cerebellar angle tumor.

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