Imaging of Congenital and Acquired Sensorineural Hearing loss: Peeking through the Oval Window into the Cochlea and Beyond
Pure sensorineural hearing loss may be congenital or acquired. It can result from a constellation of abnormalities that may involve the labyrinth, internal auditory canal, CPA, brain stem, or auditory pathways. CT and MR imaging often play a complementary role in its evaluation and
postoperative assessment and in ascertaining overall prognosis. Herein we review the spectrum of pathology along the auditory pathway, extending from the labyrinth to the auditory cortex, that may present with sensorineural hearing.
Learning Objective: To recognize the imaging spectrum of sensorineural hearing loss in the pediatric and adult population.
Learning Objective: To recognize the imaging spectrum of sensorineural hearing loss in the pediatric and adult population.
Keywords: CHARGE = Coloboma, Heart defect, Atresia choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies/deafness; CMV = Cytomegalovirus; CN = cranial nerve; CND = cochlear nerve deficiency; CPA = cerebellopontine angle; ELST = endolymphatic sac tumor; EVAS = enlarged vestibular aqueduct syndrome; GA = gestational age; GRE = gradient recalled echo; IAC = internal auditory canal; SCC = semicircular canal; SNHL = sensorineural hearing loss
Document Type: Research Article
Publication date: September 1, 2013
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