The Significance of a Hypoplastic Bony Canal for the Cochlear Nerve in Patients with Sensorineural Hearing Loss: CT and MRI Findings.
10.3348/jkrs.2004.50.4.227
- Author:
Yoon Jung CHOI
1
;
Sang Yoo PARK
;
Myung Soon KIM
;
Ki Jun SUNG
Author Information
1. Department of Radiology, Yonsei University Wonju College of Medicine, Wonju, Korea. s1k1j1@wonju.yonsei.ac.kr
- Publication Type:Original Article
- Keywords:
Temporal bone;
Temporal bone, abnormalities;
Temporal bone, MR;
Temporal bone, CT
- MeSH:
Cochlear Nerve*;
Constriction, Pathologic;
Hearing Loss, Sensorineural*;
Humans;
Magnetic Resonance Imaging*;
Retrospective Studies;
Temporal Bone;
Vestibulocochlear Nerve
- From:Journal of the Korean Radiological Society
2004;50(4):227-236
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: The purpose of this study is to evaluate the significance of the hypoplastic canal for the cochlear nerve in patients with sensorineural hearing loss (SNHL) and the relationship between the hypoplastic bony canal and aplasia or hypoplasia of the cochlear nerve. MATERIALS AND METHODS: A retrospective review of high resolution temporal CT(HRCT) and MRI findings was conducted. The narrow bony canal of the cochlear nerve and the relative size of the internal auditory canal were correlated with the cochlear nerve deficiency on MRI. The comparative size of the component nerves (facial, cochlear, superior vestibular, inferior vestibular nerve), and the relative size of the internal auditory canal and the bony canal of the cochlear nerve were measured. The clinical history and the results of the clinical examination were reviewed for each patient. RESULTS: High resolution MRI showed aplasia of the common vestibulocochlear nerve in one patient and a deficiency of the cochlear nerve in 9 patients. These abnormalities occurred in association with a prominent narrowing of the canal for the cochlear nerve and a stenosis of the internal auditory canal, which was observed on temporal bone CT in 9 patients with congenital SNHL. Three patients had normal IAC, despite the presence of a hypoplastic cochlear nerve on the side on which they had SNHL. In one patient, the narrowing of the canal for the cochlear nerve and internal auditory canal were not found to be associated with acquired SNHL. CONCLUSION: The hypoplastic bony canal for the cochlear nerve might be more highly indicative of congenital cochlear nerve deficiency than that of the narrow internal auditory canal, and the position of the crista falciformis should also be carefully.
