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Internal auditory canal duplication with facial and cochlear nerve dysfunction: A case report
Roshan Ghising1, Kripa Dongol1, Sundar Suwal2
1Department of Otorhinolaryngology, Institute of Medicine, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
SAGE Open Medical Case Reports
|December 27, 2023
Summary
Internal auditory canal duplication is a rare temporal bone anomaly. This case highlights its association with facial nerve palsy and sensorineural hearing loss, diagnosed via advanced imaging.
Area of Science:
- Otolaryngology
- Radiology
- Anatomy
Background:
- Internal auditory canal (IAC) duplication is a rare congenital anomaly of the temporal bone.
- It involves a bony septum dividing the IAC into two compartments, potentially affecting cranial nerves.
Observation:
- A 26-year-old female presented with long-standing right-sided facial nerve palsy and sensorineural hearing loss.
- High-Resolution Computed Tomography revealed an incomplete bony septum in the right IAC.
- Magnetic Resonance Imaging confirmed normal caliber vestibulocochlear and facial nerves.
Findings:
- The patient exhibited moderate sensorineural hearing loss and Grade IV lower motor neuron facial nerve palsy.
- Imaging confirmed incomplete IAC duplication on the right side.
- The left IAC and other inner/middle ear structures were normal.
Implications:
- This case underscores the importance of advanced imaging in diagnosing rare IAC anomalies.
- Understanding IAC duplication is crucial for managing associated neurological deficits like facial palsy and hearing loss.
- Further research into the embryological basis and clinical spectrum of IAC duplication is warranted.
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