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Published on: March 2, 2018
Children with posterior semicircular canal dehiscence: A case series
Pauline Van Bulck1, Pieter-Jan Leupe1, Glen E J Forton1
1Department of Otolaryngology, AZ Delta, Wilgenstraat 2, 8800, Roeselare, Belgium.
Insights
Posterior semicircular canal dehiscence (PSCD) is a rare condition in children presenting with diverse symptoms like Tullio phenomenon or hearing loss. A conservative approach is often recommended due to surgical risks and potential symptom resolution with skull base maturation.
Area of Science:
- Otolaryngology
- Neuroscience
- Pediatric Medicine
Background:
- Posterior semicircular canal dehiscence (PSCD) is an uncommon condition.
- It can manifest with varied auditory and vestibular symptoms.
Observation:
- Three pediatric cases (ages 5-12) of right-sided PSCD are presented.
- Etiology identified as a prominent jugular bulb (high-riding bulb).
- Clinical presentations included Tullio phenomenon, conductive hearing loss, and pulsatile tinnitus.
Findings:
- Audiometric and radiological evaluations confirmed PSCD.
- The high-riding jugular bulb was a consistent finding in all cases.
- Diverse symptoms highlight the varied clinical impact of PSCD.
Implications:
- A conservative 'wait and see' management strategy is suggested for children.
- This approach minimizes surgical risks and considers natural symptom improvement.
- Skull base osseous maturation may lead to symptom resolution, supporting conservative care.
Abstract:
Posterior semicircular canal dehiscence is a rare condition and can cause a variety of symptoms. We report three cases of children between 5 and 12 years of age with a PSCD. They all presented with different complaints as follows: Tullio phenomenon in the first case, conductive hearing loss in the second and, conductive hearing loss and pulsatile tinnitus in the third. Imaging showed in all cases a PSCD on the right side, caused by a prominent jugular bulb (high riding bulb). We describe the clinical, audiometric and radiological findings, and discuss the management and therapy. A conservative "wait and see" approach is recommended, especially with children, because of the possible complications of surgery and the possibility that the symptoms will lessen with the skull base osseous maturation.
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