CT Imaging Categorization and Biomarker Study of Anomalous Tympanic Segment of the Facial Nerves in Patients With Hearing Loss in the Absence of Microtia
| Autor: | Nisa Cem Oren, Daniel Thomas Ginat |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Male
Adolescent Hearing loss Hearing Loss Sensorineural Hearing Loss Conductive CHARGE syndrome Temporal bone otorhinolaryngologic diseases Medicine Humans Inner ear Oval Window Ear Child Stapes Retrospective Studies business.industry Microtia Oval window Infant Temporal Bone Anatomy Middle Aged medicine.disease Conductive hearing loss Facial Nerve medicine.anatomical_structure Otorhinolaryngology Child Preschool Ear Inner Female medicine.symptom business Tomography X-Ray Computed |
| Zdroj: | Ear, nose,throat journal. 98(6) |
| ISSN: | 1942-7522 |
| Popis: | The purpose of this study is to categorize anomalous tympanic facial nerve (FN) on high-resolution computed tomography (HRCT) and to determinate the significance of associated temporal bone anomalies and congenital syndromes without microtia in patients with hearing loss. A retrospective analysis of HRCT findings in 30 temporal bones in 18 patients with anomalous FN was performed. Abnormalities of the tympanic FN were categorized as follows: category 1: FN medially positioned, but above the oval window; category 2: FN in the oval window niche; and category 3: FN below the oval window. Potential associated findings that were assessed included stapes abnormalities, oval window atresia, and inner ear anomalies, as well as the presence of a known congenital syndrome with hearing loss. The most common type of anomalous tympanic FN was category 1 (67%, n = 20), following by group 2 (20%, n = 6) and group 3 (13%, n = 4). Stapes anomalies were detected in 77% of temporal bones (n = 23), oval window atresia was detected in 43% of temporal bones (n = 13), and inner ear anomalies were detected in 70% of temporal bones (n = 21). Anomalous tympanic facial nerves in temporal bone with conductive hearing loss were often (60%) not associated with oval window atresia. The combination of aberrant tympanic FN and inner ear anomalies was significantly ( P = .038) associated with a known congenital syndrome (6 patients), including CHARGE syndrome, oculo-auriculo-vertebral spectrum, Pierre-Robin sequences, and Down syndrome. Therefore, an anomalous tympanic FN in conjunction with inner ear anomalies appears to be a biomarker for certain congenital syndromes with hearing loss in the absence of microtia. |
| Databáze: | OpenAIRE |
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