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This study aimed to validate the role of 3D segmentation in measuring the volume of the vestibular aqueduct (VAD), and the inner ear, and to study the correlation between VAD volume and VAD linear measurements at the midpoint and operculum. The correlation with other cochlear metrics was also studied. We retrospectively recruited 21 children (42 ears) diagnosed with Mondini dysplasia (MD) plus enlarged vestibular aqueduct (EVA) from 2009 to 2021 and who underwent cochlear implantation (CI). Patients' sociodemographic data were collected, and linear cochlear metrics were measured using Otoplan. Vestibular aqueduct width and vestibular aqueduct and inner ear volumes were measured by two independent neuro-otologists using 3D segmentation software (version 4.11.20210226) and high-resolution CT. We also conducted a regression analysis to determine the association between these variables and CT VAD and inner ear volumes. Among the 33 cochlear implanted ears, 13 ears had a gusher (39.4%). Regarding CT inner ear volume, we found that gender, age, A-value, and VAD at the operculum were statistically significant (-Value = 0.003, <0.001, 0.031, and 0.027, respectively) by regression analysis. Moreover, we found that Age, H value, VAD at the midpoint, and VAD at the operculum were significant predictors of CT VAD volume (-Value < 0.04). Finally, gender (OR: 0.092; 95%CI: 0.009-0.982; -Value = 0.048) and VAD at the midpoint (OR: 0.106; 95%CI: 0.015-0.735; -Value = 0.023) were significant predictors of gusher risk. Patients' gusher risk was significantly differentiated by gender and VAD width at the midpoint.
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http://dx.doi.org/10.3390/jpm13020171 | DOI Listing |
Eur J Pediatr
September 2025
Department of Otolaryngology-Head and Neck Surgery, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230001, Anhui, China.
Unlabelled: Enlarged vestibular aqueduct (EVA) is one of the most common inner ear malformations (IEMs) leading to hearing loss in children. Although its genetic and clinical characteristics have been studied, its manifestations in completely deaf children in China, especially those with or without incomplete partition type II (IP-II), are not yet fully understood. We conducted a comprehensive analysis of 123 pediatric EVA children with complete hearing loss.
View Article and Find Full Text PDFJ Med Case Rep
August 2025
Otolaryngology Head and Neck Surgery, Jiujiang University Affiliated Hospital, Jiujiang, Jiangxi, The People's Republic of China.
Background: Branchio-oto-renal syndrome is a rare autosomal dominant disorder characterized by branchial arch anomalies, hearing loss, and renal dysplasia. Its diagnosis remains challenging due to clinical heterogeneity and overlapping features with other syndromes. This case report aims to enhance awareness of branchio-oto-renal syndrome and highlight multidisciplinary management strategies.
View Article and Find Full Text PDFLaryngoscope Investig Otolaryngol
August 2025
Objective: To clinically validate manual measurement of cochlear length from pre-operative image of cochlea with post-operative image of cochlear implant (CI) electrode.
Methods: Temporal bone computer tomography (CT) scans of 23 ears were available for this pilot study. The inner ear was three-dimensionally (3D) segmented, and cochlea length was manually measured for preferred angular depth depending on inner ear anatomical types for CI electrode length selection.
Diagn Cytopathol
October 2025
Department of Pathology and Laboratory Medicine, University of North Carolina Medical Center, Chapel Hill, North Carolina, USA.
Endolymphatic sac tumors are uncommon, slow growing, and locally aggressive neoplasms that arise within the endolymphatic sac, most commonly the intraosseous portion located in the temporal bone. There are only three previous cytology reports, and no prior FNAs have been reported. We present a case of a metastatic sporadic endolymphatic sac tumor, a phenomenon that has yet to be described on FNA and has only been previously reported once in cerebrospinal fluid cytology.
View Article and Find Full Text PDFJ Vestib Res
August 2025
Otology & Neurotology Group CTS495, Instituto de Investigación Biosanitaria, ibs.GRANADA, Granada, Spain.
PurposeTo estimate the prevalence of endolymphatic sac hypoplasia (EShp)-a proposed specific finding in Ménière's disease (MD) that defines an endophenotype characterized by bilateral involvement, male predominance, temporal bone abnormalities, and familial clustering-in individuals without MD, to assess its specificity for the condition.MethodsWe analyzed 956 temporal bone CT scans from individuals without MD to assess the prevalence of EShp using the Angular Trajectory of the Vestibular Aqueduct (ATVA) marker. ATVA distribution, reproducibility, and associations with clinical variables were also evaluated.
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