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A 30-year-old man presented with minute-long episodes of vertigo and severe autophony. CVEMP showed a decreased threshold when testing the left side, potentially indicating SSCD. A subsequent MRI demonstrated a multi-lobulated, cystic mass in the temporal bone and the radiological diagnosis at that time was ELST. Tumor excision was performed, and microscopic examination of the excised material revealed fibrovascular tissue without signs of papillary or cystic projections. The conclusion of the histological assessment rendered a diagnosis of angiofibroma. We were unable to find a previous report of ENA originating around the endolymphatic sac. Laryngoscope, 134:1897-1900, 2024.

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Introducción: La dehiscencia del canal semicircular posterior es una vestibulopatía rara, de baja prevalencia y cuya sintomatología se explica por el fenómeno de la tercera ventana. No fue hasta 2003 cuando Krombach describe los primeros casos. Objetivo: Evaluar mediante análisis bibliométrico y temático la producción científica sobre trabajos de dehiscencia del canal semicircular posterior (DCSP) y su incidencia a nivel de la comunidad científica mediante una revisión bibliográfica. Método: Se realiza búsqueda, revisión, selección y estudio a partir de ítems relacionados con DCSP indexados en la base de datos Pubmed, Web of Science, Alcorze y Scopus, desde el año 2003 hasta 2019, seleccionando 90 artículos. Resultados: Los 90 artículos han sido publicados en un total de 48 revistas, siendo 52% originales, 38% casos clínicos, 9% revisiones y 1% conferencias. La temática predominante fue la clínica (32%) y la etiología (27%). Los artículos estaban escritos en ocho idiomas diferentes, predominando el inglés (85%), y siendo Estados Unidos el país con más publicaciones (42%). Los índices de actividad institucional y autoría son bajos. La calidad de las revistas es alta, ya que el 70% de las publicaciones se encontraban en los cuartiles Q1-Q2. El área principal es Otorrinolaringología, con 66 trabajos, seguida por Radiología con 14. El número de descargas fue 6958, con una media de 77,31 por artículo, y las citaciones fueron 1193, equivalente a una media de 13,25. Conclusión: Los datos bibliométricos revelan cómo los trabajos sobre dehiscencia del canal semicircular posterior representan una pequeña producción científica, el tema está en fase de crecimiento sostenido, los índices de autoría, institucionalidad y colaboración son bajos y las publicaciones se concentran en pocas revistas, con una orientación claramente anglófona, pero de alta calidad e importante visualización. (AU)

Introduction: The dehiscence of the posterior semicircular canal is a rare vestibulopathy, of low prevalence and whose symptomatology is explained by the phenomenon of the third window. It was not until 2003 that Krombach described the first cases. Objective: Evaluate the scientific production about the dehiscence of the posterior semicircular canal (DCSP) by a bibliometric and thematic analysis and observes its incidence at the scientific community level. Method: A search with subsequent review, selection and study was carried out using items related to DCSP indexed in the Pubmed, Web of Science, Alcorze and Scopus databases, from 2003 to 2019, selecting a total of 90 articles. Results: The 90 articles have been published in a total of 48 magazines. 52% were originals, 38% clinical cases, 9% reviews and 1% conferences. Clinical (32%) and etiology (27%) were the main themes. The articles were written in eight different languages, predominantly English (85%), and the United States has been the country with the highest number of publications (42%). Institutional activity and authorship rates are low. The quality of the journals is high: 70% of the publications were in the Q1-Q2 quartiles. The main area corresponds to otorhinolaryngology, with a total of 66 works, followed by radiology (14). The total number of downloads was 6958, with an average of 77.31 per article and the total citations were 1193, 13.25 per article. Conclusions: The bibliometric results reveal how the works on dehiscence of the posterior semicircular canal present a small scientific production, the subject is in a phase of sustained growth, the authorship, institutional and collaboration index are low, the publications are concentrated in a few journals of high quality and important visualization, with a clearly anglophone orientation. (AU)

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The objective of this study was to evaluate the characteristic symptoms of and treatments for lateral semicircular canal dehiscence (LSCD) and posterior semicircular canal dehiscence (PSCD) and its proposed mechanism. A dehiscence acquired in any of the semicircular canals may evoke various auditory symptoms (autophony and inner ear conductive hearing loss) or vestibular symptoms (vertigo, the Tullio phenomenon, and Hennebert sign) by creating a "third mobile window" in the bone that enables aberrant communication between the inner ear and nearby structures. A PubMed search was performed using the keywords lateral, posterior, and semicircular canal dehiscence to identify all relevant cases. Our data suggest that PSCD, although clinically rare, is most likely associated with a high-riding jugular bulb and fibrous dysplasia. Patients may experience auditory manifestations that range from mild conductive to extensive sensorineural hearing loss. LSCD is usually associated with chronic otitis media with cholesteatoma.

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OBJECTIVE: Establishing the prevalence of semicircular canal dehiscence in a pediatric population using temporal bone CT imaging. STUDY DESIGN: Retrospective analysis of all temporal bone CT scans during a 5-year period (2007-2012). METHODS: CT scan images were reformatted in the plane of the canals and assessed by two independent reviewers with a third to resolve disagreement. Detailed chart review was performed for those found to have dehiscence. Superior and posterior canals were classified as "dehiscent", "possibly dehiscent", "thin" or "normal" for each case. RESULTS: 649 temporal bones were assessed from 334 children (under 18 years of age). The prevalence rate of superior canal dehiscence (SCD) was 1.7% (3.3% of individuals). Posterior canal dehiscence (PCD) was present in 1.2% (2.1% of individuals). There were no cases of bilateral SCD, and one case of bilateral PCD. Age under 3 years was associated with a higher prevalence of thinning but not dehiscence. Congenital inner ear malformation was not related to a higher probability of dehiscence. The superior petrosal sinus was associated with the SCD in three cases (27.3%). Retrospective chart review highlighted possible vestibular symptoms in 3/11 patients with SCD (27.3%). CONCLUSIONS: This forms the largest pediatric study of canal dehiscence to date. This study's prevalence rate is significantly lower than previous reports. The identified association with overlying venous structures may reflect the etiological process involved. The occurrence in children supports the hypothesis of a congenital predisposition for development of canal dehiscence syndrome.

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We herein report a case of posterior semicircular canal dehiscence (SCD) syndrome who had been audiologically followed up for eight years. The patient originally had sensorineural hearing loss. The audiogram had gradually transformed to pure conductive hearing loss. The posterior SCD was identified in CT scan. The reported case showed the possibility to distinguish the mechanism at play underlying the typical conductive hearing loss in SCD patients by tracing the transition of the hearing loss pattern. This information is of much help to predict the hearing outcomes if surgical intervention were chosen for the treatment.

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Multiple semicircular canal dehiscences are clinical entities characterised by vestibular and cochlear symptoms induced by enhanced sensitivity of labyrinthine receptors due to a multiple bone defect of the otic capsule. The case is presented of a 38-year-old male with bilateral posterior semicircular canal dehiscence associated with unilateral (right) superior semicircular canal dehiscence. The man suffered from vestibular (recurrent Tullio Phenomenon or sound-induced vertigo) and cochlear symptoms (persistent aural fullness associated with mixed hearing loss and disabling tinnitus).

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