Intralabyrinthine neurinoma: Management, exeresis and auditory restoration with cochlear implant.

BACKGROUND AND OBJECTIVE: Vestibular schwannoma is a benign tumour that originates in the eighth cranial nerve. It is termed intralabyrinthine schwannoma (ILS) when it develops in the inner ear, this being a rare origin. We present our experience in the management of three patients with ILS. MATERIALS AND METHODS: The results of tumour excision and cochlear implantation were evaluated in three patients with ILS: two intracochlear schwannomas (ICS) and one intravestibular schwannoma (IVS). RESULTS: Prior to surgery, all patients presented progressive sensorineural hearing loss and tinnitus. Complete tumour resection and cochlear implantation was possible in all patients, with favourable hearing rehabilitation. CONCLUSIONS: The therapeutic approach will depend on tumour size, growth rate, degree of hearing loss and presence of vestibular symptoms. Cochlear implantation (CI) in patients with ILS is possible when the cochlear nerve is present and functional. CI in patients, whether or not preceded by tumour excision, is an option with good hearing results in selected patients.

Neurinoma intralaberíntico: manejo, exéresis y restauración auditiva con implante coclear / Intralabyrinthine neurinoma: Management, exeresis and auditory restoration with cochlear implant

Introducción y objetivo: El schwannoma vestibular es un tumor benigno que se origina en el octavo par craneal. Se denomina schwannoma intralaberíntico (SIL) cuando se origina en el oído interno, siendo este origen poco frecuente. Presentamos nuestra experiencia en el manejo de 3 pacientes con SIL.Material y métodosLos resultados de la exéresis tumoral e implantación coclear fueron evaluados en 3 pacientes con SIL: 2 casos de schwannoma intracoclear y un caso de schwannoma intravestibular.ResultadosPrevio a la cirugía, todos los pacientes presentaban hipoacusia neurosensorial progresiva y acúfeno ipsilateral. La resección tumoral completa y la colocación de un implante coclear fue posible en todos los casos, con una rehabilitación auditiva favorable.ConclusionesLa actitud terapéutica dependerá del tamaño del tumor, el crecimiento, el grado de pérdida auditiva y los síntomas vestibulares. La implantación coclear en pacientes con SIL es posible cuando el nervio coclear está presente y es funcionante. El IC en el SIL, ya sea con exéresis previa o no del tumor, es una opción con buenos resultados auditivos en pacientes seleccionados. (AU)

Introduction and objective: Vestibular schwannoma is a benign tumour that originates in the eighth cranial nerve. It is termed intralabyrinthine schwannoma (ILS) when it develops in the inner ear, this being a rare origin. We present our experience in the management of three patients with ILS.Material and methodsThe results of tumour excision and cochlear implantation were evaluated in three patients with ILS: two intracochlear schwannomas (ICS) and one intravestibular schwannoma (IVS).ResultsPrior to surgery, all patients presented progressive sensorineural hearing loss and tinnitus. Complete tumour resection and cochlear implantation was possible in all patients, with favourable hearing rehabilitation.ConclusionsThe therapeutic approach will depend on tumour size, growth rate, degree of hearing loss and presence of vestibular symptoms. Cochlear implantation (CI) in patients with ILS is possible when the cochlear nerve is present and functional. CI in patients, whether or not preceded by tumour excision, is an option with good hearing results in selected patients. (AU)

Malformaciones del octavo par en niños / Malformation of the eighth cranial nerve in children

Introducción y objetivos: La prevalencia de la hipoacusia neurosensorial (HNS) congénita es aproximadamente de 1,5-6 de cada 1.000 nacimientos. La disfunción del nervio auditivo (neuropatía auditiva) puede estar presente hasta en el 1-10% de los casos de HNS en niños, siendo menos frecuentes aquellas pérdidas debidas a una aplasia o hipoplasia del nervio auditivo. Los objetivos del estudio son describir la clínica, umbrales auditivos y etiología en una muestra de niños con HNS y aplasia o hipoplasia del octavo par. Metodología: Presentamos 34 niños (edad media 20 meses) con malformación del nervio auditivo e HNS profunda de una muestra de 385 niños implantados en los últimos 10 años. Estudiamos las características demográficas, clínicas y malformaciones asociadas (clasificaciones de Casselman y Sennaroglu). Los datos fueron procesados usando un análisis estadístico descriptivo bivariante (p<0,05). Resultados: Un 58,8% fueron bilaterales (IIa/IIa y I/I fueron los más frecuentes). De los unilaterales el IIb fue el más frecuente. La sensibilidad del cribado auditivo fue de un 77,4%. Encontramos diferencias estadísticamente significativas entre el grado de hipoacusia y los distintos tipos de aplasia (clasificación de Casselman). La sensibilidad de la TC fue del 46,3% y la especificidad del 85,7%. La RNM fue la prueba de imagen más sensible. Conclusiones: Un 10% de los niños en estudio para un implante coclear tienen una aplasia o hipoplasia del nervio auditivo. El grado de pérdida auditiva está directamente relacionado con los distintos tipos de aplasia (clasificación de Casselman). Aunque la TC y la RNM son complementarias, la RNM es el test de elección para la detección de malformaciones del nervio auditivo (AU)

Introduction and objectives: Prevalence of congenital sensorineural hearing loss (SNHL) is approximately 1.5-6 in every 1,000 newborns. Dysfunction of the auditory nerve (auditory neuropathy) may be involved in up to 1%-10% of cases; hearing losses because of vestibulocochlear nerve (VCN) aplasia are less frequent. The objectives of this study were to describe clinical manifestations, hearing thresholds and aetiology of children with SNHL and VCN aplasia. Methodology: We present 34 children (mean age 20 months) with auditory nerve malformation and profound HL taken from a sample of 385 children implanted in a 10-year period. We studied demographic characteristics, hearing, genetics, risk factors and associated malformations (Casselman's and Sennaroglu's classifications). Data were processed using a bivariate descriptive statistical analysis (P<.05). Results: Of all the cases, 58.8% were bilateral (IIa/IIa and I/I were the most common). Of the unilateral cases, IIb was the most frequent. Auditory screening showed a sensitivity of 77.4%. A relationship among bilateral cases and systemic pathology was observed. We found a statistically significant difference when comparing hearing loss impairment and patients with different types of aplasia as defined by Casselman's classification. Computed tomography (CT) scan yielded a sensitivity of 46.3% and a specificity of 85.7%. However, magnetic resonance imaging (MRI) was the most sensitive imaging test. Conclusions: Ten percent of the children in a cochlear implant study had aplasia or hypoplasia of the auditory nerve. The degree of auditory loss was directly related to the different types of aplasia (Casselman's classification) Although CT scan and MRI are complementary, the MRI is the test of choice for detecting auditory nerve malformation (AU)

Malformation of the eighth cranial nerve in children. / Malformaciones del octavo par en niños.

INTRODUCTION AND OBJECTIVES: Prevalence of congenital sensorineural hearing loss (SNHL) is approximately 1.5-6 in every 1,000 newborns. Dysfunction of the auditory nerve (auditory neuropathy) may be involved in up to 1%-10% of cases; hearing losses because of vestibulocochlear nerve (VCN) aplasia are less frequent. The objectives of this study were to describe clinical manifestations, hearing thresholds and aetiology of children with SNHL and VCN aplasia. METHODOLOGY: We present 34 children (mean age 20 months) with auditory nerve malformation and profound HL taken from a sample of 385 children implanted in a 10-year period. We studied demographic characteristics, hearing, genetics, risk factors and associated malformations (Casselman's and Sennaroglu's classifications). Data were processed using a bivariate descriptive statistical analysis (P<.05). RESULTS: Of all the cases, 58.8% were bilateral (IIa/IIa and I/I were the most common). Of the unilateral cases, IIb was the most frequent. Auditory screening showed a sensitivity of 77.4%. A relationship among bilateral cases and systemic pathology was observed. We found a statistically significant difference when comparing hearing loss impairment and patients with different types of aplasia as defined by Casselman's classification. Computed tomography (CT) scan yielded a sensitivity of 46.3% and a specificity of 85.7%. However, magnetic resonance imaging (MRI) was the most sensitive imaging test. CONCLUSIONS: Ten percent of the children in a cochlear implant study had aplasia or hypoplasia of the auditory nerve. The degree of auditory loss was directly related to the different types of aplasia (Casselman's classification) Although CT scan and MRI are complementary, the MRI is the test of choice for detecting auditory nerve malformation.

Papel de la resonancia magnética de difusión en el diagnóstico y seguimiento del colesteatoma. Estudio con la técnica PROPELLER difusión / The role of diffusion-weighted magnetic resonance imaging in cholesteatoma diagnosis and follow-up. Study with the diffusion PROPELLER technique

Introducción y objetivos: El diagnóstico del colesteatoma se basa en los hallazgos clínicos y en la tomografía computarizada. Actualmente, con las nuevas técnicas de resonancia magnética potenciada en difusión no ecoplanares, sin necesidad de contraste intravenoso, es posible diferenciar entre colesteatoma y tejido de granulación o inflamatorio. Por ello, esta técnica muestra su máxima utilidad en la valoración de recidivas de colesteatoma tras timpanoplastias, sobre todo en técnicas cerradas, ya que puede evitar un alto porcentaje de cirugías de revisión. Otras indicaciones de la técnica son los casos de diagnóstico complejo y el colesteatoma congénito. El objetivo de este estudio es valorar la validez (sensibilidad y especificidad) y la seguridad (valor predictivo positivo y valor predictivo negativo) de la secuencia de difusión PROPELLER, una de las técnicas potenciada en difusión no ecoplanar en el diagnóstico del colesteatoma. Métodos: Estudio prospectivo de 52 pacientes con sospecha de colesteatoma en el que se correlacionan hallazgos clínicos y quirúrgicos con los obtenidos del estudio de resonancia magnética, que incluía una secuencia potenciada en difusión no ecoplanar (PROPELLER) de oídos. Resultados: La sensibilidad de la prueba para el grupo fue del 92,85%, la especificidad del 92,30%, el valor predictivo positivo del 92,85% y el valor predictivo negativo del 92,30%. Conclusiones: La resonancia magnética con imagen potenciada en difusión no ecoplanar utilizando la secuencia PROPELLER, es una técnica eficaz en el control del colesteatoma, permitiendo diagnosticar lesiones mayores de 2mm(AU)

Introduction and objectives: The diagnosis of cholesteatoma is based on clinical evaluation and computed tomography. New non-echo-planar diffusion-weighted magnetic resonance imaging (MRI) techniques, without intravenous contrast, are capable of differentiating cholesteatoma from inflammatory tissue, cholesterol granuloma and granulation tissues. The technique is very helpful in differential diagnosis of cholesteatoma, mainly after canal wall-up tympanoplasty surgery, to avoid routine second-look surgery in these patients. Congenital cholesteatoma and difficult cases can be detected and correctly diagnosed as well. The aim of this study was to evaluate sensitivity, specificity, positive predictive value and negative predictive value of the diffusion-weighted PROPELLER MRI in cholesteatoma diagnosis. Methods: A prospective study was performed on 52 patients. Clinical and surgical findings were correlated with diffusion-weighted PROPELLER MRI results. Results: Sensitivity, specificity and positive and negative predictive values were 92.85%, 92.30, 92.85 and 92.30%, respectively. Conclusions: Diffusion-weighted PROPELLER imaging is an effective technique in cholesteatoma diagnosis. It is capable of detecting lesions larger than 2mm(AU)

The role of diffusion-weighted magnetic resonance imaging in cholesteatoma diagnosis and follow-up. Study with the diffusion PROPELLER technique.

INTRODUCTION AND OBJECTIVES: The diagnosis of cholesteatoma is based on clinical evaluation and computed tomography. New non-echo-planar diffusion-weighted magnetic resonance imaging (MRI) techniques, without intravenous contrast, are capable of differentiating cholesteatoma from inflammatory tissue, cholesterol granuloma and granulation tissues. The technique is very helpful in differential diagnosis of cholesteatoma, mainly after canal wall-up tympanoplasty surgery, to avoid routine second-look surgery in these patients. Congenital cholesteatoma and difficult cases can be detected and correctly diagnosed as well. The aim of this study was to evaluate sensitivity, specificity, positive predictive value and negative predictive value of the diffusion-weighted PROPELLER MRI in cholesteatoma diagnosis. METHODS: A prospective study was performed on 52 patients. Clinical and surgical findings were correlated with diffusion-weighted PROPELLER MRI results. RESULTS: Sensitivity, specificity and positive and negative predictive values were 92.85%, 92.30, 92.85 and 92.30%, respectively. CONCLUSIONS: Diffusion-weighted PROPELLER imaging is an effective technique in cholesteatoma diagnosis. It is capable of detecting lesions larger than 2mm.