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Vol. 62. Issue 6.
Pages 465-468 (November - December 2011)
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Vol. 62. Issue 6.
Pages 465-468 (November - December 2011)
Case study
Sensorineural Hearing Loss Evolution in Vogt–Koyanagi–Harada Syndrome
Evolución de la hipoacusia neurosensorial bilateral en el síndrome de Vogt Koyanagi Harada
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Verónica Rodríguez Riveraa,
Corresponding author
pecasve@hotmail.com

Corresponding author.
, Herminio Pérez Garriguesa, Roberto Gallego Pinazob
a Servicio de Otorrinolaringología, Hospital Universitario La Fe, Valencia, Spain
b Servicio de Oftalmología, Hospital Universitario La Fe, Valencia, Spain
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Table 1. Threshold Observed in the Audiometric Controls Conducted Throughout the Evolution (Days Elapsed from Diagnosis of the Disease).
Abstract

Vogt–Koyanagi–Harada syndrome is an autoimmune multisystem disease, characterized by the association of ocular inflammatory manifestations (uveitis and retinal detachment) and extraocular lesions such as meningismus and tegumentary or auditory findings. We report the case of a Hispanic woman with this syndrome.

Keywords:
Vogt–Koyanagi–Harada
Sensorineural hearing loss
Immunosuppressive treatment
Resumen

El síndrome de Vogt Koyanagi Harada corresponde a una enfermedad autoinmune multisistémica que se caracteriza por la asociación de manifestaciones inflamatorias oculares (uveítis, desprendimiento de retina) y lesiones extraoculares como meningismo, afectación dérmica y afectación del VIII par craneal. Presentamos el caso de una mujer hispana con este síndrome.

Palabras clave:
Vogt Koyanagi Harada
Hipoacusia neurosensorial
Tratamiento inmunosupresor

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