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A Case of Aspergillus Clival Abscess Treated by Endoscopic Removal / 대한이비인후과학회지
Korean Journal of Otolaryngology - Head and Neck Surgery ; : 52-56, 2015.
Artículo en Coreano | WPRIM | ID: wpr-644372
ABSTRACT
Aspergillus clival abscess, especially without a sphenoid sinus lesion, is a very rare infection of central nervous system. In this report, we describe the successful treatment of a patient with aspergillus clival abscess. A 63-year-old man was referred to our hospital with the diagnosis of sphenoid mass lesion in magnetic resonance image accompanied by headache and diplopia. The computed tomography scan revealed a clival cystic lesion without connection with the sphenoid sinus. The patient underwent the endoscopic endonasal clival approach and histopathological examination revealed aspergillosis. Postoperatively, the patient was given IV amphotericin-B for 2 weeks and oral voriconazole for 3 months. After surgery, patient's headache and diplopia disappeared. Aspergillus abscess originating from the skull base is rare but has a high mortality rate. Histopathological confirmation via endonasal approach and intensive antifungal therapy should be started for a successful treatment.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Aspergilosis / Aspergillus / Seno Esfenoidal / Sistema Nervioso Central / Mortalidad / Base del Cráneo / Fosa Craneal Posterior / Diagnóstico / Absceso / Diplopía Tipo de estudio: Estudio diagnóstico / Estudio pronóstico Límite: Humanos Idioma: Coreano Revista: Korean Journal of Otolaryngology - Head and Neck Surgery Año: 2015 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Aspergilosis / Aspergillus / Seno Esfenoidal / Sistema Nervioso Central / Mortalidad / Base del Cráneo / Fosa Craneal Posterior / Diagnóstico / Absceso / Diplopía Tipo de estudio: Estudio diagnóstico / Estudio pronóstico Límite: Humanos Idioma: Coreano Revista: Korean Journal of Otolaryngology - Head and Neck Surgery Año: 2015 Tipo del documento: Artículo