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Inflamed Symptomatic Sellar Arachnoid Cyst: Case Report
Article em En | WPRIM | ID: wpr-209505
Biblioteca responsável: WPRO
ABSTRACT
Sellar arachnoid cysts are rare; an infected arachnoid cyst is extremely rare as only one case has been reported to date in the literature. Here, we report a patient with an infected or inflamed sellar arachnoid cyst that was successfully treated with transsphenoidal surgery (TSA). A 53-year-old female with a history of chronic sinusitis developed a headache 5 months ago, and one month before admission polyuria, polydipsia, and abnormal vaginal bleeding occurred. The magnetic resonance imaging (MRI) showed a sellar cystic mass with a thickened pituitary stalk. Preoperative hormonal study revealed normal pituitary hormone levels except for a moderate elevation of prolactin. She was diagnosed with diabetes insipidus of the central nervous system origin based on a water-deprivation test. TSA was performed under an impression of symptomatic Rathke's cleft cyst according to the MRI findings. Intraoperative findings showed confirmation of turbid intracystic contents, but micro-organisms were unidentified on microbial culture. Pathology of the cyst wall revealed inflamed meningoepithelial lining cells compatible with an arachnoid cyst.
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Texto completo: 1 Índice: WPRIM Assunto principal: Patologia / Aracnoide-Máter / Hipófise / Poliúria / Prolactina / Sinusite / Hemorragia Uterina / Imageamento por Ressonância Magnética / Sistema Nervoso Central / Cistos Aracnóideos Tipo de estudo: Diagnostic_studies Limite: Female / Humans Idioma: En Revista: Brain Tumor Research and Treatment Ano de publicação: 2013 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Patologia / Aracnoide-Máter / Hipófise / Poliúria / Prolactina / Sinusite / Hemorragia Uterina / Imageamento por Ressonância Magnética / Sistema Nervoso Central / Cistos Aracnóideos Tipo de estudo: Diagnostic_studies Limite: Female / Humans Idioma: En Revista: Brain Tumor Research and Treatment Ano de publicação: 2013 Tipo de documento: Article