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Inflamed Symptomatic Sellar Arachnoid Cyst: Case Report
Brain Tumor Research and Treatment ; : 28-31, 2013.
Artículo en Inglés | WPRIM | ID: wpr-209505
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: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Aracnoides / Hipófisis / Poliuria / Prolactina / Sinusitis / Hemorragia Uterina / Imagen por Resonancia Magnética / Sistema Nervioso Central / Quistes Aracnoideos Tipo de estudio: Estudio diagnóstico Límite: Femenino / Humanos Idioma: Inglés Revista: Brain Tumor Research and Treatment Año: 2013 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Aracnoides / Hipófisis / Poliuria / Prolactina / Sinusitis / Hemorragia Uterina / Imagen por Resonancia Magnética / Sistema Nervioso Central / Quistes Aracnoideos Tipo de estudio: Estudio diagnóstico Límite: Femenino / Humanos Idioma: Inglés Revista: Brain Tumor Research and Treatment Año: 2013 Tipo del documento: Artículo