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Inflamed Symptomatic Sellar Arachnoid Cyst: Case Report
Brain Tumor Research and Treatment ; : 28-31, 2013.
Article in English | 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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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Arachnoid / Pituitary Gland / Polyuria / Prolactin / Sinusitis / Uterine Hemorrhage / Magnetic Resonance Imaging / Central Nervous System / Arachnoid Cysts Type of study: Diagnostic study Limits: Female / Humans Language: English Journal: Brain Tumor Research and Treatment Year: 2013 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Arachnoid / Pituitary Gland / Polyuria / Prolactin / Sinusitis / Uterine Hemorrhage / Magnetic Resonance Imaging / Central Nervous System / Arachnoid Cysts Type of study: Diagnostic study Limits: Female / Humans Language: English Journal: Brain Tumor Research and Treatment Year: 2013 Type: Article