MRI of Symptomatic Rathke's Cleft Cyst : MR Intensity of Cyst Contents and Clinical Manifestations
نویسندگان
چکیده
منابع مشابه
Symptomatic Rathke's cleft cyst.
A rare case of symptomatic Rathke's cleft cyst in a 26-year-old female is reported. The clinical and radiological features of this lesion are described with emphasis on the differential diagnosis between Rathke's cleft cyst and craniopharyngIOma. Rathke's cleft cysts present a common incidental intrasellar autopsy finding occurring in 13% to 22% of randomly examined pituitary glands [1]. These ...
متن کاملSymptomatic Rathke's Cleft Cyst
=Abstract=The first Korean case of a symptomatic Rathke's cleft cyst in a 14-year old boy is described. His chief complaint was headache of 2 months' duration and he had diabetes insipidus, hypopituitarism and decreased visual acuity on both sides. The computerized tomography scannng revealed an isodense small round mass at the suprasellar cistern with partial enhancement. The cyst was removed ...
متن کاملSYMPTOMATIC RATHKE\'S CLEFT CYST: A CASE REPORT
A large Rathke's cyst was marsupialized into the sphenoid sinus of a 45-year old woman who presented with headache, polydipsia, cessation of menses and diplopia. A brief review of cases is presented.
متن کاملSymptomatic Rathke’s Cleft Cyst Presenting With Decreased Visual Acuity
Background and Importance: Symptomatic Rathke’s cleft cyst is a rare lesion that often presents without any symptoms. Case Presentation: We report a 40-year-old female with symptomatic Rathke’s cleft cyst located in the sellar and suprasellar region. She presented with visual disturbance, headache, weight gain, hypothyroidism and amenorrhea. The patient underwent surgery and ...
متن کاملSymptomatic Rathke's cleft cyst. Case report.
A case of a symptomatic Rathke's cleft cyst in a 10-year-old boy is described. The importance of the intraoperative differentiation between this rare tumor and a craniopharyngioma is discussed.
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ژورنال
عنوان ژورنال: Japanese Journal of Neurosurgery
سال: 1997
ISSN: 0917-950X,2187-3100
DOI: 10.7887/jcns.6.448