Symptomatic Rathke’s Cleft Cyst Presenting With Decreased Visual Acuity

Authors

  • Elena Jamali Department of Neurosurgery, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Guive Sharifi Department of Neurosurgery, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • karim Moradian Kokhdan Department of Neurosurgery, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Kaveh Ebrahim Zadeh Department of Neurosurgery, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Mohammad Samadian Department of Neurosurgery, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Omidvar Rezaee Department of Neurosurgery, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Saeed Razmeh Department of Neurology, School of Medicine, Yasuj University of Medical Sciences, Yasuj, Iran.
  • Shahram Sabeti Department of Neurosurgery, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:

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 the pathological examination confirmed Rathke’s cleft cyst. Conclusion: Although the symptomatic Rathke’s cleft cyst is rare, the differential diagnosis must be done with intrasellar and suprasellar lesions.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

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 ...

full text

Symptomatic 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 ...

full text

Symptomatic Rathke's cleft cyst with amyloid stroma.

A patient with panhypopituitarism and visual field defects due to a Rathke's cleft cyst is presented. These cysts are commonly found in random pituitaries examined at necropsy, but rarely produce symptoms. Subtle endocrine deficiencies, however, may now be uncovered more frequently with modern diagnostic techniques. An unusual and unreported feature of this cyst was an apudamyloid stroma. This ...

full text

SYMPTOMATIC 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.

full text

A Rathke's Cleft Cyst Presenting with Apoplexy

The occurrence of symptomatic pituitary hemorrhage into a Rathke's cleft cyst (RCC) is extremely rare. The author reports an interesting case of intra- and suprasellar RCC presented with features of pituitary apoplexy. This 62-year-old woman suffered acute headache, mental confusion, and partial hypopituitarism. The characteristics of the magnetic resonance imaging seemed most compatible with a...

full text

Symptomatic 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.

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 3  issue None

pages  165- 168

publication date 2018-01

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023