scholarly journals Intrasphenoidal Rathke’s Cleft Cyst: Case presentation and review of the literature

2016 ◽  
Vol 30 (4) ◽  
pp. 520-525 ◽  
Author(s):  
Umit Kocaman ◽  
Muhammet Bahadir Yilmaz ◽  
Hakan Yilmaz

Abstract Rathke’s cleft cyst is a benign lesion of embryological origin with sellarsuprasellar localization. It is found in 12-33% of normal pituitary glands in autopsy series. Although it is mostly asymptomatic, it can cause symptoms by compressing surrounding neural and pituitary tissues. The most common symptoms are endocrine problems, visual problems and headache. Uncommonly, the lesion can present with apoplexy. It is rarely reported outside sellar-suprasellar sites, such as the cerebellopontine angle, prepontine cistern, and intrasphenoidal locations. We present an intrasphenoidal Rathke’s cleft cyst found during investigation of a headache and operated on. We discussed the case with literature review and two similar reported cases.

Pituitary ◽  
2021 ◽  
Author(s):  
F. Aranda ◽  
R. García ◽  
F. J. Guarda ◽  
F. Nilo ◽  
J. P. Cruz ◽  
...  

2001 ◽  
Vol 8 (6) ◽  
pp. 564-567 ◽  
Author(s):  
Markus Wenger ◽  
Marian Simko ◽  
Regula Markwalder ◽  
Ethan Taub

2017 ◽  
Vol 20 (5) ◽  
pp. 480-484 ◽  
Author(s):  
Takamasa Kamei ◽  
Masahiro Nonaka ◽  
Yoshiko Uemura ◽  
Yasuo Yamanouchi ◽  
Yumiko Komori ◽  
...  

Rathke’s cleft cyst is a cystic disease that occurs in the sella turcica or, occasionally, in the suprasellar area. An ectopic Rathke’s cleft cyst is extremely rare, and its nature is less well understood. The authors report the case of a 14-year-old girl who presented with a growing cystic lesion in the prepontine cistern, immediately behind the dorsum sellae. Preoperative imaging and intraoperative investigation showed part of the cyst wall continuing into the dorsum sellae, to the pituitary gland. The cisternal portion of the cyst wall was totally resected via a right subtemporal approach. Histopathological examination of the cyst wall showed a monolayer of ciliated cells, identical to those of Rathke’s cleft cyst. To the best of the authors’ knowledge, this represents the first pediatric case of Rathke’s cleft cyst occurring in the prepontine cistern.


2021 ◽  
Vol 12 ◽  
Author(s):  
Shenzhong Jiang ◽  
Zhaojian Wang ◽  
Yan You ◽  
Renzhi Wang ◽  
Xinjie Bao

In this article, we present a 31-year-old female who presented with intermittent headache and oligomenorrhea of over 10 years’ duration. Imaging revealed a large suprasellar mass with sellar extension. The patient underwent an endoscopic endonasal trans-sphenoidal surgery to resection of the mass. Clinical, radiological, and operative findings from this patient were initially considered to be Rathke’s cleft cyst (RCC). However, postoperative histological examinations revealed a mature cystic teratoma. No radiotherapy was performed after surgery. At the most recent follow-up, approximately 1 year later, the patient is doing well with no headache and no recurrence of the teratoma.


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