scholarly journals Cushing's Syndrome in a Patient With Rathke's Cleft Cyst and ACTH Cell Hyperplasia Detected by 11C-Methionine PET Imaging—A Case Presentation

2020 ◽  
Vol 11 ◽  
Author(s):  
Karol Piotr Sagan ◽  
Elzbieta Andrysiak-Mamos ◽  
Leszek Sagan ◽  
Przemysław Nowacki ◽  
Bogdan Małkowski ◽  
...  
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.


2016 ◽  
Vol 13 (4) ◽  
pp. 45-48
Author(s):  
Svetlana Vorotnikova ◽  
Larisa Dzeranova ◽  
Ekaterina Pigarova ◽  
Aleksander Vorontsov ◽  
Viktoriya Vladimirova ◽  
...  

Rathke’s cleft cyst is one of the causes of hyperprolactinemia. It forms due to pituitary malformation during embryonic period. Nowadays the correct diagnosis still possesses some issues with interpretation of visual data and variable clinical picture. The article presents a clinical case of a patient with Rathke’s cleft cyst that was initially managed as prolactinoma.


2018 ◽  
Author(s):  
Ines Barka ◽  
Faiza Bensmaine ◽  
Moctar Bah ◽  
Clara Bouche ◽  
Jean Francois Gautier

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

Author(s):  
Rebecca Limb ◽  
James King

Abstract Study Objective The main purpose of this article is to address the question of whether reconstructing the sellar floor following Rathke's cleft cyst excision results in increased rates of recurrence. Methods and Design A retrospective case series was compiled from medical records and radiological investigations at a single institution over a time period spanning 25 years. Episodes of cyst recurrence were determined from magnetic resonance imaging scans and outpatient encounters. Details regarding surgical procedure and techniques were obtained from operation notes. Perioperative morbidity was also recorded. Results Twenty-three adult patients were treated surgically for a Rathke's cleft cyst at the study institution between 1992 and 2017. The overall cyst recurrence rate was 48%, with 39% of all patients requiring redo surgery within the timeframe of the study. The mean time to redo surgery for recurrence was 4 years. Cyst recurrence rates were 57% postmicroscopic procedures, and 26% postendoscopic procedures (p = 0.148). In the nonreconstructed group, the recurrence rate was 17%, and in the reconstructed group the recurrence rate was 41% (p = 0.3792). Complications arising after nonreconstructive procedures were delayed cerebrospinal fluid rhinorrhea, pneumocephaly, and multiple episodes of meningitis. All these patients required return to theater for secondary reconstruction of the pituitary fossa floor. Conclusion The results of this small study suggest that reconstruction of the sellar floor, and microscopic rather than endoscopic techniques, may be associated with a higher rate of Rathke's cleft cyst recurrence. However, these trends did not reach statistical significance. Patients undergoing nonreconstructive procedures may be more prone to certain postoperative complications.


1999 ◽  
Vol 141 (10) ◽  
pp. 1055-1061 ◽  
Author(s):  
N. Saeki ◽  
K. Sunami ◽  
Y. Sugaya ◽  
A. Yamaura

1996 ◽  
Vol 37 (3P2) ◽  
pp. 596-598 ◽  
Author(s):  
K. Skjødt ◽  
A. Loft Edal ◽  
H. J. Nepper-Rasmussen

Two patients with Rathke's cleft cyst with uncommon MR signals, hyperintensity on T1-weighted, and hypointensity on T2-weighted 3-D fast field echo (FFE) imaging are reported. We suggest that this is due to high content of cholesterol or mucopolysaccharide, possibly combined with cell debris from the cyst wall.


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