An elusive pelvic cyst: a case report of an anterior sacral meningocele

2007 ◽  
Vol 5 (2) ◽  
pp. 147-150
Author(s):  
K. Johnston ◽  
N. Y. J. Ji ◽  
D. Chou ◽  
M. Davies ◽  
A. Chai ◽  
...  
2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Mehmet Beyazal

Anterior sacral meningocele is characterized by herniation of the meningeal sac due to a developmental bone defect in the front of a sacrum bone. It was first described in 1837. The sacral meningocele may be congenital or acquired. It is usually discovered during a rectal or pelvic examination as a cystic lesion or discovered incidentally. Most of the symptoms are due to compression on the adjacent organs. In this paper, we present a case of an asymptomatic female patient who had a pelvic cyst detected during a routine obstetric ultrasound examination. We show radiological findings of the detailed postpartum evaluation of the cyst, which led to detection of sacral agenesis, huge anterior sacral meningocele, and significant arcuate uterus.


Author(s):  
Eissa Ahmed Ibrahim ◽  
Mohamad Motawea ◽  
Ahmed M. Abd El-khalek ◽  
Khaled Zaghloul ◽  
Mohamad Samy

Neurosurgery ◽  
1990 ◽  
Vol 27 (6) ◽  
pp. 981-986 ◽  
Author(s):  
Richard B. North ◽  
David H. Kidd ◽  
Henry Wang

Abstract None of the more than 180 cases of anterior sacral meningocele reported in the past 150 years has been bilateral, and only two have been associated with occult intrasacral meningocele. We report a unique case of bilateral anterior sacral cysts, communicating with the subarachnoid space, associated with occult intrasacral meningeal and perineurial (Tarlov's) cysts, in an asymptomatic woman. The pertinent clinical and diagnostic imaging literature is reviewed.


2015 ◽  
Vol 11 (02) ◽  
pp. 141-145
Author(s):  
Manoranjan Mohapatra ◽  
Dina Satpathy ◽  
Swarnalata Das ◽  
Aswini Mohanty ◽  
Sibabratta Patnaik

Neurosurgery ◽  
1988 ◽  
Vol 22 (3) ◽  
pp. 581-588 ◽  
Author(s):  
Massimo S. Fiandaca ◽  
Wayne K. Ross ◽  
Gary S. Pearl ◽  
Roy A.E. Bakay

Abstract We report a case of a presacral teratoma containing a malignant carcinoid component associated with an anterior sacral meningocele that presented in a 35-year-old woman. The clinical, radiographic, and pathological features of these rare tumors, of presacral meningoceles, and of the hereditary presacral teratoma syndrome are discussed. (Neurosurgery 22:581-588, 1988)


Sign in / Sign up

Export Citation Format

Share Document