scholarly journals Recurrent Lateral Ventricular Enterogenous Cyst: A Report of an Extreme Rare Case

2017 ◽  
Vol 2017 ◽  
pp. 1-4
Author(s):  
Md. Shamsuzzaman Mondle ◽  
Md. Shamsul Alam ◽  
Misbah Uddin Ahmad ◽  
Md. Abdullah Yusuf

The patient was a 45-year-old man with a progressive headache. Evaluation in detail revealed it as a case of left lateral ventricular space occupying lesion (SOL) resembling choroid plexus papilloma. A left parietal craniotomy was done and the lesion was removed completely through intraparietal approach. Surgical removal resulted in complete symptomatic relief. Histopathology revealed that it was a case of the enterogenous cyst. One year after surgery, the patient again experienced the same symptom and the images revealed recurrence of the lesion. The patient has undergone 2nd surgery and histopathology was the same as before. The patient was given radiotherapy and now he is completely relieved and well. Although intracranial enterogenous cyst is not uncommon, intraventricular enterogenous cyst as well as recurrent intraventricular enterogenous cyst is a rare entity.

2021 ◽  
Vol 20 (4) ◽  
pp. 33-41
Author(s):  
A. F. Valiakhmetova ◽  
L. I. Papusha ◽  
A. V. Sanakoeva ◽  
L. V. Shishkina ◽  
O. I. Budanov ◽  
...  

Choroid plexus tumors (CPTs) are rare intraventricular tumors, accounting 2–5% of brain tumors in children. Choroid plexus papilloma (CPP) classified by the World Health Organization (WHO) on the basis of histological criteria as benign tumor (WHO grade I), CPPs accounts for 10–20% of brain tumors during the first year of life, the median age of patients with CPP at the time of diagnosis – 3.5 years. Atypical choroid plexus papilloma (APP) is an intermediate (WHO grade II) tumor which was officially included in the WHO classification in 2007. Median age 0,63 years. In this work, for the first time in the Russian literature, we present the outcomes of CPP and APP therapy in a large cohort of patients. The study was approved by the Independent Ethics Committee and the Scientific Council of the D. Rogachev NMRCPHOI. In our study from January 1, 2009 to December 31, 2019, 83 CPP and 37 APP were histologically verified. For all patients, surgical removal of the tumor was the first stage of treatment. In 79 (95.2%) patients with CPP and in 32 (86.5%) children with APP, radical resection was performed at the first stage. In 73.5% of children with CPP and 62.2% of children with APP there was no intra- and postoperative complications. In both CPP and APP, the 5-year EFS in patients with complete resection was statistically significantly higher compared to subtotal tumor resection (100% and 33 ± 27% in CPP, 94 ± 4% and 25 ± 22% for APP) (p < 0.001). Chemoradiation therapy was given to 1 patient with CPP, 4 patients with APP with tumor recurrence/progression. 


Cureus ◽  
2020 ◽  
Author(s):  
Mohammed Hamza Shah ◽  
Mohamed Abdelhady ◽  
Ahmed Own ◽  
Ahmed Elsotouhy

2020 ◽  
Vol 3 (1(January-April)) ◽  
pp. e632020
Author(s):  
Marcos Rodrigo Pereira Eismann ◽  
Antônio Cesar De Mello Mussi

A 12 year-old boy with headaches for 2 months. Magnetic resonance imaging of the brain found a small lesion in the atrium of the right lateral ventricle. We show a posterior interhemispheric approach to the ventricular atrium through a corticotomy in the pre-cuneus and the posterior cingulate gyrus. This approach has the advantage of avoiding lesion to the optic radiation. A complete resection of the lesion was performed without complications. Anatomopathological result showed choroid plexus papilloma. This benign tumor corresponds to less than 1% of brain tumors and typically presents with signs of intracranial hypertension with hydrocephalus.


1994 ◽  
Vol 30 (4) ◽  
pp. 643
Author(s):  
Joo Hyeong Oh ◽  
Tae Hoon Kim ◽  
Woo Suk Choi

2008 ◽  
Vol 15 (6) ◽  
pp. 708-712 ◽  
Author(s):  
H. Akil ◽  
N.J. Coupe ◽  
J. Singh

2015 ◽  
Vol 32 (4) ◽  
pp. 717-721 ◽  
Author(s):  
Gustavo S. Jung ◽  
Leonardo G. Ruschel ◽  
Andre G. Leal ◽  
Ricardo Ramina

Neurosurgery ◽  
1983 ◽  
Vol 12 (2) ◽  
pp. 217???20 ◽  
Author(s):  
W C Gradin ◽  
C Taylon ◽  
A H Fruin

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