2019
DOI: 10.3171/2018.7.jns172501
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Neuroendoscopic fenestration of glioependymal cysts to the ventricle: report of 3 cases

Abstract: Glioependymal cysts are rare congenital lesions of the central nervous system. Reported surgical treatments of these lesions have varied and yielded mixed results, and the optimal surgical strategy is still controversial. The authors here report the clinical and surgical outcomes for three adult patients successfully treated with neuroendoscopic fenestration into the ventricular system. The patients had presented with symptomatic glioependymal cysts in the period from 2013 to 2016 at the authors’ institution. … Show more

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Cited by 7 publications
(17 citation statements)
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“…Histopathological analysis of the tumor is not necessary to make the diagnosis because the MRI radiological semiology of the lesion and its association with the abnormalities of the corpus callosum are sufficient to make this diagnosis [ 5 ].…”
Section: Discussionmentioning
confidence: 99%
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“…Histopathological analysis of the tumor is not necessary to make the diagnosis because the MRI radiological semiology of the lesion and its association with the abnormalities of the corpus callosum are sufficient to make this diagnosis [ 5 ].…”
Section: Discussionmentioning
confidence: 99%
“…The differential diagnoses of neuroglial cysts are arachnoid cyst, epidermoid cyst, ependymal cyst, and porencephalic cyst [ 5 ]: Arachnoid cyst typically presents as an unilocular extra-axial cystic lesion which has the same signal as CSF, its outlines are sharp and smooth, and it can displace or deform adjacent brain or adjacent calvarium (scalloping). The arachnoid cyst does not enhance [ 6 ] Epidermoid cysts appear as lobulated CFS-like mass that fills and expand CSF spaces and exerts a gradual mass effect, insinuating between structures and encasing adjacent nerves and vessels.…”
Section: Discussionmentioning
confidence: 99%
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“…Due to the rarity of this entity, the management is still unclear. Some authors support close follow-up in asymptomatic cases, 1,8,20 and others recommend surgical treatment in asymptomatic patients in case of significant ventricular enlargement 18 or in infants. 31 The most common approach is an open craniotomy with total or partial resection of the cyst wall, with or without a fenestration or shunting of the cyst into the ventricles or subarachnoid space.…”
Section: Discussionmentioning
confidence: 99%
“…[33][34][35][36][37] Likewise, a slow emptying of the cyst should be performed to prevent the sudden appearance of a space between the dura mater and the brain and to prevent the rapid decrease in intracranial pressure because both events can lead to the appearance of a subdural hematoma. These collections usually appear at the initial follow-up and do not usually require surgical intervention 1,8,38,39 The clinic usually subsides completely after surgery and the recurrence rate is low. However, patients must be closely followed over time.…”
Section: Discussionmentioning
confidence: 99%