A unique case of Central Neurocytoma and concomitant brain AVM in a 12-year-old girl with long term follow up and review of the literature

•The first case of concurrent CNCy and Bari AVM, SM3 is reported.•Even though this may be a coincidence but further research regarding the pathophysiology of such a combination is warranted.•Close follow-up and on-time intervention may help to achieve a better outcome. Central Neurocytoma (CNCy) is...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Interdisciplinary neurosurgery : Advanced techniques and case management 2024-06, Vol.36, p.101962, Article 101962
Hauptverfasser: Amirjamshidi, Abbas, Abbasioun, Kazem, Babak Ghasemi, Seyed
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•The first case of concurrent CNCy and Bari AVM, SM3 is reported.•Even though this may be a coincidence but further research regarding the pathophysiology of such a combination is warranted.•Close follow-up and on-time intervention may help to achieve a better outcome. Central Neurocytoma (CNCy) is an exceedingly rare brain tumor occurring within the ventricles in young adults. Anecdotal cases of CNCy occurring simultaneously with other brain lesions have been reported but to the best of our knowledge, no one was accompanied by brain AVM. Case presentation: A 12-year-old girl presented with signs of increased intracranial pressure. A multi-bleb CNCy originated from the septum in the midline, expanding to the lateral and third ventricles, back to the incisura and infratentorial- supra-cerebellar cistern concomitant with a left frontal parafalx AVM. The tumor excised successfully, and hydrocephalus controlled by ventriculoperitoneal shunting. The AVM bled after 7 years and was removed surgically. She is tumor free after 10 years. We present the first case of CNCy concomitant with brain AVM in a 12-year-old girl with more than 10 years follow up.
ISSN:2214-7519
2214-7519
DOI:10.1016/j.inat.2024.101962