Pathological Changes in Surgically Resected Cystic Cerebral Cavernous Malformation 13 Years After Radiosurgery: Case Report and Review of the Literature

2020 ◽  
Vol 143 ◽  
pp. 392-397
Author(s):  
Chao Wang ◽  
Bing Yu ◽  
Fengyue Zhang ◽  
Kaijian Zheng ◽  
Yugong Feng
Keyword(s):  
Case Report ◽  
Cavernous Malformation ◽  
Cerebral Cavernous Malformation ◽  
Pathological Changes ◽  
Review Of The Literature

Giant cerebellar cavernous malformation in 4-month-old boy. Case report and review of the literature

2013 ◽  
Vol 47 (6) ◽  
pp. 595-600 ◽  
Author(s):  
Elżbieta Jurkiewicz ◽  
Beata Marcinska ◽  
Katarzyna Malczyk ◽  
Wiesława Grajkowska ◽  
Paweł Daszkiewicz ◽  
...  
Keyword(s):  
Case Report ◽  
Cavernous Malformation ◽  
Review Of The Literature

scholarly journals Giant Cystic Cerebral Cavernous Malformation with Multiple Calcification - Case Report

2013 ◽  
Vol 15 (3) ◽  
pp. 255 ◽  
Author(s):  
Il-Chun Kim ◽  
Ki-Young Kwon ◽  
Jong-Joo Rhee ◽  
Jong-Won Lee ◽  
Jin-Woo Hur ◽  
...  
Keyword(s):  
Case Report ◽  
Cavernous Malformation ◽  
Cerebral Cavernous Malformation

scholarly journals Cavernous Malformation of the Hypoglossal Nerve: Case Report and Review of the Literature

2002 ◽  
Vol 29 (2) ◽  
pp. 191-194 ◽  
Author(s):  
Michael Chow ◽  
Bassam Addas ◽  
Virgilio Sangalang ◽  
Renn Holness
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Facial Nerve ◽  
Nerve Palsy ◽  
Hypoglossal Nerve ◽  
Cavernous Malformation ◽  
Cranial Nerves ◽  
Rare Occurrence ◽  
Review Of The Literature ◽  
Cavernous Malformations

Abstract:Objective:To describe a patient who presented with a hypoglossal nerve palsy caused by a cavernous malformation, review the literature on cavernous malformations associated with cranial nerves and the differential diagnosis of hypoglossal palsy.Results:Partial resection of the lesion was achieved and the diagnosis of cavernous malformation proven histologically.Conclusions:Involvement of a cranial nerve by a cavernous malformation is very uncommon and the facial nerve is the example most frequently reported. This case report adds another possible site for this rare occurrence.

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