Bilateral bifid labyrinthine facial nerve anomalies associated with agenesis of the oval window: Case report and review of the literature

2011 ◽  
Vol 121 (S4) ◽  
pp. S195-S195
Author(s):  
Andrew K. Patel ◽  
Thomas H. Alexander ◽  
Roberto A. Cueva
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
Oval Window ◽  
Review Of The Literature

scholarly journals Congenital unilateral facial palsy revealing a facial nerve agenesis: a case report and review of the literature

2019 ◽  
Vol 5 (1) ◽  
pp. 20180029
Author(s):  
Yaotse Elikplim Nordjoe ◽  
Ouidad Azdad ◽  
Mohamed Lahkim ◽  
Laila Jroundi ◽  
Fatima Zahrae Laamrani
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
Temporal Bone ◽  
Facial Paralysis ◽  
Facial Palsy ◽  
Rare Condition ◽  
Review Of The Literature ◽  
Moebius Syndrome ◽  
Temporal Bone Ct

Facial nerve aplasia is an extremely rare condition that is usually syndromic, namely, in Moebius syndrome. The occurrence of isolated agenesis of facial nerve is even rarer, with only few cases reported in the literature. We report a case of congenital facial paralysis due to facial nerve aplasia diagnosed on MRI, while no noticeable abnormality was detected on the temporal bone CT.

A Synchronous Facial Nerve Schwannoma and Neurofibroma: Case Report and Review of the Literature

2011 ◽  
Vol 121 (S4) ◽  
pp. S119-S119
Author(s):  
BC Gross ◽  
ML Carlson ◽  
B Scheithauer ◽  
CLW Driscoll ◽  
EJ Moore
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
Review Of The Literature ◽  
Facial Nerve Schwannoma

Large intraparotid facial nerve schwannoma: Case report and Review of the Literature

2008 ◽  
Vol 37 (7) ◽  
pp. 679-681 ◽  
Author(s):  
N.S. Salemis ◽  
A. Karameris ◽  
S. Gourgiotis ◽  
P. Stavrinou ◽  
K. Nazos ◽  
...  
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
Review Of The Literature ◽  
Facial Nerve Schwannoma

Multiple Familial Facial Glomus: Case Report and Review of the Literature

2003 ◽  
Vol 112 (3) ◽  
pp. 287-292 ◽  
Author(s):  
Giuseppe Magliulo ◽  
Erika Parnasi ◽  
Raffaello D'Amico ◽  
Vincenzo Savastano ◽  
Salvatore Romeo
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
English Language ◽  
Facial Canal ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
First Report ◽  
English Language Literature ◽  
Language Literature

Facial paraganglioma is an extremely rare tumor that originates from abnormal paraganglionic tissue situated in the intrapetrous facial canal. A review of the English-language literature shows that only 8 cases of facial nerve paraganglioma have been published. In each case the facial glomus presented itself sporadically, completely independent of any other form of paraganglioma. This study reports an intrapetrous facial glomus that occurred in a case of multiple paragangliomas with a hereditary pattern. To our knowledge, this is the first report of such a combination.

scholarly journals Bilateral Facial Nerve Schwannoma: A Case Report and Review of the Literature

2021 ◽  
Vol 13 (2) ◽  
pp. 47-52
Author(s):  
Kayvan Aghazadeh ◽  
Benyamin Rahmaty ◽  
Ali Kouhi ◽  
Sasan Dabiri ◽  
Saeed Sohrabpour ◽  
...  
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
Review Of The Literature ◽  
Facial Nerve Schwannoma

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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