Back to Search Start Over

Stereotactic radiosurgery for facial nerve hemangioma: Case report and systematic review.

Authors :
Park, David J.
Hori, Yusuke S.
Nernekli, Kerem
Persad, Amit R.
Tayag, Armine
Ustrzynski, Louisa
Emrich, Sara C.
Hancock, Steven L.
Chang, Steven D.
Source :
Journal of Clinical Neuroscience; Aug2024, Vol. 126, p21-25, 5p
Publication Year :
2024

Abstract

• Facial nerve hemangiomas are rare tumors that can cause facial nerve dysfunction. • The optimal approach for treating FNHs remains uncertain due to their rarity. • This case demonstrates the feasibility of SRS as a standalone treatment. Facial nerve hemangiomas (FNHs) are rare tumors that primarily occur near the geniculate ganglion in the temporal bone. Despite their rarity, they can cause significant facial nerve dysfunction. The optimal management approach for FNHs remains uncertain, with surgery being the mainstay but subject to debate regarding the extent of resection and preservation of the facial nerve. Systematic review was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. We queried the PubMed/Medline (accessed on 5 March 2024) electronic database using combinations of the following search terms and words text: "geniculate ganglion hemangioma", "ganglional hemangioma", "hemangioma of the facial nerve", "facial hemangioma", and "intratemporal hemangioma". We identified a total of 30 literatures (321 patients). The most common site involved for the facial nerve hemangioma was the geniculate ganglion area followed by internal auditory canal, tympanic segment, labyrinthine segment and mastoid involvement. All patients were treated with conservative management or surgery. We report a 48-year-old female patient with HB grade 2 facial palsy and hemifacial spasm underwent SRS using Cyberknife technology. The treatment targeted the FNH in the left internal acoustic canal near the geniculate ganglion. Six months post-treatment, clinical improvement was evident, and lesion control was confirmed in a follow-up brain MRI. The rarity of FNHs contributes to the lack of consensus on optimal management. This illustrative case demonstrates the feasibility of SRS as a standalone treatment for FNHs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09675868
Volume :
126
Database :
Supplemental Index
Journal :
Journal of Clinical Neuroscience
Publication Type :
Academic Journal
Accession number :
178786728
Full Text :
https://doi.org/10.1016/j.jocn.2024.05.023