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Mountain House, CA, United States

Ross L.,Cedars Sinai Medical Center | Drazin D.,Cedars Sinai Medical Center | Eboli P.,Cedars Sinai Medical Center | Lekovic G.P.,Cedars Sinai Medical Center | Lekovic G.P.,House Clinic House Research Institute
Neurosurgical Focus | Year: 2013

Object. The authors present a series of 4 patients with rare facial nerve tumors. The relevant literature is reviewed and is discussed regarding diagnostic features, the role of operative management, and surgical approach. Methods. A retrospective chart review was conducted for patients with tumors of the facial nerve that were treated between 2008 and 2011. Patients undergoing observationwith serial MRI and thosewho were treated with up-front radiosurgeryand for whom tissue diagnosis was not available were excluded. In addition, patients with suspected vestibular schwannoma, facial nerve schwannoma, neurofibromatosis Type 2, and metastatic disease were also excluded. The charts of 4 patients (2 men and 2 women) with "atypical" tumors were reviewed and analyzed. Results. A total of 12 patients with tumors of the facial nerve were identified during the study period. Patient characteristics, preoperative imaging, operative approach,tumor histology,and outcomes are described. Conclusions. Atypical facial nerve tumors must be distinguished from the more common facial nerve schwannoma.How the authors of this study treat rare facial nerve tumors is basedon their experience with the more common facial nerve schwannomas, characterized by a slow progression of symptoms and growth. Less is known about the rare lesions, and thus a conservativeapproach may be warranted. Open questions include the role of radiosurgery, facial nervedecompression, and indications for resection of tumor and cable grafting for these rare lesions. © Aans, 2013. Source

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