TY - JOUR
T1 - Intracanalicular schwannoma of the facial nerve
T2 - A manifestation of neurofibromatosis type 2
AU - Saada, Ahmed A.
AU - Limb, Charles J.
AU - Long, Donlin M.
AU - Niparko, John K.
PY - 2000/4
Y1 - 2000/4
N2 - Primary facial nerve tumors, which are relatively uncommon, can present a diagnostic dilemma based on their location and variable pattern of symptoms. Of primary cranial nerve tumors, schwannomas of the facial nerve rank third in frequency after those of the eighth and fifth cranial nerves. We report an illustrative case of an intracanalicular schwannoma associated with several central nervous system tumors, consistent with neurofibromatosis type 2. Initially assumed to be an eighth cranial nerve tumor, the schwannoma was found intraoperatively to arise from the facial nerve. Early diagnosis and treatment enabled excision of the tumor without sacrifice of the facial nerve. Facial nerve schwannomas can resemble acoustic schwannomas in their clinical presentation. Only a heightened level of clinical vigilance will point to the correspond diagnosis and result in an optimal therapeutic outcome for patients with these rare tumors.
AB - Primary facial nerve tumors, which are relatively uncommon, can present a diagnostic dilemma based on their location and variable pattern of symptoms. Of primary cranial nerve tumors, schwannomas of the facial nerve rank third in frequency after those of the eighth and fifth cranial nerves. We report an illustrative case of an intracanalicular schwannoma associated with several central nervous system tumors, consistent with neurofibromatosis type 2. Initially assumed to be an eighth cranial nerve tumor, the schwannoma was found intraoperatively to arise from the facial nerve. Early diagnosis and treatment enabled excision of the tumor without sacrifice of the facial nerve. Facial nerve schwannomas can resemble acoustic schwannomas in their clinical presentation. Only a heightened level of clinical vigilance will point to the correspond diagnosis and result in an optimal therapeutic outcome for patients with these rare tumors.
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U2 - 10.1001/archotol.126.4.547
DO - 10.1001/archotol.126.4.547
M3 - Article
C2 - 10772314
AN - SCOPUS:0034075085
SN - 2168-6181
VL - 126
SP - 547
EP - 549
JO - Archiv fur klinische und experimentelle Ohren- Nasen- und Kehlkopfheilkunde
JF - Archiv fur klinische und experimentelle Ohren- Nasen- und Kehlkopfheilkunde
IS - 4
ER -