A Case of Schwannoma Arising in Pterygopalatine Fossa.
- Author:
Seog Kyun MUN
1
;
Hang Sun CHO
;
Youn Kyoung DO
;
Young Ho HONG
Author Information
1. Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, Chung-Ang University, Seoul, Korea. entdoctor@cau.ac.kr
- Publication Type:Case Report
- Keywords:
Schwannoma;
Pterygopalatine fossa
- MeSH:
Angiofibroma;
Diagnosis, Differential;
Head;
Histiocytoma, Malignant Fibrous;
Lymphoma;
Melanoma;
Neck;
Neurilemmoma;
Pterygopalatine Fossa;
Rhabdomyosarcoma;
Schwann Cells
- From:Korean Journal of Otolaryngology - Head and Neck Surgery
2008;51(6):552-555
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Schwannoma, also referred to as neurilemmoma, is an encapsulated benign soft tissue tumor arising from the schwann cells of the nerve sheath. Although 25 to 45% of schwannomas arise in the head and neck region, pterygopalatine fossa is the rarest sites of involvement with only 23 cases reported in the medical literature. It is usually seen in the second and fifth decades, but sex or racial predilection has not been noted. Clinical features of this tumor are dependent on the involved anatomical site, nerve of origin, and compression of adjacent structures. The differential diagnosis of masses in pterygopalatine fossa includes angiofibroma, fibrous histiocytoma, malignant melanoma, lymphoma, and low-grade rhabdomyosarcoma. The treatment of choice is that the tumor is completely removed with careful preservation of its nerve. Recently, the authors experienced a case of schwannoma arising in pterygopalatine fossa, which was removed with transantral approach. Hence, we report a rare case with a review of literature.
