| Literature DB >> 20637426 |
Pedro Paulo de Andrade Santos1, Valéria Souza Freitas, Leão Pereira Pinto, Roseana de Almeida Freitas, Lélia Batista de Souza.
Abstract
Schwannomas, also known as neurilemmomas, are uncommon neoplasms apparently derived from Schwann cells. The growth of these tumors causes displacement and compression of the nerve of origin. Schwannomas are usually solitary lesions but can be multiple when associated with neurofibromatosis. Anti-S100 protein is the most widely used antibody for the identification of this neoplasm. Surgical excision is the treatment of choice for schwannomas, with few and controversial reports of recurrence or malignant transformation. The present article reports 7 additional cases of oral schwannoma, and the literature is reviewed regarding clinicopathologic features, immunohistochemical findings, differential diagnosis, and therapeutic management of this benign neural tumor. Crown Copyright 2010. Published by Elsevier Inc. All rights reserved.Entities:
Mesh:
Year: 2010 PMID: 20637426 DOI: 10.1016/j.anndiagpath.2010.02.009
Source DB: PubMed Journal: Ann Diagn Pathol ISSN: 1092-9134 Impact factor: 2.090