| Literature DB >> 24656765 |
Mohammed Tahir Ansari1, Shishir Rastogi2, Shah Alam Khan3, Chandershekhar Yadav3, Laxman Rijal4.
Abstract
Schwannomas of osseous origin are rare, and schwannomas of the short tubular bones are even rarer. These benign-looking tumors are difficult to diagnose using imaging alone. However, histopathologic evaluation of a biopsy specimen can establish the diagnosis by identifying Antoni type A and B zones. Curettage and bone grafting will probably be adequate for treatment because malignant changes are unlikely. Large lesions can require en bloc excision and reconstruction. We describe what appears to be only the second case of a schwannoma in the first metatarsal of the foot in a 48-year-old woman. The lesion was poorly contained, with obvious breaks in the cortical shell. The diagnosis was confirmed by pathologic analysis. The lesion was successfully treated with en bloc resection and reconstruction with a nonvascularized fibular graft.Entities:
Keywords: Schwann cell; bone; fibula; nerve sheath; neurilemmoma; tumor
Mesh:
Year: 2014 PMID: 24656765 DOI: 10.1053/j.jfas.2014.01.014
Source DB: PubMed Journal: J Foot Ankle Surg ISSN: 1067-2516 Impact factor: 1.286