Hallux Osteoid Osteoma: A Case Report and Literature Review
Konstantinos C. Xarchas*, George Kyriakopoulos, Spyros Manthas, Leon Oikonomou
Identifiers and Pagination:Year: 2017
First Page: 1066
Last Page: 1072
Publisher ID: TOORTHJ-11-1066
Article History:Received Date: 05/06/2017
Revision Received Date: 26/07/2017
Acceptance Date: 12/08/2017
Electronic publication date: 30/09/2017
Collection year: 2017
open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Osteoid osteoma is a benign bone tumour that mostly affects males in the second and third decade of their life. The lesion mainly occurs in long bones, usually in the femur and tibia, causing severe localized pain that is worse at night and responds to nonsteroidal anti-inflammatory drugs (NSAIDs). Diagnosis is usually made on the basis of history and radiographic findings. However, in more unusual locations as the hand and foot, diagnostic issues can arise. Treatment often includes complete removal of the tumor. We present a 22 year old male with osteoid osteoma involving the distal phalanx of the hallux. To our knowledge very few cases of great toe osteoid osteoma have been reported in the literature.