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Extraskeletal Osteosarcoma of the Hand in an AdolescentA Case Report
Davi Gabriel Bellan, MD1; Reynaldo Jesus-Garcia, MD, PhD1; Maria Teresa de Seixas Alves, MD, PhD2; Marcelo de Toledo Petrilli, MD1; Antonio Sérgio Petrilli, MD, PhD3; Marcos Korukian, MD1; Dan Carai Maia Viola, MD1; Murillo Ferri Schoedl, MD1; Andreza Almeida Senerchia, MD3
1 Department of Ortopedia, Universidade Federal de São Paulo, Rua Napoleão de Barros, 715 CEP 04038-032, São Paulo/SP, Brazil. E-mail address for D.G. Bellan: dgbellan@gmail.com
2 Department of Patologia, Universidade Federal de São Paulo, Rua Botucatu, 740 CEP 04023-900, São Paulo/SP, Brazil
3 IOP/GRAACC – Department of Pediatria, Universidade Federal de São Paulo, Rua Botucatu, 743 CEP 04023-062, São Paulo/SP, Brazil
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  • Disclosure statement for author(s): PDF

Investigation performed at the Institute of Pediatric Oncology, Universidade Federal de São Paulo, São Paulo, Brazil



Disclosure: None of the authors received payments or services, either directly or indirectly (i.e., via his or her institution), from a third party in support of any aspect of this work. None of the authors, or their institution(s), have had any financial relationship, in the thirty-six months prior to submission of this work, with any entity in the biomedical arena that could be perceived to influence or have the potential to influence what is written in this work. Also, no author has had any other relationships, or has engaged in any other activities, that could be perceived to influence or have the potential to influence what is written in this work. The complete Disclosures of Potential Conflicts of Interest submitted by authors are always provided with the online version of the article.

Copyright © 2013 by The Journal of Bone and Joint Surgery, Inc.
JBJS Case Connector, 2013 Jan 23;3(1):e6 1-5. doi: 10.2106/JBJS.CC.L.00004
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Extract

Extraskeletal osteosarcoma (ESOS) is a well-defined and rare soft-tissue neoplasm characterized by osteoid production with no association with bone1. It represents 1% of all soft-tissue sarcomas and 4% to 5% of all osteosarcomas1-3.
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