Bone Sarcomas and Desmoids - 16/11/19
Doi : 10.1016/j.hoc.2019.09.002
Jeremy M. Brownstein, MD a, b, Thomas F. DeLaney, MD c, ⁎ 
a Francis H. Burr Proton Beam Therapy Center, Massachusetts General Hospital, 30 Fruit Street, Boston, MA 02114, USA
b Department of Radiation Oncology, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA
c Department of Radiation Oncology, Harvard Medical School, Francis H. Burr Proton Therapy Center, Massachusetts General Hospital, 30 Fruit Street, Boston, MA 02114, USA
∗Corresponding author.
Résumé |
Bone sarcomas are rare tumors arising in bone, representing only a small fraction of solid malignant tumors. Desmoids are benign, infiltrative soft tissue neoplasms. Because of their scarcity and a paucity of data, the management of these tumors can be challenging, especially for clinicians who infrequently encounter these tumors. This article reviews the current literature regarding the diagnosis, work-up, and treatment of these uncommon mesenchymal tumors.
Le texte complet de cet article est disponible en PDF.Keywords : Osteosarcoma, Chondrosarcoma, Chordoma, Desmoid, Radiation therapy
Plan
| Disclosure: The authors have nothing to disclose. |
© 2019
Elsevier Inc. Tous droits réservés.
Vol 34 - N° 1
P. 177-188 - février 2020 Retour au numéro
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