Abstract
Definition: Benign cartilaginous tumor of childhood, usually epiphyseal.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Selected Bibliography
Amary MF, Berisha F, Mozela R, Gibbons R, Guttridge A, O’Donnell P, Baumhoer D, Tirabosco R, Flanagan AM. The H3F3 K36M mutant antibody is a sensitive and specific marker for the diagnosis of chondroblastoma. Histopathology. 2016;69(1):121–7.
Bacchini P, Inwards C, Biscaglia R, Picci P, Bertoni F. Chondroblastoma-like osteosarcoma. Orthopedics. 1999;22(3):337–9.
Kaim AH, Hügli R, Bonél HM, Jundt G. Chondroblastoma and clear cell chondrosarcoma: radiological and MRI characteristics with histopathological correlation. Skeletal Radiol. 2002;31(2):88–95.
Lin PP, Thenappan A, Deavers MT, Lewis VO, Yasko AW. Treatment and prognosis of chondroblastoma. Clin Orthop Relat Res. 2005;(438):103–9.
Sailhan F, Chotel F, Parot R, SOFOP. Chondroblastoma of bone in a pediatric population. J Bone Joint Surg Am. 2009;91(9):2159–68.
Springfield DS, Capanna R, Gherlinzoni F, Picci P, Campanacci M. Chondroblastoma. A review of seventy cases. J Bone Joint Surg Am. 1985;67(5):748–55.
Xie C, Jeys L, James SL. Radiofrequency ablation of chondroblastoma: long-term clinical and imaging outcomes. Eur Radiol. 2015;25(4):1127–34.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Staals, E.L. (2020). Chondroblastoma. In: Picci, P., et al. Diagnosis of Musculoskeletal Tumors and Tumor-like Conditions. Springer, Cham. https://doi.org/10.1007/978-3-030-29676-6_17
Download citation
DOI: https://doi.org/10.1007/978-3-030-29676-6_17
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-29675-9
Online ISBN: 978-3-030-29676-6
eBook Packages: MedicineMedicine (R0)