Extracorporeally Irradiated Autograft-prosthetic Composite Arthroplasty With Vascular Reconstruction for Primary Bone Tumor of the Proximal Tibia

2011 ◽  
Vol 2011 ◽  
pp. 288-290
Author(s):  
C.P. Beauchamp
2011 ◽  
Vol 25 (2) ◽  
pp. 266.e1-266.e4 ◽  
Author(s):  
Makoto Emori ◽  
Nobuyuki Hashimoto ◽  
Ken-Ichiro Hamada ◽  
Norifumi Naka ◽  
Hiroshi Takami ◽  
...  

Bone Reports ◽  
2020 ◽  
Vol 13 ◽  
pp. 100421
Author(s):  
Valérie Trichet ◽  
Louis-Romée Le Nail ◽  
Régis Brion ◽  
Françoise Rédini ◽  
François Vallette ◽  
...  

2018 ◽  
Vol 40 (7) ◽  
pp. 555-557
Author(s):  
Daniel Koh ◽  
Theodore Lau ◽  
Evonne Teoh ◽  
Kenneth K. Lau

2020 ◽  
Vol 10 ◽  
Author(s):  
Zhong-Wei Luo ◽  
Pan-Pan Liu ◽  
Zhen-Xing Wang ◽  
Chun-Yuan Chen ◽  
Hui Xie

Osteosarcoma is a malignant primary bone tumor commonly occurring in children and adolescents. The treatment of local osteosarcoma is mainly based on surgical resection and chemotherapy, whereas the improvement of overall survival remains stagnant, especially in recurrent or metastatic cases. Tumor microenvironment (TME) is closely related to the occurrence and development of tumors, and macrophages are among the most abundant immune cells in the TME. Due to their vital roles in tumor progression, macrophages have gained increasing attention as the new target of tumor immunotherapy. In this review, we present a brief overview of macrophages in the TME and highlight the clinical significance of macrophages and their roles in the initiation and progression of osteosarcoma. Finally, we summarize the therapeutic approaches targeting macrophage, which represent a promising strategy in osteosarcoma therapies.


2015 ◽  
Vol 15 (6) ◽  
pp. 638-640 ◽  
Author(s):  
Scott A. Wallace ◽  
Romeo C. Ignacio ◽  
Arnett Klugh ◽  
Gregory Gates ◽  
Marion C. W. Henry

Osteoblastoma is an uncommon primary bone tumor that usually presents as a painful lesion in a long bone or in the spine. Osteoblastoma has been reported only twice in the literature in conjunction with systemic fibromatosis. The authors report the case of an 8-year-old girl with suspected Klippel-Trenaunay-Weber syndrome, a rare syndrome of systemic fibromatosis, who presented with a painless thoracic rib lesion that was found to be an osteoblastoma.


Bone ◽  
2008 ◽  
Vol 42 ◽  
pp. S94
Author(s):  
Loic Geffroy ◽  
Damien Chauviere ◽  
Francois Lamoureux ◽  
Gaelle Picarda ◽  
Olivier Delattre ◽  
...  

1996 ◽  
Vol 25 (2) ◽  
pp. 174-177 ◽  
Author(s):  
John L. DeFilippo ◽  
J. S. Yu ◽  
Lawrence Weis ◽  
Joel Lucas

Sign in / Sign up

Export Citation Format

Share Document