scholarly journals Percutaneous Treatments of Benign Bone Tumors

2018 ◽  
Vol 35 (04) ◽  
pp. 324-332 ◽  
Author(s):  
Roberto Cazzato ◽  
Andrew Gilkison ◽  
Jean Caudrelier ◽  
Julien Garnon ◽  
Afshin Gangi ◽  
...  

AbstractBenign bone tumors consist of a wide variety of neoplasms that do not metastasize but can still cause local complications. Historical management of these tumors has included surgical treatment for lesion resection and possible mechanical stabilization. Initial percutaneous ablation techniques were described for osteoid osteoma management. The successful experience from these resulted in further percutaneous image-guided techniques being attempted, and in other benign bone tumor types. In this article, we present the most common benign bone tumors and describe the available results for the percutaneous treatment of these lesions.

1993 ◽  
Vol 42 (1) ◽  
pp. 409-410
Author(s):  
Takeshi Minamizaki ◽  
Makoto Okuno ◽  
Mitsuru Nakagawa ◽  
Kichizo Yamamoto

2010 ◽  
Vol 134 (10) ◽  
pp. 1460-1466 ◽  
Author(s):  
David R. Lucas

Abstract Osteoblastoma is a rare benign bone tumor. Although the histologic features in most cases are distinctive, there are various permutations that make the diagnosis challenging. It can mimic a variety of other benign bone tumors, but more importantly, distinguishing it from osteoblastoma-like osteosarcoma can be difficult. In this case report, I describe the clinicopathologic findings for a 13-year-old adolescent boy with T7 spinal osteoblastoma and review salient clinical, radiographic, and pathologic features of osteoblastoma, as well as the differential diagnoses.


2017 ◽  
Vol 2017 ◽  
pp. 1-3
Author(s):  
S. E. Roberts ◽  
M. N. Mirzabeigi ◽  
A. Naik ◽  
C. Preciado ◽  
B. Chang

Osteoid osteoma is a benign bone tumor, which represents approximately 10% of all benign bone tumors. When localized to the carpus, osteoid osteomas are most often seen in the scaphoid and capitate. Rarely, these tumors can also be observed in the trapezium. Given the infrequency with which osteomas are located in the trapezium and often nonspecific presenting symptoms, diagnosis of this tumor can be challenging and requires a high index of suspicion.


1992 ◽  
Vol 41 (2) ◽  
pp. 536-539
Author(s):  
Makoto Okuno ◽  
Takeshi Minamizaki ◽  
Atsushi Yamamoto ◽  
Kichizo Yamamoto

2011 ◽  
Vol 14 (3) ◽  
pp. 118-123 ◽  
Author(s):  
Brian T. Welch ◽  
Timothy J. Welch

2021 ◽  
Vol 27 (4) ◽  
pp. 441-445
Author(s):  
P. Lascombes ◽  
◽  
L. Mainard-Simard ◽  
◽  

Introduction The chondromas are a cartilaginous proliferation of mature appearance and moderate size, reason why these tumors are regarded more like hamartomas than real benign tumor. Chondromas represent 10 to 12 % of benign bone tumors. Any bone of an enchondral ossification may be involved. Several bones can be involved, and the disease is called “chondromatosis”. In the review we describe clinical and radiological findings of this pathology as well as indications for reconstructive surgery. Material and methods The review is dedicated to isolated chondromas, periosteal and extraskeletal chondromas, chondromatosis. Results The aspects of epidemiology, clinical presentation, radiology, MRI, prognosis, indications and methods of surgical treatment have been described in the article for each types of chondroma and enchondromatosis. Conclusion Chondromas are benign bone tumors which may be responsible of pathologic fractures. Their surgical treatment consists in curettage and bone grafting or bone-cement filling with or without osteosynthesis. Multiple enchondromatosis should be considered as an osteochondrodysplasia. Its treatment is not the treatment of the multiple chondromas themselves, but of the bone deformities and length discrepancy induced by the disorder. The transformation of some tumors in chondrosarcomas in adolescence or adulthood needs a strict follow up of these patients.


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