scholarly journals Chondrosarcoma Arising from Benign Bone Tumor due to Malignant Transformation

2011 ◽  
Vol 17 (1) ◽  
pp. 17
Author(s):  
Wan-hyeong Cho ◽  
Won-Seok Song ◽  
Chang-Bae Kong ◽  
Yun-Suk Hong ◽  
Jung-Dong Lee ◽  
...  
Keyword(s):  
Malignant Transformation ◽  
Bone Tumor ◽  
Benign Bone Tumor

False Suggestion of Malignant Transformation of Benign Bone Tumor by 18F-FDG PET/CT

2016 ◽  
Vol 41 (10) ◽  
pp. 774-775 ◽  
Author(s):  
Yu-Ren Chen ◽  
Yu-Cheng Kuo ◽  
Cheng-Nan Hsu ◽  
Te-Chun Hsieh ◽  
Chia-Hung Kao
Keyword(s):  
Malignant Transformation ◽  
Bone Tumor ◽  
Fdg Pet ◽  
Benign Bone Tumor ◽  
Pet Ct ◽  
18F Fdg ◽  
Fdg Pet Ct

scholarly journals Ollier disease: the first report in Syria

2020 ◽  
Vol 2020 (1) ◽  
Author(s):  
Yaseen Dhemesh ◽  
Talha Tawekji ◽  
Mohammad-Nasan Abdul-Baki ◽  
Ghazal Abi-Zamr ◽  
Sawssan Ali
Keyword(s):  
Differential Diagnosis ◽  
Malignant Transformation ◽  
Bone Tumor ◽  
Final Diagnosis ◽  
Benign Bone Tumor ◽  
Pathological Fractures ◽  
Pathological Characteristics ◽  
History Of ◽  
Ollier Disease ◽  
Skeletal Disorder

Abstract Ollier disease is a rare nonhereditary skeletal disorder, characterized by multiple enchondromas, which are noncancerous growth of cartilage. In this report, we present a case of Ollier disease in a 10-year-old Syrian boy. The patient presented with multiple boney masses on hands; he had a history of pathological fractures when he was 5, which caused crippling. We analyzed the clinical, radiographical and pathological characteristics of our patient, which helped us to reach the final diagnosis. Ollier disease is a benign bone tumor, but it has a risk of malignant transformation into chondrosarcoma. The aim of this report is to document the presence of Ollier disease in Syria to help other Syrian physicians considering this disease in the differential diagnosis if they face similar presentations.

scholarly journals Osteochondroma of the Scapula with Accessory Nerve (XI) Compression

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Philippe Beauchamp-Chalifour ◽  
Stéphane Pelet
Keyword(s):  
Malignant Transformation ◽  
Growth Plate ◽  
Bone Tumor ◽  
Nerve Compression ◽  
Accessory Nerve ◽  
Long Bones ◽  
Benign Bone Tumor ◽  
Surgical Indications

Osteochondroma is the most common benign bone tumor and is characterized as a cartilage-capped bony stalk. This lesion usually develops from the growth plate of long bones. Most osteochondromas are asymptomatic. Neurovascular compressions or cosmetic issues can occur in specific locations. Malignant transformation is extremely rare, and MRI can help evaluate these lesions. Symptomatic mass and malignancy features are the main surgical indications. Uncommonly, an osteochondroma can develop from flat bones. We present the case of a 25-year-old patient with a right scapula osteochondroma causing an accessory nerve compression. The mass was surgically removed, and the diagnosis was confirmed. The patient fully recovered at the latest 3-year follow-up visit.

Fusion of the COL1A1 and USP6 genes in a benign bone tumor

2008 ◽  
Vol 180 (1) ◽  
pp. 70-73 ◽  
Author(s):  
Ioannis Panagopoulos ◽  
Fredrik Mertens ◽  
Richard Löfvenberg ◽  
Nils Mandahl
Keyword(s):  
Bone Tumor ◽  
Benign Bone Tumor

scholarly journals Grafting for bone defects after curettage of benign bone tumor – Analysis of factors influencing the bone healing

2018 ◽  
Vol 81 (7) ◽  
pp. 643-648 ◽  
Author(s):  
Po-Kuei Wu ◽  
Cheng-Fong Chen ◽  
Chao-Ming Chen ◽  
Shang-Wen Tsai ◽  
Yu-Chi Cheng ◽  
...  
Keyword(s):  
Bone Healing ◽  
Bone Tumor ◽  
Bone Defects ◽  
Benign Bone Tumor ◽  
Factors Influencing

Giant ossifying fibroma of the skull

1983 ◽  
Vol 58 (4) ◽  
pp. 602-606 ◽  
Author(s):  
Jean-Guy Villemure ◽  
Kathleen Meagher-Villemure
Keyword(s):  
Surgical Management ◽  
Bone Tumor ◽  
Parietal Bone ◽  
Cranial Vault ◽  
Ossifying Fibroma ◽  
Benign Bone Tumor ◽  
Content Type ◽  
Extensive Growth ◽  
Fine Print

✓ A case of giant ossifying fibroma of the cranial vault is reported. The rapid extensive growth of this large parietal bone tumor inaccurately suggested malignancy. The literature relative to this benign bone tumor as well as its surgical management and follow-up findings are presented.

Osteochondroma of the Talar Neck

2005 ◽  
Vol 95 (3) ◽  
pp. 295-297 ◽  
Author(s):  
Selçuk Keser ◽  
Ahmet Bayar
Keyword(s):  
Bone Tumor ◽  
Benign Bone Tumor ◽  
Anterior Portion ◽  
Solitary Osteochondroma

Osteochondroma is the most common benign bone tumor. It rarely affects rearfoot bones, and only a few cases of talar osteochondroma have been reported. We report a case of a solitary osteochondroma of the talus that presented as a painful callus on the anterior portion of the ankle that was refractory to dermatologic treatment. (J Am Podiatr Med Assoc 95(3): 295–297, 2005)

scholarly journals Osteochondroma of the Mandibular Condyle

2012 ◽  
Vol 2 (3) ◽  
pp. 106-108 ◽  
Author(s):  
Jyotsna Galinde ◽  
Sushrut Vaidya ◽  
Sunil Sidana ◽  
Srivalli Natrajan
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Bone Tumor ◽  
Mandibular Condyle ◽  
Neck Region ◽  
Rare Tumor ◽  
Benign Bone Tumor ◽  
Head And Neck Region ◽  
Condylar Process ◽  
Condylar Hyperplasia

ABSTRACT Osteochondroma is the most common benign bone tumor but rare in the head and neck region because of intramembranous origin of craniofacial bones. In the head and neck it occurs most commonly at tip of coronoid or condylar process. Clinically features can mimic condylar hyperplasia. This case report adds to the growing knowledge about this rare tumor. How to cite this article Vaidya S, Sidana S, Galinde J, Natrajan S. Osteochondroma of the Mandibular Condyle. J Contemp Dent 2012;2(3):106-108.

Osteoblastoma

2010 ◽  
Vol 134 (10) ◽  
pp. 1460-1466 ◽  
Author(s):  
David R. Lucas
Keyword(s):  
Case Report ◽  
Bone Tumor ◽  
Bone Tumors ◽  
Differential Diagnoses ◽  
Benign Bone Tumor ◽  
Benign Bone Tumors ◽  
Pathologic Features ◽  
Clinicopathologic Findings

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.

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