Results 41 to 50 of about 13,213 (233)

Infrapatellar Fat Pad Para-Articular Osteochondroma: A Ten-Year Follow-up and Review [PDF]

, 2015
Introduction: Para-articular masses are not clear enough in terms of their etiology and nomenclature. Although surgical removal of the mass is the preferred treatment, long term follow-up after surgical treatment has not been reported yet.
Bilgin, E., Bombaci, H.
core   +1 more source

Solitary Osteochondroma in Uncommon Sites- A Rare Case Report

Journal of Orthopaedic Case Reports
Introduction: Osteochondroma is a bony lesion arising from the surface of the bone. It com-prises a large percentage of all benign bone tumors. A unique feature of this tumor is the conti-nuity of cortical and medullary components between the normal bony
Karthik Loganathan, Prabhu Vasudevan, Ajithkumar Krishnan, Nawinsurya Arunachalam, Akash Manivannan   +4 more
doaj   +1 more source

Osteochondroma: Review of 431 patients from one medical institution in South China

Journal of Bone Oncology, 2017
Background The geographic distribution of osteochondroma (OC) varies greatly around the world. There has been no recent report on OC in a large Chinese population.
K. Tong, Hongzhe Liu, Xiangui Wang, Ziyi Zhong, Shenglu Cao, C. Zhong, Yunping Yang, G. Wang   +7 more
semanticscholar   +1 more source

Solitary osteochondroma of the twelfth rib with intraspinal extension and cord compression in a middle-aged patient

BMC Musculoskeletal Disorders, 2012
Background Osteochondroma is a disease of growing bone and thus typically presents in younger patients. It has rarely been described in middle-aged and elderly patients.
Shim Jung, Park Choon, Shin Seung, Jeong Hee, Hwang Jang   +4 more
doaj   +1 more source

Solitary Osteochondroma of the Spine—A Case Series: Review of Solitary Osteochondroma With Myelopathic Symptoms

Global Spine Journal, 2017
Study Design: Case series and literature review. Objective: There is a growing body of literature supporting that osteochondroma of the spine may not be as rare as previously documented.
Ramakanth R. Yakkanti, I. Onyekwelu, L. Carreon, J. Dimar   +3 more
semanticscholar   +1 more source

A Solitary Osteochondroma Originating from the Spinous Process of the Third Cervical Vertebra: A Case Report and Comprehensive Literature Review

Journal of Spine Practice
Background Osteochondroma is one of the most common solitary bone lesions. Multiple lesions are possible only in some genetic abnormalities, such as hereditary multiple exostoses (HME).
Jinan Mohammed Aljasem, Abdulaziz Yousef Alahmed, Osama Abdullah Barnawi, Ghaida Ali Aljdhaa, Abdullah Salem Almalki, Ahmed Bin Ali Albinali, Ali Hussain Dallak, Jehad Mahmoud Ahmed, Abdullah Qaddah Alqahtani   +8 more
doaj   +1 more source

Osteochondroma involving mandibular condyle

Journal of Indian Academy of Oral Medicine and Radiology, 2017
Osteochondroma is defined as an osteocartilagenous exostosis with cartilage capped exophytic lesion that arises from the bone cortex. It is a slow growing benign tumor that is rarely seen in the maxillofacial region.
Latika Bachani, Ashok Lingappa, Shivaprasad Shankaramurthy, Sujatha Gulagadar Parameshwarappa   +3 more
doaj   +1 more source

Unsuspected osteochondroma-like outgrowths in the cranial base of Hereditary Multiple Exostoses patients and modeling and treatment with a BMP antagonist in mice

PLoS Genetics, 2017
Hereditary Multiple Exostoses (HME) is a rare pediatric disorder caused by loss-of-function mutations in the genes encoding the heparan sulfate (HS)-synthesizing enzymes EXT1 or EXT2.
Sayantani Sinha, Christina Mundy, Till E Bechtold, F. Sgariglia, M. Ibrahim, P. Billings, K. Carroll, E. Koyama, Kevin B. Jones, M. Pacifici   +9 more
semanticscholar   +1 more source

Management of a Case of Ruptured Pseudoaneurysm and Stenosis of Femoral Artery Caused by Femoral Osteochondroma [PDF]

Journal of Clinical and Diagnostic Research, 2015
We present a rare case of ruptured pseudoaneurysm of distal femoral artery due to osteochondroma in a 21-year- old male. The patient was initially treated for osteochondroma as ruptured pseudoaneurysm was not suspected.
Vikas Deep Goyal, Vipin Sharma, Sandeep Kalia, Shivam Pathak   +3 more
doaj   +1 more source

Acral Mesenchymal Spindle Cell Neoplasm With a Novel HMGA2::NCOA2 Fusion

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Molecular profiling has revolutionized the field of soft tissue pathology, enhancing diagnostic precision and treatment strategies. The integration of molecular analysis and immunohistochemistry has been crucial for classifying diagnostically challenging acral mesenchymal neoplasms.
Grace Z. Armstrong, Carina A. Dehner, Eitan Halper‐Stromberg, Esther Baranov, Anna C. Eden, Rachel P. Kowal   +5 more
wiley   +1 more source