Prognostic Factors in Dedifferentiated Chondrosarcoma: A Retrospective Analysis of a Large Series Treated at a Single Institution. [PDF]
, 2019 Background:Dedifferentiated chondrosarcomas (DDCSs) are highly malignant tumors with a dismal prognosis and present a significant challenge in clinical management.
Chebib, Ivan +10 more
core +1 more source
Hereditary multiple exostoses: A case report and literature review
SAGE Open Medical Case Reports, 2022 Osteochondroma is the most common bone tumor representing 20%–50% of all benign bone tumors and 10%–15% of all bone tumors. Osteochondroma has similar radiological appearance in both solitary and multiple forms; the latter is an autosomal dominant ...
Thi Hien Ha +6 more
doaj +1 more source
High-resolution mapping of cancer cell networks using co-functional interactions. [PDF]
, 2018 Powerful new technologies for perturbing genetic elements have recently expanded the study of genetic interactions in model systems ranging from yeast to human cell lines.
Boyle, Evan A +2 more
core +1 more source
Biology of bone sarcomas and new therapeutic developments [PDF]
, 2017 Bone sarcomas are tumours belonging to the family of mesenchymal tumours and constitute a highly heterogeneous tumour group. The three main bone sarcomas are osteosarcoma, Ewing sarcoma and chondrosarcoma each subdivided in diverse histological entities.
Brown, H.K. +4 more
core +1 more source
Osteochondroma of the scapula associated with a subclavian artery pseudoaneurysm: Case report
SAGE Open Medical Case Reports, 2019 Osteochondromas rarely induce vascular complications by mechanical compression. We present the case of a subclavian artery pseudoaneursym caused by an osteochondroma of the scapula in a 67-year-old male.
Ana Oljaca +7 more
doaj +1 more source
, 2014 Background: Complications of solitary or multiple osteochondromas are rare but have been reported in recent literature. Most reported complications arose in patients with multiple and/or sizable osteochondromas.
Bachhuber, D. (Dagmar) +6 more
core +1 more source
Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family [PDF]
, 2010 Background Osteopoikilosis is a rare autosomal dominant genetic disorder, characterised by the occurrence of the hyperostotic spots preferentially localized in the epiphyses and metaphyses of the long bones, and in the carpal and tarsal bones 1 ...
Sevjidmaa Baasanjav +7 more
core +1 more source
A child having rare Hereditary Multiple Exostosis with Covid-19 disease: A case study [PDF]
, 2022 : Hereditary Multiple Exostosis is a rare bone disease in pediatric age group. It is an autosomal dominant disorder, characterized by excessive bony overgrowth arising from lateral aspect of metaphysis of long bone, covered by a cartilaginous cap.
Hasnat, F +3 more
core +2 more sources
Hip Joint Osteochondroma: Systematic Review of the Literature and Report of Three Further Cases
Advances in Orthopedics, 2014 The aim of this study is to systematically review the literature with regards to surgical treatment of patients with hip joint osteochondromas, and to report our surgical management of three paediatric patients who had femoral neck or acetabular ...
Asim M. Makhdom +5 more
doaj +1 more source
Hereditary Multiple Exostoses with Ulnar Hemimelia
Proceedings, 2021 Hereditary Multiple Exostoses is a skeletal dysplasia that is very rare and defined by formation of numerous cartilage capped benign tumours either pedunculated or sessile known as osteochondromas throughout skeleton especially around the growth plates ...
Syed Wasif Ali Shah +5 more
doaj +1 more source