Hereditary multiple exostoses (HME), also called hereditary multiple osteochondromas, is a
rare genetic disorder characterized by multiple osteochondromas that grow near the growth …

Hereditary multiple exostoses (HME) is an inherited genetic condition characterized by the
presence of multiple exostoses (osteochondromas). MHE is a relatively rare autosomal …

Ollier disease (OD) and Maffucci syndrome (MS) are characterized by multiple
enchondromas. Patients with MS also have benign vascular overgrowths that become …

Objective To analyze the results of annual screening using whole-body magnetic resonance
imaging (WBMRI) in patients with multiple hereditary exostoses (MHE) and …

Objective: Classical chondrosarcoma has poor sensitivity to chemotherapy and
radiotherapy, and surgical resection is the only effective treatment. Therefore, development …

Abstract Osteochondromas account for 20%–50% of all benign bone lesions. These tumors
may present as solitary non-hereditary lesions, which are the most common presentation, or …

Chondrosarcomas in children and adolescents are uncommon and constitute< 5% of all
chondrosarcomas. There are very few studies discussing extremity chondrosarcomas in …

Background Hereditary multiple exostoses (HME) is a rare skeletal disorder characterised
by a widespread. distribution of osteochondromas originating from the metaphyses of long …

Purpose To evaluate the results of total-body (TB) MRI used as a screening tool for
assessment or exclusion of malignant transformation in patients with hereditary multiple …

Solitary osteochondromas are common, benign hyaline cartilage-capped exostoses that
primarily arise from the metaphyses of long and flat bones. Diaphyseal aclasis is an …