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Related to osteoblastoma: osteochondroma, enchondroma, chondroblastoma
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We report the case of a 49-year-old man with a petrous apex osteoblastoma that presumably underwent malignant transformation into an osteosarcoma with subsequent distant metastasis.
Age 0-20 years 20-50 years >50 year Osteoblastoma Non-Hodgkin's Paget's Disease Lymphoma * Osteoid Osteoma * Osteosarcoma Lymphoma Fibrous dysplasia Giant Cell Tumor * metastatic carcinoma Hodgkins Lymphoma Aneurysmal Bone Cyst Multiple Myeloma Osteochondroma * Chondroblastoma Chondrosarcoma Ewing sarcoma Spindle cell sarcoma (eg Fibrosarcoma) * Osteosarcoma Osteomyelitis Aneurysmal Bone Cyst Chondroblastoma
Benign bone-forming lesions: osteoma, osteoid osteoma, and osteoblastoma - clinical, imaging, pathologic, and differential consideration.
We encountered a patient with benign osteoblastoma of the pubic ramus of right side.
Radiografide ayrici tanilarda stres kirigi, enfeksiyon, osteoblastoma, eosinofilik granulom ve cok nadir de olsa osteosarkom goz onunde bulundurulmalidir (2).
Clinicopathologic features and treatment of osteoid osteoma and osteoblastoma in children and adolescents.
6) We present a rare case of a large sacral osteoblastoma in a pediatric patient that was treated with a multidisciplinary team involving the departments of neurosurgery, neuroendovascular surgery, colorectal surgery, urological surgery, and various rehabilitation teams.
C-Fos (FOS; FBJ murine osteoblastoma viral oncogene homoIog)-induced growth factor, a member of tkcAP-l oncogene family implicated in cell motility and invasion (Han et al.
To study cell proliferation, differentiation, and cell adhesion, scaffolds were seeded with MG63 (human osteoblastoma cell line; ATCC, Manassas, VA) cells.
Other new information relates to chondroblastoma, osteoblastoma, and parosteal osteosarcoma, and the section on neoplasm simulators has been expanded to include conditions like neuropathic joint that may present as a neoplasm.
Benign osteoblastoma was independently described for the first time by Jaffe and Lichfenstein in 1956 as a vascular, osteoid and bone-forming tumour cytologically characterized by osteoblasts (1-2).
Los QOA secundarios se relacionan a neoplasias secundarias mas frecuentemente TCG, osteoblastoma, condroblastoma u osteosarcoma que causan obstruccion venosa o fistula arteriovenosa (5).
Benign lesions that must be distinguished from malignant tumors include osteoid osteoma, hemangioma, osteoblastoma, giant cell tumor and aneurysmal bone cysts.
Osteoblastoma may occur in the vertebral pedicle, most often in children aged 10-15 years.
There are two forms of ABC- Primary (Occurring de novo) and secondary which complicates other benign and malignant conditions like-Fibrous Dysphasia, Osteoblastoma, Osteosarcoma, Chondroblastoma, Giant Cell tumour, chondromyxoid fibroma, non-ossifying fibroma.