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Imaging of solitary and multiple osteochondromas: From head to toe - A review.
Pontes ÍCM, Leão RV, Lobo CFT, Paula VT, Yamachira VS, Baptista AM, Helito PVP. Pontes ÍCM, et al. Clin Imaging. 2023 Nov;103:109989. doi: 10.1016/j.clinimag.2023.109989. Epub 2023 Sep 26. Clin Imaging. 2023. PMID: 37778187 Review.
These tumors may present as solitary non-hereditary lesions, which are the most common presentation, or as multiple tumors associated with hereditary conditions. Plain radiography is the imaging method of choice and demonstrates the typical cortical and medullary continuit …
These tumors may present as solitary non-hereditary lesions, which are the most common presentation, or as multiple tumors associated …
Insights into the molecular regulatory network of pathomechanisms in osteochondroma.
Yang C, Zhang R, Lin H, Wang H. Yang C, et al. J Cell Biochem. 2019 Oct;120(10):16362-16369. doi: 10.1002/jcb.29155. Epub 2019 Jun 18. J Cell Biochem. 2019. PMID: 31211456 Review.
Osteochondroma is a benign autosomal dominant hereditary disease characterized by abnormal proliferation of cartilage in the long bone. It is divided into solitary osteochondroma and hereditary multiple exostoses (HMEs). ...
Osteochondroma is a benign autosomal dominant hereditary disease characterized by abnormal proliferation of cartilage in the long …
Osteosarcoma and other bone cancers.
Himelstein BP. Himelstein BP. Curr Opin Oncol. 1998 Jul;10(4):326-33. doi: 10.1097/00001622-199807000-00009. Curr Opin Oncol. 1998. PMID: 9702400 Review.
Biologically, the area of interest on chromosome 3q, which may contain an osteosarcoma tumor suppressor gene, is being narrowed, and several promising new therapeutic approaches including tumor vaccine have been explored. In chondrosarcoma research, abnormalities in hereditary …
Biologically, the area of interest on chromosome 3q, which may contain an osteosarcoma tumor suppressor gene, is being narrowed, and several …
Dedifferentiated chondrosarcoma in patients with multiple osteochondromatosis: report of a case and review of the literature.
Kilpatrick SE, Pike EJ, Ward WG, Pope TL. Kilpatrick SE, et al. Skeletal Radiol. 1997 Jun;26(6):370-4. doi: 10.1007/s002560050250. Skeletal Radiol. 1997. PMID: 9229421 Review.
Multiple osteochondromatosis (MOS) is a familial disorder of autosomal dominant transmission characterized by the development of multiple exostoses and often derangements of epiphyseal cartilage, sometimes resulting in long bone growth retardati …
Multiple osteochondromatosis (MOS) is a familial disorder of autosomal dominant transmission characterized by the development of m …
Proteus syndrome: a newly recognized hamartomatous syndrome with significant craniofacial dysmorphology.
Tattelbaum AG, Dufresne CR. Tattelbaum AG, et al. J Craniofac Surg. 1995 Mar;6(2):151-60. J Craniofac Surg. 1995. PMID: 8601022 Review.
A new disorder describing multiple hamartomas distinct from neurofibromatosis and Klippel-Trenaunay-Weber syndrome was first reported in 1979. ...The clinical manifestations are extensive, including cranial exostoses; progressive enlargement, asymmetry and disfigure …
A new disorder describing multiple hamartomas distinct from neurofibromatosis and Klippel-Trenaunay-Weber syndrome was first reported …