Literature DB >> 9700767

[Cytogenetic and molecular genetic changes in malignant primary bone tumors].

A Zoubek1, H Kovar, H Gadner.   

Abstract

Osteosarcoma, chondrosarcoma and tumors of the Ewing group are the most frequently observed primary malignant bone tumors. In an Internet homepage recently constructed for the Orthopedic Hospital Rizzoli Bologna, Italy, these tumors have represented the majority of 4423 malignant bone tumors in the archives of this institution since 1920 (http:/(/)www.tizeta.it/rizzoli). Malignant fibrous histiocytoma, fibrosarcoma, hemangioendothelioma, malignant hemangiopericytoma and giant-cell tumors are diagnosed less frequently. Since the introduction of modern molecular and cytogenetic techniques, knowledge of genetic aberrations in malignant bone tumors has steadily increased. However, so far only for the group of Ewing tumors has a recurrent chromosomal marker, the translocation t(11;22) (q24;q12), been identified.

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Year:  1998        PMID: 9700767     DOI: 10.1007/s001170050381

Source DB:  PubMed          Journal:  Radiologe        ISSN: 0033-832X            Impact factor:   0.635


  1 in total

1.  Vaginal metastasis of a Ewing Sarcoma five years after resection of the primary tumor.

Authors:  Noemie Vanel; Victoire Vierling; Jennifer Kreshak; Marco Gambarotti; Stefania Cocchi; Cristina Tranfaglia; Daniel Vanel
Journal:  Clin Sarcoma Res       Date:  2011-08-01
  1 in total

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