Literature DB >> 6272116

Sarcomas of bone in childhood: pathologic aspects.

J M Kissane, F B Askin, M E Nesbit, T J Vietti, E O Burgert, A Cangir, E A Gehan, C A Perez, D J Pritchard, M Tefft.   

Abstract

Some sarcomas of bone are not characteristically childhood tumors. Within the context of osteosarcomas, telangiectatic and parosteal (juxtacortical) variants deserve recognition. Among chondrosarcomas, which ordinarily are not tumors that occur in children, the mesenchymal variant should be recognized in children especially, this lesion may be extraosseous. Fibrous histiocytoma and its malignant variant have recently emerged as morphologically specific lesions, occasionally osseous, among other spindle cell tumors. Ewing's sarcoma, which is predominantly of osseous origin, consists of undifferentiated fragile cells. The elaborate spectrum of topographic, cytologic, nuclear, and other morphologic features that fall within the designation Ewing's sarcoma are described.

Entities:  

Mesh:

Year:  1981        PMID: 6272116

Source DB:  PubMed          Journal:  Natl Cancer Inst Monogr        ISSN: 0083-1921


  3 in total

1.  Basic fibroblast growth factor as a growth inhibitor for cultured human tumor cells.

Authors:  L Schweigerer; G Neufeld; D Gospodarowicz
Journal:  J Clin Invest       Date:  1987-11       Impact factor: 14.808

2.  Roentgenographic-pathologic correlation of diffuse sclerosis in Ewing sarcoma of bone.

Authors:  S K Shirley; L A Gilula; G P Siegal; M A Foulkes; J M Kissane; F B Askin
Journal:  Skeletal Radiol       Date:  1984       Impact factor: 2.199

3.  Ewing's sarcoma. A retrospective study of histological and immunohistochemical factors and their relation to prognosis.

Authors:  S Daugaard; C Kamby; L M Sunde; O Myhre-Jensen; T Schiødt
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1989
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.