Literature DB >> 24712008

[Diagnosis and treatment of childhood soft tissue sarcomas].

Rita Bánusz1, Zsófia Váradi1, Edit Varga1, Zsuzsa Jakab1, Miklós Garami1, Monika Csóka1.   

Abstract

Malignant tumors of mesenchymal origin are called sarcomas. Mesenchymal cells normally mature into skeletal muscle, smooth muscle, fat, fibrous tissue, bone and cartilage. Rhabdomyosarcoma (RMS) arises from immature mesenchymal cells that are committed to skeletal muscle lineage. However, it can also arise in tissues in which striated muscle is normally not found (such as the urinary tract). Undifferentiated sarcomas cannot be ascribed to any specific lineage. Treatment results improved significantly in the last decade by combined treatment (chemotherapy, surgery, irradiation, in some cases targeted therapy). Good treatment results can be achieved in pediatric oncology centers by early diagnosis and adequate treatment according to international treatment protocols.

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Year:  2014        PMID: 24712008

Source DB:  PubMed          Journal:  Magy Onkol        ISSN: 0025-0244


  1 in total

1.  [Clinical features and prognosis in 20 children with rhabdomyosarcoma].

Authors:  Si-Qin Liu; Fang-Hua Ye; Chen-Ying Fan; Min Peng; Jia-Jia Dong; Wen-Jun Deng; Hui Zhang; Yan Yu; Liang-Chun Yang
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2022 Sept 15
  1 in total

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