Literature DB >> 6431885

Rhabdomyosarcoma of the temporal bone.

W D Chasin.   

Abstract

The temporal bone is the primary site for approximately 10% of rhabdomyosarcomas of the head and neck in children. Until recently it has been a uniformly fatal tumor despite treatment with radical surgery and radiation therapy. Although experience with the Intergroup Rhabdomyosarcoma Study protocol-II is of relatively short duration, treatment of these children with radiation therapy and multiple-drug intravenous and intrathecal chemotherapy holds promise of significantly improved control rates.

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Year:  1984        PMID: 6431885     DOI: 10.1177/00034894840930s413

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol Suppl        ISSN: 0096-8056


  2 in total

1.  Expanding the Spectrum of Intraosseous Rhabdomyosarcoma: Correlation Between 2 Distinct Gene Fusions and Phenotype.

Authors:  Narasimhan P Agaram; Lei Zhang; Yun-Shao Sung; Marcela S Cavalcanti; Dianne Torrence; Leonard Wexler; Glenn Francis; Scott Sommerville; David Swanson; Brendan C Dickson; Albert J H Suurmeijer; Richard Williamson; Cristina R Antonescu
Journal:  Am J Surg Pathol       Date:  2019-05       Impact factor: 6.394

2.  Rhabdomyosarcoma of the temporal bone: clinical report.

Authors:  R Cemiloğlu; S A Tekalan; T Patiroglu; Y Unlü
Journal:  Arch Otorhinolaryngol       Date:  1987
  2 in total

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