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Synchronous multifocal osteosarcoma: Report of one case

  • Ming Horng Tsai
  • , Chao Ping Yang*
  • , Tang Her Jaing
  • , Hsin Nung Shih
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital
  • Chang Gung University

Research output: Contribution to journal › Journal Article › peer-review

1 Scopus citations

Abstract

Synchronous multifocal osteosarcoma (SMOS), defined as more than one bone lesion at presentation, is a rare variant form of osteosarcoma. The onset is usually in childhood or early adolescence without pulmonary metastasis. The prognosis has been dismal. Whether SMOS represents a true multicentic origin or merely bone-to-bone métastases remains controversial. Here, we report a case of SMOS in a 10-year-old girl, with the dominant primary sclerotic tumor arising from the right distal femur. Despite aggressive chemotherapy and limb salvage surgery, she died of progressive multiple axial skeletal and symmetrical metaphyseal long bone diseases within one year after diagnosis. No pulmonary metastasis was found before she died.

Original languageEnglish
Pages (from-to)146-149
Number of pages4
JournalZhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui
Volume47
Issue number3
StatePublished - 05 2006

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Metastasis
  • Multifocal osteosarcoma
  • Synchronous

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