Primary Hepatic Ewing’s Sarcoma with Cytogenetic Confirmation
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  • 作者:P. F. McGrann (1)
    I. J. Pooleman (1)
    C. H. Wilson (1)
    B. Haugk (2)
    J. Scott (3)
    R. M. Charnley (1)
  • 关键词:Ewing’s sarcoma ; Hepatic mass ; Cytogenetic diagnosis
  • 刊名:Journal of Gastrointestinal Surgery
  • 出版年:2014
  • 出版时间:March 2014
  • 年:2014
  • 卷:18
  • 期:3
  • 页码:635-637
  • 全文大小:258 KB
  • 参考文献:1. Pinto A, Dickman P, Parham D: Pathobiologic markers of the Ewing sarcoma family of tumors: state of the art and prediction of behaviour. Sarcoma 2011;2011:856190. CrossRef
    2. Applebaum MA, Worch J, Matthay KK, et al.: Clinical features and outcomes in patients with extraskeletal Ewing sarcoma. Cancer 2011;117:3027-032. CrossRef
    3. Ahmad R, Mayol BR, Davis M, et al.: Extraskeletal Ewing’s sarcoma. Cancer 1999;85:725-31. CrossRef
    4. Mani S, Dutta D, De BK: Primitive neuroectodermal tumor of the liver: a case report. Jpn J Clin Oncol 2010;40:258-62. CrossRef
    5. Balasubramanian SK, Jittiwat J, Manikandan J, et al.: Biodistribution of gold nanoparticles and gene expression changes in the liver and spleen after intravenous administration in rats. Biomaterials 2010;31:2034-042. CrossRef
    6. Marques M, Cardoso H, Barroca H, et al.: Peripheral primitive neuroectodermal tumour of the liver: a case report and review of the literature. Gastroenterol Hepatol 2011;34:611-13. CrossRef
    7. Cambruzzi E, Guerra EE, Hilgert HC, et al.: Primitive neuroectodermal tumor of the liver: a case report. Case Report Med 2011;2011:748194.
    8. Verrill MW, Judson IR, Harmer CL, et al.: Ewing’s sarcoma and primitive neuroectodermal tumor in adults: are they different from Ewing's sarcoma and primitive neuroectodermal tumor in children? J Clin Oncol 1997;15:2611-621.
    9. Tural D, Molinas Mandel N, Dervisoglu S, et al.: Extraskeletal Ewing’s sarcoma family of tumors in adults: prognostic factors and clinical outcome. Jpn J Clin Oncol 2012;42:420-26. CrossRef
    10. Kallala R, Nikkhah D, Nix P, et al.: Primary extraskeletal Ewing sarcoma involving the carotid artery: a case report and review of the current literature. Ann R Coll Surg Engl 2012;94:141-43. CrossRef
  • 作者单位:P. F. McGrann (1)
    I. J. Pooleman (1)
    C. H. Wilson (1)
    B. Haugk (2)
    J. Scott (3)
    R. M. Charnley (1)

    1. Department of Hepatopancreaticobiliary Surgery, The Freeman Hospital, Freeman Road, High Heaton, Newcastle upon Tyne, UK, NE7 7DN
    2. Department of Cellular Pathology, The Royal Victoria Infirmary, Newcastle upon Tyne, UK
    3. Department of Radiology, The Freeman Hospital, Newcastle upon Tyne, UK
  • ISSN:1873-4626
文摘
Introduction Extraskeletal Ewing’s sarcoma is reported in the medical literature, but none has been described as presenting with a resectable liver mass. Methods A case of a 29-year-old male patient who presented with a large symptomatic mass in the right lobe of the liver which, following resection, demonstrated the characteristic histopathology and fusion protein (EWSR1-Fli1) found in Ewing’s sarcoma was reported. Discussion Complete surgical resection offers the best long-term outlook. Cure rates with appropriate surgical and chemotherapeutic management range between 30 and 60 %.

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