Alveolar Rhabdomyosarcoma Mimicking Nasal Lymphoma at The Initial Presentation

  • Ihara Tatsuya
    Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
  • Okamura Daisuke
    Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
  • Takahashi Naoki
    Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
  • Kohri Mika
    Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
  • Kayano Hidekazu
    Department of Pathology, Saitama Medical University
  • Tamaru Jun-ichi
    Department of Pathology, Saitama Medical University
  • Niitsu Nozomi
    Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University

この論文をさがす

抄録

Rhabdomyosarcoma is exceedingly rare in adults. A 62-year-old woman was referred to our hospital because of general pain. Computed tomography revealed a solid tumor in the right nasal cavity. Histopathological examination showed solid proliferation of atypical small round cells, having cytologic features reminiscent of lymphomas, and lacking the fibrovascular stroma. The cells were CD56+, desmin+, vimentin+, HHF35+, myogenin+ and MyoD1+. The patient was positive for the PAX3-FKHR fusion gene. The patient was diagnosed as having alveolar rhabdomyosarcoma. We conclude that rhabdomyosarcoma should be included in the differential diagnoses of CD56+ small round cell tumor, and immunohistochemical and cytogenetic studies should be performed. [J Clin Exp Hematopathol 48(2) : 61-64, 2008]

収録刊行物

参考文献 (21)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ