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- Ihara Tatsuya
- Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
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- Okamura Daisuke
- Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
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- Takahashi Naoki
- Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
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- Kohri Mika
- Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
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- Kayano Hidekazu
- Department of Pathology, Saitama Medical University
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- Tamaru Jun-ichi
- Department of Pathology, Saitama Medical University
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- Niitsu Nozomi
- Department of Hematology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University
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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
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- Journal of Clinical and Experimental Hematopathology
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Journal of Clinical and Experimental Hematopathology 48 (2), 61-64, 2008
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詳細情報 詳細情報について
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- CRID
- 1390282679676885888
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- NII論文ID
- 10023917300
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- NII書誌ID
- AA11556796
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- ISSN
- 18809952
- 13464280
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可