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原发性肝脾T细胞淋巴瘤三例报告并文献复习 被引量:2

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摘要 目的探讨原发性肝脾T细胞淋巴瘤的临床表现、病理学特征和免疫表型特点。方法对3例原发性肝脾T细胞淋巴瘤患者的临床资料进行回顾性分析并对相关文献进行复习。结果患者肝脾明显大,伴有发热、全血细胞减少及肝功能受损;病理示瘤细胞弥漫浸润肝/脾脏红髓血窦;免疫表型:瘤细胞表达CD+2、CD+3、CD-4、CD-8,TCR-γ/δ(+)。结论肝脾T细胞淋巴瘤是较为罕见的外周T细胞淋巴瘤,预后较差,应注意与恶性组织细胞病鉴别。
出处 《白血病.淋巴瘤》 CAS 2006年第2期137-138,共2页 Journal of Leukemia & Lymphoma
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参考文献9

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共引文献55

同被引文献8

  • 1Shuan-ZengWei,Tong-HuaLiu,De-TianWang,Jin-LingCao,Yu-FengLuo,Zhi-YongLiang.Hepatosplenic γδ T-cell lymphoma[J].World Journal of Gastroenterology,2005,11(24):3729-3734. 被引量:2
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  • 8魏拴增,刘彤华.肝脾γδT和αβT细胞淋巴瘤[J].中华病理学杂志,2003,32(1):62-64. 被引量:14

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