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淋巴瘤样肉芽肿的临床病理特点 被引量：7

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摘要 在2004年版WHO肺肿瘤组织学分类中，将淋巴瘤样肉芽肿（lymphomatoid granulomatosis，LG）肿瘤细胞定义为Epstein—Barr（EB）病毒阳性B细胞，伴有丰富的反应性T细胞，从良性、交界性到恶性（分Ⅰ、Ⅱ、Ⅲ级）呈谱系变化。Ⅲ级为弥漫性大B细胞淋巴瘤（DLBCL）的一种亚型，即为结外多系统和多器官受累的、富于T细胞的EB病毒阳性大B细胞淋巴瘤。该病变罕见，临床缺乏特异性，极易误诊或漏诊。我们对其临床、影像和病理学特点、认识变迁及发病机制等进行综述。
作者 何春年 张静 段国辰
机构地区 河北省人民医院病理科 河北省人民医院普通外科 河北省人民医院胸外科
出处 《中华病理学杂志》 CAS CSCD 北大核心 2007年第5期336-338,共3页 Chinese Journal of Pathology
关键词 淋巴瘤样肉芽肿 临床病理特点 大B细胞淋巴瘤 反应性T细胞 EB病毒 病理学特点 肿瘤组织 肿瘤细胞
分类号 R734.2 [医药卫生—肿瘤]
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参考文献26

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共引文献34

同被引文献61

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引证文献7

二级引证文献9

中华病理学杂志
2007年 第5期

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