论文部分内容阅读
嗜酸性淋巴肉芽肿即Kimura’s病(KD)是一种少见的、原因不明的、多累及头颈部浅表淋巴结及软组织的慢性肉芽肿病变。该病多发于亚洲男性。头颈部多发性嗜酸性淋巴肉芽肿对患者身体健康构一定程度威胁[1]。因此,如何有效的诊治头颈部多发性嗜酸性淋巴肉芽肿成为临床关注的焦点问题,在这里以在2011年11月至2013年11月期间收治的2例头颈部多发性嗜酸性淋巴肉芽肿患者作为研究对象,探讨头颈部多发性嗜酸性淋巴肉芽肿临床特征及治疗,现报告如下。“,”Eosinophilic Lymphoid Granuloma, namely s Kimura disease (KD), is a rare, unexplained, chronic granuloma lesion of the superficial lymph nodes and soft tissues of the head and neck. The disease is frequently occurring in Asia. The structure of the multiple eosinophilic granuloma of the head and neck is threatening to the physical health of the patients [1]. Therefore, how effective the treatment of head and neck of multiple addicted to acidic lymphogranuloma become the focus of clinical attention, here to in November 2011 to November 2013 admitted during the period of 2 cases of head and neck multiple addicted to acidic lymphogranuloma patients as the research object of head and neck acid is lymphatic granulation is swollen, clinical features and treatment of eosinophilic, report as follows now.