Lennert淋巴瘤是近几年才确定的一特殊类型的淋巴瘤。首先由德国学者Lennert和Metdagh(1968)报导30例,病变特点是存在多量类上皮细胞又缺乏典型的李-史细胞,临床表现也与一般何杰金氏病不同,发病年龄主要是中年以上,易侵犯扁桃体和脾脏。1975年作者进一步明确性质,并称为“淋巴类上皮细胞性淋巴瘤”。列入非何杰金氏淋巴瘤范围。美国学者Burke和Butler(1976)亦报导15例组织学改变相似于雷芮氏报告的病例,提名为雷芮氏淋巴瘤。近三年多来关于此类淋巴瘤的病例陆续有报道,现将收集的有关资料分三方面扼要介绍。 Lennert lymphoma is a special type of lymphoma that has been identified in recent years. Firstly, 30 cases were reported by German scholars Lennert and Metdagh (1968). The lesions were characterized by the presence of a large number of epithelial cells and a lack of typical Lee-history cells. The clinical manifestations were also different from those of Hodgkin’s disease in general. The onset age was mainly above middle age. , easy to invade the tonsils and spleen. In 1975, the author further defined the nature and called “lymphoid epithelial cell lymphoma.” Included in non-Hodgkin lymphomas. American scholars Burke and Butler (1976) also reported 15 cases of histological changes similar to those reported by Raytheon and nominated as Ray’s lymphoma. Over the past three or more years, there have been reports of such cases of lymphoma. The collected data are summarized in three parts.