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Lennert（芮纳）氏淋巴瘤是少见的特殊淋巴瘤，国内仅有数例报道，但国外文献记载已近百例。本所1980年～1983年期间收治了两例、临床病理过程符合Lennert氏淋巴瘤的病例，现报道如下。例1，女性，44岁。颈部无痛性肿块2年，进行性增大半年于1980年11月26日首次入院。查体颈部、锁骨上窝，腹股沟淋巴结肿大0.5～4cm不等，血清免疫球蛋白定量（mg/ml）IgG1704、IgA56、IgM50，未治，自动出院。2年后病情加重，颈部肿块明显增大，伴畏寒发热再次入院。查体颈部、锁骨上窝、腹股沟淋巴结均明显增大，B超示“肝脾大，肝回声增多”，骨髓象微示感染。颈淋巴结活
Lennert’s lymphoma is a rare special lymphoma, only a few cases reported in China, but nearly 100 foreign literature records. Our hospital from 1980 to 1983 admitted to two cases, clinical and pathological process consistent with Lennert’s lymphoma cases are reported below. Example 1, female, 44 years old. Neck painless mass 2 years, progressive increase in six months on November 26, 1980 the first admission. Examination of the neck, supraclavicular fossa, inguinal lymph nodes 0.5 ~ 4cm range, serum immunoglobulin quantitative (mg / ml) IgG1704, IgA56, IgM50, untreated, discharged automatically. Two years later, the disease aggravated, the neck mass was significantly increased, with chills and fever re-admitted. Physical examination neck, supraclavicular fossa, inguinal lymph nodes were significantly increased, B ultrasound showed “hepatosplenomegaly, increased liver echo,” bone marrow micrometeorosis. Cervical lymph node activity