目的 :通过对血管免疫母细胞淋巴结病 ( AIL D)临床表现及辅助检查特点分析 ,为 AIL D诊治提供参考资料。方法 :回顾性分析 1 1例 AILD患者的临床资料。结果 :AIL D临床表现复杂 ,误诊率较高 ,确诊靠淋巴结活检 ,AIL D疗效较差。结论 :AILD必须靠淋巴结活检确诊 ,目前已被划为恶性疾病 ,尚无有效治疗方法 ,应该采取个体化的治疗原则 ,选用单一药物或者联合化疗进行治疗 Objective: To provide a reference for the diagnosis and treatment of AILD by analyzing the clinical manifestations of AILD and the features of auxiliary examinations. Methods: The clinical data of 11 AILD patients were retrospectively analyzed. Results: The clinical manifestations of AIL D were complex and the rate of misdiagnosis was high. The biopsy confirmed by lymph node biopsy showed poor efficacy of AIL D. Conclusion: AILD has to be diagnosed by lymph node biopsy. Currently, it has been classified as malignant disease. There is no effective treatment. AILD should adopt individualized treatment principle and choose single drug or combination chemotherapy