Bradley S L, Dines D E, Banks P M, Hill R W
Chest. 1981 Sep;80(3):312-8. doi: 10.1378/chest.80.3.312.
Immunoblastic lymphadenopathy presents with fever, malaise, cough, dyspnea, lymphadenopathy, hepatosplenomegaly, hypergammaglobulinemia, interstitial pulmonary infiltrates, mediastinal adenopathy, and effusions. The diagnosis is made on the basis of lymph node biopsy. Based on the course in our patients and the cases presented in previous reports, a suggested program of treatment for immunoblastic lymphadenopathy includes administration of moderate doses of steroids initially, with a subsequent increase to a higher dosage if desired improvement does not occur. Chemotherapy with three drugs, cyclophosphamide, vincristine, and prednisone, is indicated if remission using steroids fails. The diagnostic dilemma of whether pulmonary infiltrates are due to the disease itself or to pulmonary infection or to cytotoxic changes from chemotherapy always exists and often requires specimens from either transbronchoscopic or open-lung biopsy for definitive diagnosis and treatment.
免疫母细胞性淋巴结病表现为发热、不适、咳嗽、呼吸困难、淋巴结病、肝脾肿大、高球蛋白血症、间质性肺浸润、纵隔淋巴结病及胸腔积液。诊断基于淋巴结活检。根据我们患者的病程及既往报告中的病例,免疫母细胞性淋巴结病的建议治疗方案包括初始给予中等剂量的类固醇,如果未出现预期改善则随后增加至更高剂量。如果使用类固醇治疗未能缓解,则需使用环磷酰胺、长春新碱和泼尼松三种药物进行化疗。肺部浸润是由疾病本身、肺部感染还是化疗引起的细胞毒性改变导致的诊断难题一直存在,通常需要经支气管镜或开胸肺活检获取标本以进行明确诊断和治疗。