Bartoli E, Massarelli G, Soggia G, Tanda F
Am J Clin Pathol. 1980 Mar;73(3):423-6. doi: 10.1093/ajcp/73.3.423.
A patient who had diffuse lymph node enlargement, fever, skin rashes, anemia and polyclonal hypergammaglobulinemia is described. Histologic examination of lymph nodes taken from different sites (cervical, axillary and inguinal) revealed the presence of giant lymph node hyperplasia. The liver and bone marrow showed a moderate lymphocytic and plasma cell infiltration. The clinical presentation of a multicentric variety of giant lymph node hyperplasia in the reported case is similar to the clinical features usually associated with angio-immunoblastic lymphadenopathy with dysproteinemia, indicating that these two disorders may be related and may affect the same organs and systems. Alternatively, this histologic reactive giant lymph node hyperplasia progressing with a rapid declivitous course can be considered distinctive of a separate entity.
描述了一名出现弥漫性淋巴结肿大、发热、皮疹、贫血和多克隆高球蛋白血症的患者。对取自不同部位(颈部、腋窝和腹股沟)的淋巴结进行组织学检查,发现存在巨大淋巴结增生。肝脏和骨髓显示有中度淋巴细胞和浆细胞浸润。该报告病例中多中心型巨大淋巴结增生的临床表现与通常与伴有蛋白异常血症的血管免疫母细胞性淋巴结病相关的临床特征相似,表明这两种疾病可能相关,且可能影响相同的器官和系统。或者,这种组织学上呈反应性的巨大淋巴结增生以快速下降的病程进展可被视为一个独立实体的特征。