Maier H C, Sommers S C
J Thorac Cardiovasc Surg. 1980 Jun;79(6):860-3.
An adolescent girl with retarded development, delayed puberty, and hypergammaglobulinemia had anemia unresponsive to iron therapy that was cured when a mass of mediastinal giant lymph node hyperplasia was removed surgically. Rapid growth and development of secondary sexual characteristics occurred after operation. Follow-up studies made 20 years after operation showed compensated increased erythrocyte hemolysis and increased serum IgM. When mediastinal giant lymph node hyperplasia with abundant plasma cells is seen in childhood, there may be refractory anemia and immune disturbances. Similar giant lymph node hyperplasia without plasma cells may be found in an asymptomatic child or adult. The pertinent features of the few symptomatic cases reported are reviewed.
一名发育迟缓、青春期延迟且患有高球蛋白血症的青春期女孩患有对铁剂治疗无反应的贫血,在手术切除纵隔巨大淋巴结增生肿块后贫血得以治愈。术后出现了第二性征的快速生长和发育。术后20年的随访研究显示红细胞溶血代偿性增加以及血清IgM升高。当在儿童期发现伴有大量浆细胞的纵隔巨大淋巴结增生时,可能会出现难治性贫血和免疫紊乱。在无症状儿童或成人中可能会发现无浆细胞的类似巨大淋巴结增生。本文回顾了所报道的少数有症状病例的相关特征。