Liberato N L, Bollati P, Chiofalo F, Filipponi M, Poli M
Divisione di Medicina, Ospedale C. Mira, Casorate Primo, Italy.
Haematologica. 1996 Jan-Feb;81(1):40-43.
We report on a patient affected by multicentric Castleman's disease who developed an acute immunohemolytic anemia due to warm antibody. The clinical course was characterized by refractoriness to the steroidal treatment and by a dramatic improvement of the hematological and objective picture following combination chemotherapy (CHOP regimen). The possible existence of a link between the lymphoproliferative syndrome and the immunological derangement is also discussed.
我们报告了一例患有多中心Castleman病的患者，该患者因温抗体导致急性免疫性溶血性贫血。临床病程的特点是对类固醇治疗无效，而联合化疗（CHOP方案）后血液学和客观症状显著改善。我们还讨论了淋巴增殖综合征与免疫紊乱之间可能存在的联系。
