Cho Seok Goo, Koh Yong Bok, Chang Hong Seok, Park Gyeongsin, Kang Chang Suk, Park Jong Won, Min Woo Sung
Department of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Eur J Haematol. 2005 Mar;74(3):259-62. doi: 10.1111/j.1600-0609.2004.00359.x.
A 25-yr-old man had been diagnosed as having CD30(+) anaplastic large cell lymphoma associated with hemophagocytic syndrome (HS). He received aggressive frontline chemotherapies and consolidation with autologous peripheral blood stem cell transplantation (PBSCT) following high-dose chemotherapy combined with splenic irradiation (720 cGy in fraction of 180 cGy). However, HS recurred on day 50 of PBSCT without radiologic evidence of lymphoma relapse. On day 56 of PBSCT, splenectomy was performed and pathology showed massive sinusoidal infiltration of histiocytes. On day 68 of PBSCT, administration of interferon alpha was started and maintained for 24 months. HS was completely resolved and he has been alive well and in complete remission (CR), 60 months after initial diagnosis.
一名25岁男性被诊断为患有与噬血细胞综合征(HS)相关的CD30(+)间变性大细胞淋巴瘤。他接受了积极的一线化疗,并在大剂量化疗联合脾脏照射(每次180 cGy,共720 cGy)后进行自体外周血干细胞移植(PBSCT)巩固治疗。然而,在PBSCT第50天时HS复发,而无淋巴瘤复发的影像学证据。在PBSCT第56天时进行了脾切除术,病理显示组织细胞大量窦状浸润。在PBSCT第68天时开始使用α干扰素并维持24个月。HS完全缓解,自初次诊断后60个月,他一直存活良好且处于完全缓解(CR)状态。