Kunitomi Akane, Ishikawa Takayuki, Tajima Kenichirou, Konaka Yoshiteru, Yagita Masato
Division of Hematology and Rheumatology, Department of Medicine, Kitano Hospital, The Tazuke Kofukai Medical Research Institute, Osaka, Japan.
Int J Hematol. 2006 Apr;83(3):262-5. doi: 10.1532/IJH97.05148.
We describe a patient with Wegener granulomatosis (WG) who underwent long-term cyclophosphamide treatment and thereafter developed acute myelogenous leukemia (AML). After the AML was induced into remission, the patient received an allogeneic stem cell transplant (allo-SCT) from his sibling after undergoing a reduced-intensity conditioning regimen. His clinical course shortly after allo-SCT was uneventful. No clinically apparent acute or chronic graft-versus-host disease developed. Repeated analysis of the peripheral blood lymphocytes after transplantation showed complete donor chimerism. The level of proteinase 3 antineutrophil cytoplasmic antibody (PR3-ANCA) remained undetectable until 4 months after transplantation, when it began to increase. When the level of PR3-ANCA peaked, the patient suddenly presented with fever and joint pain, which later spontaneously resolved in parallel with the declining titer of PR3-ANCA. He is now in remission for both AML and WG at 22 months after transplantation. The patient's clinical course after allo-SCT may provide us with valuable information regarding the establishment of allo-SCT as a therapeutic option for WG.
我们描述了一名患有韦格纳肉芽肿(WG)的患者,该患者接受了长期环磷酰胺治疗,随后发生了急性髓系白血病(AML)。在AML诱导缓解后,该患者在接受减低强度预处理方案后接受了来自其同胞的异基因干细胞移植(allo-SCT)。allo-SCT后不久他的临床过程平稳。未发生临床上明显的急性或慢性移植物抗宿主病。移植后对外周血淋巴细胞的反复分析显示完全供体嵌合。蛋白酶3抗中性粒细胞胞浆抗体(PR3-ANCA)水平在移植后4个月一直未检测到,之后开始升高。当PR3-ANCA水平达到峰值时,患者突然出现发热和关节疼痛,随后随着PR3-ANCA滴度下降而自行缓解。移植后22个月时,他目前的AML和WG均处于缓解状态。该患者allo-SCT后的临床过程可能为我们提供有关将allo-SCT确立为WG治疗选择的有价值信息。