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连续急性髓系白血病患者接受正常供者血细胞治疗后的移植物抗宿主病

Graft-versus-host disease in consecutive patients with acute myeloid leukaemia treated with blood cells from normal donors.

作者信息

Lowenthal R M, Menon C, Challis D R

出版信息

Aust N Z J Med. 1981 Apr;11(2):179-83. doi: 10.1111/j.1445-5994.1981.tb04228.x.

Abstract

Two consecutive patients with acute myeloid leukaemia (AML) developed severe probable graft-versus-host disease (GVHD) following transfusion of blood products from normal donors. In one patient the AML had arisen de novo, while in the other it occurred four years after the patient developed non-Hodgkin's lymphoma (NHL) and was treated with radiotherapy and combination cytotoxic chemotherapy. Both patients received anti-leukaemic treatment with doxorubicin and cytosine arabinoside and intensive haematological supportive care with transfusions of red cell, white cell and platelet concentrates obtained from normal donors. Clinically the GVHD in each patient was manifest by a severe erythematous rash, intractable diarrhoea and abnormalities in the liver function tests. On pathological examination the skin in each case showed the typical changes of GVHD. Both patients died. There have been few previous reports of GVHD occurring after accidental engraftment of immunosuppressed patients undergoing therapy for acute leukaemia. Our experience suggests that it may occur more often than has hitherto been recognised. At present there is controversy concerning the possible anti-leukaemic effects of granulocyte transfusions. Until the relative importance of the benefits and deleterious effects of cells with the potential for engraftment is determined by further studies, we recommend the routine irradiation of all cellular blood products intended for administration to acute leukaemia patients undergoing intensive cytoreductive chemotherapy.

摘要

两名急性髓系白血病(AML)患者在输注正常供者的血液制品后发生了严重的可能的移植物抗宿主病(GVHD)。其中一名患者AML为原发性,另一名患者在患非霍奇金淋巴瘤(NHL)并接受放疗和联合细胞毒性化疗四年后发生AML。两名患者均接受了阿霉素和阿糖胞苷的抗白血病治疗,并接受了来自正常供者的红细胞、白细胞和血小板浓缩物输血的强化血液学支持治疗。临床上,每名患者的GVHD表现为严重的红斑皮疹、顽固性腹泻和肝功能检查异常。病理检查显示,每例患者的皮肤均呈现GVHD的典型变化。两名患者均死亡。此前很少有关于急性白血病免疫抑制患者意外植入后发生GVHD的报道。我们的经验表明,这种情况可能比迄今所认识到的更为常见。目前,关于粒细胞输血可能的抗白血病作用存在争议。在通过进一步研究确定具有植入潜力的细胞的益处和有害作用的相对重要性之前,我们建议对所有打算输给接受强化细胞减灭化疗的急性白血病患者的细胞血液制品进行常规辐照。

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