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Hemophagocytic syndrome: a rare complication of allogeneic nonmyeloablative hematopoietic stem cell transplantation.

机译:噬血细胞综合征:同种异体非清髓性造血干细胞移植的罕见并发症。

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摘要

We report two cases of patients with malignant lymphoma who presented with early onset of hemophagocytic syndrome after nonmyeloablative allogeneic peripheral blood stem cell transplantation. Fever and skin eruption developed early after transplantation, and neurological symptoms preceded cytopenia and worsened progressively. Activated macrophages with hemophagocytosis were found in bone marrow of the two patients at day 15 and 56, respectively. The fact that no obvious infectious agents associated with hemophagocytic syndrome were detected, and that serum soluble interleukin-2 receptor concentrations were elevated in the early phase after transplantation, reflecting the activation of donor-derived T cells, suggests that this complication resulted from an alloimmune response.
机译:我们报告了两例恶性淋巴瘤患者,这些患者在非清髓性同种异体外周血干细胞移植后出现了噬血细胞综合征的早期发作。移植后早期出现发热和皮肤喷发,神经症状先于血细胞减少,并逐渐恶化。分别在第15天和第56天在两名患者的骨髓中发现了具有吞噬作用的活化巨噬细胞。没有发现与噬血细胞综合征相关的明显感染因子,并且在移植后的早期血清可溶性白介素2受体浓度升高,这反映了供体来源的T细胞的活化这一事实表明,这种并发症是由同种免疫引起的。响应。

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