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T-cell large granular lymphocytic leukemia occurring after autologous peripheral blood stem cell transplantation.

机译:自体外周血干细胞移植后发生T细胞大颗粒性淋巴细胞白血病。

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摘要

A 61-year-old man with angioimmunoblastic lymphoma in first complete remission underwent autologous peripheral blood stem cell transplantation. At 1 month post transplant, asymptomatic large granular lymphocytosis developed. The surface marker profile of the cells was CD3+CD8+CD56-CD57+. The disease course was chronic and indolent. The patient remains in complete remission from angioimmunoblastic lymphoma more than 6 months post transplant with persistent large granular lymphocytosis (lymphocyte count, 5-15 x 10(9)/l). Although post transplantation T-cell lymphoproliferative disorders have mostly occurred in allogeneic transplantation recipients and presented as aggressive lymphomas/leukemias, we suggest that chronic indolent T-cell large granular lymphocytic leukemia can occur after autologous stem cell transplantation.
机译:一名首次完全缓解的患有血管免疫母细胞淋巴瘤的61岁男子接受了自体外周血干细胞移植。移植后1个月,无症状的大颗粒淋巴细胞增多。细胞的表面标志物分布是CD3 + CD8 + CD56-CD57 +。病程是慢性和顽固的。移植后6个月以上,患者持续完全粒状淋巴细胞增多(淋巴细胞计数,5-15 x 10(9)/ l),从血管免疫母细胞淋巴瘤完全缓解。尽管移植后T细胞淋巴细胞增生性疾病大多数发生在异体移植接受者中,并表现为侵袭性淋巴瘤/白血病,但我们建议自体干细胞移植后可发生慢性惰性T细胞大颗粒淋巴细胞性白血病。

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