新发作的细胞减少并不总是表明同种异体造血干细胞移植后复发的AML,这是一种非破坏性移植后淋巴细胞增生性疾病

IF 0.7 Q4 HEMATOLOGY
Süreyya Yiğit Kaya , Abdullah Emre Askin , Sebnem Bektas , Aslı Çakır , Ömür Gökmen Sevindik
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引用次数: 0

摘要

同种异体造血干细胞移植(allo-HSCT)仍然是治疗中高风险急性髓性白血病(AML)的有效选择。移植后淋巴细胞增生性疾病(PTLD)与移植后免疫抑制的强度有关。尽管eb病毒(EBV)血清阳性和再激活可能是PTLD的主要危险因素。一些PTLDs可能是EBV阴性。AML患者在HSCT后出现PTLD的病例非常有限。我们提出同种异体造血干细胞移植后细胞减少的鉴别诊断。这是首例AML患者在移植后较晚阶段发生骨髓ebv阴性PTLD的报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Newly onset cytopenias not always indicate a relapsing AML after allogeneic HSCT, a case of non-destructive post transplant lymphoproliferative disorder

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains an effective option for the treatment of intermediate and high-risk Acute myeloid leukemia (AML). Post-transplant lymphoproliferative disorder (PTLD) is related to the intensity of post-transplant immunosuppression. Although Epstein-Barr virus (EBV) seropositivity and reactivation can be a major risk factor for PTLD. A few PTLDs could be EBV negative. There are a very limited number of PTLD cases following HSCT in patients with AML. We present a differential diagnosis of cytopenias after allo-HSCT. This is the first report of an AML patient developing bone marrow EBV-negative PTLD relatively late in their post-transplant course.

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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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