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异基因造血干细胞移植后供者来源的弥漫大 B 细胞淋巴瘤:急性髓系白血病病例报告

Donor-derived diffuse large B-cell lymphoma after haploidentical stem cell transplantation for acute myeloid leukemia.

机构信息

Department of Hematology, Toyama Red Cross Hospital, Toyama, Japan.

Division of Diagnostic Pathology, Toyama Red Cross Hospital, Toyama, Japan.

出版信息

J Clin Exp Hematop. 2022;62(3):175-180. doi: 10.3960/jslrt.22014.

Abstract

We report a case of donor-derived diffuse large B-cell lymphoma (DLBCL), which developed 5 years after stem cell transplantation from a human leukocyte antigen (HLA)-haploidentical donor for acute myeloid leukemia (AML). A 51-year-old male was diagnosed with AML with variant KMT2A translocation involving t(6;11)(q13;q23). After 12 cycles of azacitidine treatment, fluorescence in situ hybridization (FISH) for KMT2A split signal indicated that 94% of his bone marrow (BM) cells were positive. He underwent peripheral blood stem cell transplantation (PBSCT) from his HLA-haploidentical son. The preconditioning regimen consisted of fludarabine, busulfan, melphalan, and antithymocyte globulin (ATG). The graft-versus-host disease (GVHD) prophylaxis consisted of tacrolimus and short-term methotrexate. On day 28, KMT2A FISH analysis indicated that he had achieved a complete response (CR). He continued to receive tacrolimus for the limited type of cutaneous chronic GVHD. Five years after the transplantation, positron emission tomography/computed tomography (PET/CT) showed an abdominal tumor. The tumor was diagnosed as DLBCL without Epstein-Barr virus. BM aspiration revealed the infiltration of lymphoma cells with t(8;14)(q24;q32). Chimerism analysis showed that both the peripheral blood (PB) and abdominal lymphoma cells were of donor origin. After 4 cycles of salvage chemotherapy, PET/CT showed that a CR had been achieved. He underwent a second PBSCT from an HLA-identical unrelated donor. The preconditioning regimen and GVHD prophylaxis were the same as those for the first PBSCT without ATG. The patient's PB revealed complete second donor-type chimerism, and the patient has maintained a CR since the second transplantation.

摘要

我们报告了一例 5 年前因急性髓系白血病(AML)接受 HLA 单倍体相合供者造血干细胞移植后发生供体来源弥漫性大 B 细胞淋巴瘤(DLBCL)的病例。一名 51 岁男性被诊断为 AML,伴 KMT2A 易位,涉及 t(6;11)(q13;q23)。接受 12 周期阿扎胞苷治疗后,KMT2A 分裂信号荧光原位杂交(FISH)显示其骨髓(BM)细胞中有 94%呈阳性。他接受了来自 HLA 单倍体相合儿子的外周血造血干细胞移植(PBSCT)。预处理方案包括氟达拉滨、白消安、马法兰和抗胸腺细胞球蛋白(ATG)。移植物抗宿主病(GVHD)预防方案包括他克莫司和短期甲氨蝶呤。第 28 天,KMT2A FISH 分析显示他已达到完全缓解(CR)。他继续接受他克莫司治疗局限性皮肤慢性 GVHD。移植后 5 年,正电子发射断层扫描/计算机断层扫描(PET/CT)显示腹部肿瘤。肿瘤诊断为无 EBV 的 DLBCL。BM 抽吸显示淋巴瘤细胞浸润伴 t(8;14)(q24;q32)。嵌合分析显示外周血(PB)和腹部淋巴瘤细胞均来源于供者。4 周期挽救化疗后,PET/CT 显示 CR 已达到。他接受了来自 HLA 完全相合无关供者的第二次 PBSCT。预处理方案和 GVHD 预防方案与第一次 PBSCT 相同,不使用 ATG。患者的 PB 显示完全的第二次供者型嵌合体,自第二次移植以来,患者一直保持 CR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/404d/9635034/2439bfd9d3ae/jslrt-62-175-g001.jpg

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