异基因造血干细胞移植后的供体细胞白血病。

IF 1.3 Q4 HEMATOLOGY
Journal of hematology Pub Date : 2023-06-01 Epub Date: 2023-06-30 DOI:10.14740/jh1124
Ahmed Khattab, Sunita Patruni, Gina Patrus, Yazan Samhouri, Salman Fazal, John Lister
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引用次数: 0

摘要

全世界每年进行大约25000例同种异体移植;这一数字在过去三十年中稳步上升。移植受体存活率的研究已成为一个令人信服的话题,移植后供体细胞病理学值得进一步研究。供体细胞白血病(DCL)是异基因干细胞移植(SCT)的一种罕见但严重的并发症,受体发展为源于用于移植的供体细胞的白血病。预测供体细胞病理学的异常检测可能会为供体的选择提供信息,而早期检测这些异常的存活计划的设计可能会允许在病程早期进行治疗干预。我们介绍了四名来自我们机构的异基因造血干细胞移植(HSCT)接受者,他们出现了供体细胞异常的异基因SCT,强调了他们的临床特征和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Donor Cell Leukemia Following Allogeneic Hematopoietic Stem Cell Transplantation.

Approximately 25,000 allogeneic transplants are performed annually worldwide; a figure that has steadily increased over the past three decades. The study of transplant recipient survivorship has become a cogent topic and post-transplant donor cell pathology warrants further study. Donor cell leukemia (DCL) is a rare but serious complication of allogeneic stem cell transplantation (SCT) where the recipient develops a form leukemia originating from the donor cells used for transplantation. Detection of abnormalities predicting donor cell pathology might inform donor selection, and the design of survivorship programs for early detection of these abnormalities might allow therapeutic intervention earlier in the disease course. We present four recipients of allogeneic hematopoietic stem cell transplant (HSCT) from our institution who developed donor cell abnormalities allogeneic SCT, highlighting their clinical characteristics and challenges.

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Journal of hematology
Journal of hematology HEMATOLOGY-
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