Donor Cell-Derived Myelodysplastic Syndrome Following Allogenic Peripheral Blood Stem Cell Transplant.

Ujjwala Narang, Sanjay Tewari
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Abstract

Donor cell-derived leukemia is a rare but well-described complication of allogeneic hematopoietic stem cell transplant (HSCT). This clinical case report aims to highlight the importance of recognizing this unusual disorder and thus, ensuring its appropriate management. We herein describe a case of a 9-year-old male diagnosed with acute lymphoblastic leukemia (ALL) and relapsed after initial chemotherapy. Subsequently, the patient had an allogenic peripheral blood stem cell transplant (PBSCT) from an HLA-matched, unrelated donor. Unfortunately, the patient then developed progressive thrombocytopenia, and following investigation, including bone marrow examination and cytogenetic analysis, he was diagnosed with donor cell-derived myelodysplastic syndrome. The literature review emphasizes the importance of considering it as a differential diagnosis of disease relapse following allogeneic HSCT.

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同种异体外周血干细胞移植后供体细胞源性骨髓增生异常综合征。
供体细胞源性白血病是一种罕见的异体造血干细胞移植(HSCT)并发症。本临床病例报告旨在强调认识这种不寻常的疾病的重要性,从而确保其适当的管理。我们在此描述一个9岁的男性诊断为急性淋巴细胞白血病(ALL)和复发后,最初的化疗。随后,患者接受了来自hla匹配的非亲属供体的同种异体外周血干细胞移植(PBSCT)。不幸的是,患者随后发展为进行性血小板减少症,经过调查,包括骨髓检查和细胞遗传学分析,他被诊断为供体细胞来源的骨髓增生异常综合征。文献综述强调了将其作为异基因造血干细胞移植后疾病复发的鉴别诊断的重要性。
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
32
审稿时长
12 weeks
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