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费城染色体阳性急性髓系白血病经异基因造血干细胞移植成功治疗:病例报告及文献复习。

Philadelphia chromosome-positive acute myeloid leukemia successfully treated by allogeneic hematopoietic stem cell transplantation: A case report and review of the literature.

机构信息

Department of Hematology, The 940th Hospital of Joint Logistic Support Force of Chinese People's Liberation Army, Lanzhou, China.

First School of Clinical Medicine, Ningxia Medical University, Yinchuan, China.

出版信息

Medicine (Baltimore). 2024 May 10;103(19):e38110. doi: 10.1097/MD.0000000000038110.

DOI:10.1097/MD.0000000000038110
PMID:38728478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11081607/
Abstract

RATIONAL

The Philadelphia chromosome (Ph) is seen in most patients with chronic myeloid leukemia and some patients with acute lymphoblastic leukemia. However, Ph-positive acute myeloid leukemia (Ph + AML) is a rare entity with a poor prognosis and a short median survival period. To date, there have been few clinical reports on this disease. And the treatment regimen of this disease has not been uniformly determined.

PATIENT CONCERNS

We report a case of a Ph + AML. A 32-year-old male who was admitted to our hospital with weakness for 2 months.

DIAGNOSIS

Philadelphia chromosome-positive acute myeloid leukemia.

INTERVENTIONS

The patient achieved complete remission by the administration of a tyrosine kinase inhibitor, combined with low-intensity chemotherapy and a B-cell lymphoma 2 inhibitor. Then, allogeneic hematopoietic stem cell transplantation (allo-HSCT) from his sister was successfully performed.

OUTCOMES

The patient has been in a continuous remission state for 6 months after transplantation.

LESSONS

We reported a rare Ph + AML case, successfully treated with allo-HSCT. This case provided strong support for treating Ph + AML with allo-HSCT.

摘要

理性

费城染色体(Ph)见于大多数慢性髓性白血病患者和一些急性淋巴细胞白血病患者。然而,Ph 阳性急性髓系白血病(Ph+AML)是一种罕见的实体,预后不良,中位生存期短。迄今为止,关于这种疾病的临床报道很少。而且,这种疾病的治疗方案尚未统一确定。

患者关注

我们报告了一例 Ph+AML。一名 32 岁男性,因乏力 2 个月入住我院。

诊断

费城染色体阳性急性髓系白血病。

干预措施

该患者通过酪氨酸激酶抑制剂联合低强度化疗和 B 细胞淋巴瘤 2 抑制剂达到完全缓解。然后,他的姐姐成功地进行了异基因造血干细胞移植(allo-HSCT)。

结果

移植后 6 个月,患者持续缓解。

教训

我们报告了一例罕见的 Ph+AML 病例,成功地接受了 allo-HSCT 治疗。该病例为 allo-HSCT 治疗 Ph+AML 提供了有力支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a363/11081607/0aa553aa3bae/medi-103-e38110-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a363/11081607/760fe0a8edec/medi-103-e38110-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a363/11081607/0aa553aa3bae/medi-103-e38110-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a363/11081607/760fe0a8edec/medi-103-e38110-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a363/11081607/0aa553aa3bae/medi-103-e38110-g002.jpg

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本文引用的文献

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Leuk Res. 2023 Jan;124:107002. doi: 10.1016/j.leukres.2022.107002. Epub 2022 Dec 16.
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An adapted European LeukemiaNet genetic risk stratification for acute myeloid leukemia patients undergoing allogeneic hematopoietic cell transplant. A CIBMTR analysis.接受异基因造血细胞移植的急性髓系白血病患者的欧洲白血病网遗传风险分层适应。CIBMTR 分析。
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Antithymocyte Globulin for Matched Sibling Donor Transplantation in Patients With Hematologic Malignancies: A Multicenter, Open-Label, Randomized Controlled Study.
抗胸腺细胞球蛋白用于血液系统恶性肿瘤患者的同胞供者移植:一项多中心、开放标签、随机对照研究。
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4
Structure-based analysis and biological characterization of imatinib derivatives reveal insights towards the inhibition of wild-type BCR-ABL and its mutants.基于结构的分析和伊马替尼衍生物的生物学特性研究揭示了抑制野生型 BCR-ABL 及其突变体的新见解。
Bioorg Med Chem Lett. 2019 Dec 15;29(24):126758. doi: 10.1016/j.bmcl.2019.126758. Epub 2019 Oct 28.
5
Impact of an Additional Chromosome on the Clinical Outcomes of Hematopoietic Stem Cell Transplantation in Philadelphia Chromosome-Positive Acute Myeloid Leukemia in Adults.附加染色体对成人费城染色体阳性急性髓系白血病造血干细胞移植临床结局的影响。
Biol Blood Marrow Transplant. 2018 Aug;24(8):1621-1628. doi: 10.1016/j.bbmt.2018.04.020. Epub 2018 Apr 23.
6
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