Exploring the Origin of Cells in the Progression of Primary Myelofibrosis to Acute Myeloid Leukemia Case Report.

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2026-06-09 eCollection Date: 2026-01-01 DOI:10.1155/crh/5472609
Philip Papayanis, Kara Conroy, Melissa Larson, Sunita Nathan, Celalettin Ustun
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引用次数: 0

Abstract

Primary myelofibrosis (PMF) is the clonal proliferation of common myeloid progenitor (CMP) cells and can transform into acute myeloid leukemia (AML). The exact transformation process and cell lines involved are not well-understood. A patient with PMF received an allogenic hematopoietic stem cell transplant (alloHCT) from his major ABO incompatible sibling and developed pure red cell aplasia that resolved when his blood type switched to that of his donor's. He relapsed with AML 10 months after alloHCT; interestingly, his blood type remained his donor's type. This supports that AML in this patient with PMF stemmed from more committed progenitors (myeloblasts) than CMP.

原发性骨髓纤维化发展为急性髓系白血病的细胞起源探讨。
原发性骨髓纤维化(PMF)是普通髓系祖细胞(CMP)的克隆性增殖,可转化为急性髓系白血病(AML)。确切的转化过程和所涉及的细胞系尚不清楚。一位患有PMF的患者接受了来自ABO血型不相容的兄弟姐妹的同种异体造血干细胞移植(alloHCT),并出现了纯粹的红细胞发育不全,当他的血型与供者的血型转换后,这种情况就消失了。同种异体hct后10个月AML复发;有趣的是,他的血型仍然是捐赠者的血型。这支持该PMF患者的AML起源于比CMP更坚定的祖细胞(髓母细胞)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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51
审稿时长
13 weeks
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