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成人急性淋巴细胞白血病的全血细胞减少前驱期(ALL前期):可能的发病机制

Pancytopenic prodrome (pre-ALL) of acute lymphoblastic leukemia in adults: possible pathogenesis.

作者信息

Sohn S K, Suh J S, Lee J, Lee K B

机构信息

Department of Clinical Pathology, Kyungpook National University Hospital, Taegu, Korea.

出版信息

Korean J Intern Med. 1998 Feb;13(1):64-7. doi: 10.3904/kjim.1998.13.1.64.

DOI:10.3904/kjim.1998.13.1.64
PMID:9538635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4531931/
Abstract

We report two cases of adult acute lymphoblastic leukemia presenting with preleukemic phase of pancytopenia with a few abnormal lymphoid cells in bone marrow aspirates. The initial diagnosis of each case was suspicious aplastic anemia and hypoplastic anemia. Both cases progressed to overt acute lymphoblastic leukemia within 1 year. We suggest that initial pancytopenic phase (pre-ALL) may precede the diagnosis of acute lymphoblastic leukemia in adults and differential diagnosis from myelodysplastic syndrome and primary aplastic anemia will be needed. We also suggest that primary bone marrow lymphoma and "primary unknown metastatic lymphoma of bone marrow" may be possible as the pathogenesis in a case like ours.

摘要

我们报告了两例成人急性淋巴细胞白血病,其表现为全血细胞减少的白血病前期,骨髓穿刺涂片中可见少量异常淋巴细胞。每例患者的初始诊断均为可疑再生障碍性贫血和增生低下性贫血。两例患者均在1年内进展为明显的急性淋巴细胞白血病。我们认为成人急性淋巴细胞白血病的诊断前可能存在初始全血细胞减少期(ALL前期),需要与骨髓增生异常综合征和原发性再生障碍性贫血进行鉴别诊断。我们还认为,在我们这样的病例中,原发性骨髓淋巴瘤和“原发性骨髓未知转移性淋巴瘤”可能是其发病机制。

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Korean J Intern Med. 1998 Feb;13(1):64-7. doi: 10.3904/kjim.1998.13.1.64.
2
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Transient pancytopenia preceding adult acute lymphoblastic leukemia with chromosomal abnormalities including the Philadelphia chromosome: A case report and review of the literature.伴有包括费城染色体在内的染色体异常的成人急性淋巴细胞白血病之前的短暂全血细胞减少症:一例报告并文献复习
Oncol Lett. 2015 Dec;10(6):3789-3792. doi: 10.3892/ol.2015.3766. Epub 2015 Sep 29.

本文引用的文献

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Childhood acute lymphoblastic leukaemia presenting with relapsing hypoplastic anaemia: progression of the same abnormal clone.以复发性再生障碍性贫血为表现的儿童急性淋巴细胞白血病:同一异常克隆的进展
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