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成人急性淋巴细胞白血病伴骨髓再生障碍

Adult acute lymphoblastic leukaemia presenting with bone marrow aplasia.

作者信息

Dharmasena F, Littlewood T, Gordon-Smith E C, Catovsky D, Galton D A

出版信息

Clin Lab Haematol. 1986;8(4):361-4. doi: 10.1111/j.1365-2257.1986.tb00124.x.

DOI:10.1111/j.1365-2257.1986.tb00124.x
PMID:3466737
Abstract

We report two adult patients who presented with bone marrow aplasia and latterly were diagnosed to have acute lymphoblastic leukaemia (ALL). Although the aplastic presentation of ALL in childhood is well documented it has not been previously reported in adult ALL. The mechanism of this presentation is unclear. In one of our patients folate deficiency appears to have been the cause.

摘要

我们报告了两名成年患者,他们最初表现为骨髓再生障碍,后来被诊断为急性淋巴细胞白血病(ALL)。尽管儿童ALL的再生障碍表现已有充分记录,但此前在成人ALL中尚未有过报道。这种表现的机制尚不清楚。在我们的一名患者中,叶酸缺乏似乎是病因。

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Adult acute lymphoblastic leukaemia presenting with bone marrow aplasia.成人急性淋巴细胞白血病伴骨髓再生障碍
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Routine bone marrow examination in the management of acute lymphoblastic leukaemia of childhood.儿童急性淋巴细胞白血病治疗中的常规骨髓检查
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The aplastic presentation of childhood leukaemia: a feature of common-ALL.儿童白血病的再生障碍性表现:普通型急性淋巴细胞白血病的一个特征
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Acute lymphoblastic leukaemia presenting as aplastic anaemia.表现为再生障碍性贫血的急性淋巴细胞白血病。
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Uterine and ovarian leukaemic relapse during bone marrow remission in acute lymphoblastic leukaemia.急性淋巴细胞白血病骨髓缓解期出现子宫和卵巢白血病复发。
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引用本文的文献

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Spontaneous remission of acute lymphoblastic leukemia: A case report.急性淋巴细胞白血病的自发缓解:一例报告。
Oncol Lett. 2018 Jan;15(1):115-120. doi: 10.3892/ol.2017.7288. Epub 2017 Oct 30.
2
Pancytopenia - (?) An obstacle in the diagnosis and outcome of pediatric acute lymphoblastic leukemia.全血细胞减少症——(?)小儿急性淋巴细胞白血病诊断及预后的一个障碍。
South Asian J Cancer. 2015 Apr-Jun;4(2):68-71. doi: 10.4103/2278-330X.155648.
3
Pancytopenic prodrome (pre-ALL) of acute lymphoblastic leukemia in adults: possible pathogenesis.
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
Korean J Intern Med. 1998 Feb;13(1):64-7. doi: 10.3904/kjim.1998.13.1.64.
4
Aplastic presentation of acute lymphoblastic leukemia.急性淋巴细胞白血病的再生障碍性表现。
J R Soc Med. 1987 Jul;80(7):465.