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自然杀伤细胞淋巴母细胞白血病/淋巴瘤:病例报告及近期文献综述

Natural Killer Cell Lymphoblastic Leukaemia/Lymphoma: Case Report and Review of the Recent Literature.

作者信息

Sedick Qanita, Alotaibi Sultan, Alshieban Saeed, Naheet Khalid Ben, Elyamany Ghaleb

机构信息

Department of Central Military Laboratory and Blood Bank, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.

Department of Adult Hematology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.

出版信息

Case Rep Oncol. 2017 Jul 7;10(2):588-595. doi: 10.1159/000477843. eCollection 2017 May-Aug.

DOI:10.1159/000477843
PMID:28868017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5567073/
Abstract

Natural killer (NK) cell lymphoblastic leukaemia/lymphoma is a rare haemopoietic tumour currently defined in the 2008 WHO classification under the category of acute leukaemias of ambiguous lineage. A diagnosis of this type of leukaemia is considered in cases expressing CD56 along with immature T-cell-associated markers such as CD2 and CD7 with absence of B-cell and myeloid markers; in addition, blastic plasmacytoid dendritic cell leukaemia should be excluded. Prior to 2008, these precursor NK cell lymphoblastic leukaemias/lymphomas were categorized as myeloid/NK cell acute leukaemia with a phenotype identical to acute myeloid leukaemia with minimal differentiation. While the new classification has merit in having excluded myeloid expression, there is still persistent confusion in the literature and on a practical level with regard to precursor NK cell neoplasms. There is a paucity of recent case reports in the literature after the new WHO classification of this neoplasm. Due to the rarity of this neoplasm, an accurate pathological diagnosis is often difficult. In this article, we describe a case of precursor NK cell lymphoblastic leukaemia/lymphoma presenting with unique morphological features and conflicting immunophenotypes. We also review all case reports of this neoplasm after the WHO 2008 classification.

摘要

自然杀伤(NK)细胞淋巴母细胞白血病/淋巴瘤是一种罕见的造血肿瘤,在2008年世界卫生组织分类中被归为急性白血病中谱系不明的一类。对于表达CD56以及不成熟T细胞相关标志物(如CD2和CD7)且缺乏B细胞和髓系标志物的病例,考虑诊断为此类白血病;此外,应排除浆细胞样树突状细胞白血病。在2008年之前,这些前体NK细胞淋巴母细胞白血病/淋巴瘤被归类为髓系/NK细胞急性白血病,其表型与分化极低的急性髓系白血病相同。虽然新分类在排除髓系表达方面有其优点,但在文献和实际应用中,对于前体NK细胞肿瘤仍存在持续的困惑。在世界卫生组织对该肿瘤进行新分类后,文献中近期的病例报告很少。由于这种肿瘤罕见,准确的病理诊断往往很困难。在本文中,我们描述了一例具有独特形态学特征和相互矛盾免疫表型的前体NK细胞淋巴母细胞白血病/淋巴瘤病例。我们还回顾了2008年世界卫生组织分类后该肿瘤的所有病例报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/d293c970020e/cro-0010-0588-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/6341635aed4e/cro-0010-0588-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/1c59fa12035e/cro-0010-0588-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/62000408e5d1/cro-0010-0588-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/d293c970020e/cro-0010-0588-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/6341635aed4e/cro-0010-0588-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/1c59fa12035e/cro-0010-0588-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/62000408e5d1/cro-0010-0588-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1011/5567073/d293c970020e/cro-0010-0588-g04.jpg

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本文引用的文献

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Brain Pathol. 2015 Jan;25(1):115-6. doi: 10.1111/bpa.12235.
2
Precursor NK cell lymphoblastic leukemia/lymphoma-report of a case with literature review.前驱NK细胞淋巴母细胞白血病/淋巴瘤——1例病例报告并文献复习
Indian J Hematol Blood Transfus. 2014 Sep;30(Suppl 1):283-5. doi: 10.1007/s12288-014-0360-x. Epub 2014 Mar 14.
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Five Chinese pediatric patients with leukemias possibly arising from immature natural killer cells: clinical features and courses.
Ann Transl Med. 2021 Jan;9(1):68. doi: 10.21037/atm-20-3140.
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First Report of a Patient With Natural Killer-Lymphoblastic Leukemia/Lymphoma in Korea.
Ann Lab Med. 2019 Sep;39(5):493-495. doi: 10.3343/alm.2019.39.5.493.
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Pediatr Hematol Oncol. 2011 Apr;28(3):187-93. doi: 10.3109/08880018.2010.535117. Epub 2011 Jan 27.
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Pediatric myeloid/NK cell precursor lymphoma/leukemia expressing T/NK immunophenotype markers.表达 T/NK 免疫表型标志物的小儿髓系/NK 细胞前体细胞淋巴瘤/白血病。
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