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[Acute promyelocytic leukemia with PML cryptic breakpoint t (15; 17) (q22; q21) negative: a case report and literatures review].

作者信息

Wu C Y, Li Y L, Dong X Y, Zhang L, Shang B J, Cheng W, Huang Z F, Zhu Z M

机构信息

Institute of Hematology, Henan Provincial People's Hospital; Henan Key Laboratory for Hematopathology; Henan Key Laboratory of Stem Cell Differentiation and Modification; Zhengzhou University People's Hospital, Henan University People's Hospital, Zhengzhou, Henan 450003, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2021 Jan 14;42(1):74-77. doi: 10.3760/cma.j.issn.0253-2727.2021.01.014.

DOI:10.3760/cma.j.issn.0253-2727.2021.01.014
PMID:33677873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7957259/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/25403a481d78/cjh-42-01-074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/9fa591e51622/cjh-42-01-074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/e6c38121b097/cjh-42-01-074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/c14d46f84469/cjh-42-01-074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/25403a481d78/cjh-42-01-074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/9fa591e51622/cjh-42-01-074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/e6c38121b097/cjh-42-01-074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/c14d46f84469/cjh-42-01-074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a57/7957259/25403a481d78/cjh-42-01-074-g004.jpg

相似文献

1
[Acute promyelocytic leukemia with PML cryptic breakpoint t (15; 17) (q22; q21) negative: a case report and literatures review].[隐匿性PML断点t(15;17)(q22;q21)阴性的急性早幼粒细胞白血病:1例报告及文献复习]
Zhonghua Xue Ye Xue Za Zhi. 2021 Jan 14;42(1):74-77. doi: 10.3760/cma.j.issn.0253-2727.2021.01.014.
2
A PML/RARA chimeric gene on chromosome 2 in a patient with acute promyelocytic leukemia (M3) associated with a new variant translocation: t(2;15;17)(q21;q22;q21).一名急性早幼粒细胞白血病(M3)患者2号染色体上存在PML/RARA嵌合基因,伴有新的变异易位:t(2;15;17)(q21;q22;q21) 。
Cancer Genet Cytogenet. 2000 Jul 1;120(1):80-2. doi: 10.1016/s0165-4608(99)00238-1.
3
Translocation (15;17)(q22;q21) not associated with acute promyelocytic leukemia and negative for PML/RARa rearrangement.
Haematologica. 2000 Jul;85(7):768-9.
4
Acute promyelocytic leukaemia (APML) with cryptic PML-RARA fusion has a clinical course comparable to classical APML with t(15;17)(q24.1;q21.2) translocation.伴有隐匿性PML-RARA融合的急性早幼粒细胞白血病(APML)的临床病程与伴有t(15;17)(q24.1;q21.2)易位的经典APML相当。
Br J Haematol. 2019 Jul;186(1):155-157. doi: 10.1111/bjh.15738. Epub 2018 Dec 26.
5
Molecular analysis of simple variant translocations in acute promyelocytic leukemia.急性早幼粒细胞白血病中简单变异易位的分子分析
Genes Chromosomes Cancer. 1994 Apr;9(4):234-43. doi: 10.1002/gcc.2870090403.
6
A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia.一名急性早幼粒细胞白血病患者中掩盖了变异型t(15;17)(q22;q21)的t(17;20)(q21;q12) 。
Cancer Genet Cytogenet. 2006 Jul 1;168(1):73-6. doi: 10.1016/j.cancergencyto.2005.12.014.
7
Characterization of cryptic rearrangements and variant translocations in acute promyelocytic leukemia.急性早幼粒细胞白血病中隐匿重排和变异易位的特征分析
Blood. 1997 Dec 15;90(12):4876-85.
8
A PML/RARA chimeric gene on chromosome 12 in a patient with acute promyelocytic leukemia (M4) associated with a new variant translocation: t(12;15;17)(q24;q24;q11).患者患有急性早幼粒细胞白血病(M4),伴有新的变异易位:t(12;15;17)(q24;q24;q11),在 12 号染色体上存在 PML/RARA 嵌合基因。
Med Oncol. 2013 Mar;30(1):409. doi: 10.1007/s12032-012-0409-3. Epub 2013 Jan 6.
9
Identification of a new cryptic PML-RARα fusion gene without t(15;17) and biallelic CEBPA mutation in a case of acute promyelocytic leukemia: a case detected only by RT-PCR but not cytogenetics and FISH.在一个急性早幼粒细胞白血病病例中发现了一个新的隐匿性 PML-RARα 融合基因,无 t(15;17)和双等位 CEBPA 突变:该病例仅通过 RT-PCR 而非细胞遗传学和 FISH 检测到。
Cancer Biol Ther. 2020 Apr 2;21(4):309-314. doi: 10.1080/15384047.2019.1702398. Epub 2020 Jan 20.
10
A new variant t(6;15;17)(q25;q22;q21) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation.急性早幼粒细胞白血病中的一种新的变异型t(6;15;17)(q25;q22;q21):荧光原位杂交确认
Cancer Genet Cytogenet. 2005 May;159(1):69-73. doi: 10.1016/j.cancergencyto.2004.09.013.

本文引用的文献

1
Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single Fusion Gene.急性早幼粒细胞白血病:围绕单个融合基因的一系列分子事件
Cancers (Basel). 2020 Mar 8;12(3):624. doi: 10.3390/cancers12030624.
2
Outcomes in Adult Acute Promyelocytic Leukemia: A Decade Experience.成人急性早幼粒细胞白血病的疗效:十年经验。
Clin Lymphoma Myeloma Leuk. 2020 Apr;20(4):e158-e164. doi: 10.1016/j.clml.2019.12.011. Epub 2019 Dec 24.
3
Identification of a new cryptic PML-RARα fusion gene without t(15;17) and biallelic CEBPA mutation in a case of acute promyelocytic leukemia: a case detected only by RT-PCR but not cytogenetics and FISH.
在一个急性早幼粒细胞白血病病例中发现了一个新的隐匿性 PML-RARα 融合基因,无 t(15;17)和双等位 CEBPA 突变:该病例仅通过 RT-PCR 而非细胞遗传学和 FISH 检测到。
Cancer Biol Ther. 2020 Apr 2;21(4):309-314. doi: 10.1080/15384047.2019.1702398. Epub 2020 Jan 20.
4
Mutational landscape of patients with acute promyelocytic leukemia at diagnosis and relapse.初诊和复发急性早幼粒细胞白血病患者的突变图谱。
Am J Hematol. 2019 Oct;94(10):1091-1097. doi: 10.1002/ajh.25573. Epub 2019 Jul 23.
5
A novel NPM1-RARG-NPM1 chimeric fusion in acute myeloid leukaemia resembling acute promyelocytic leukaemia but resistant to all-trans retinoic acid and arsenic trioxide.一种新型的 NPM1-RARG-NPM1 嵌合融合在急性髓系白血病中类似于急性早幼粒细胞白血病,但对全反式维甲酸和三氧化二砷耐药。
Br J Cancer. 2019 May;120(11):1023-1025. doi: 10.1038/s41416-019-0456-z. Epub 2019 Apr 18.
6
Molecular landscape of acute promyelocytic leukemia at diagnosis and relapse.初诊和复发时急性早幼粒细胞白血病的分子图谱
Haematologica. 2017 Jun;102(6):e222-e224. doi: 10.3324/haematol.2016.162206. Epub 2017 Mar 24.
7
The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.2016 年版世界卫生组织髓系肿瘤和急性白血病分类。
Blood. 2016 May 19;127(20):2391-405. doi: 10.1182/blood-2016-03-643544. Epub 2016 Apr 11.
8
GTF2I-RARA is a novel fusion transcript in a t(7;17) variant of acute promyelocytic leukaemia with clinical resistance to retinoic acid.GTF2I-RARA是急性早幼粒细胞白血病t(7;17)变异型中的一种新型融合转录本,对维甲酸具有临床耐药性。
Br J Haematol. 2015 Mar;168(6):904-8. doi: 10.1111/bjh.13157. Epub 2014 Oct 4.
9
OBFC2A/RARA: a novel fusion gene in variant acute promyelocytic leukemia.OBFC2A/RARA:变异型急性早幼粒细胞白血病的一个新融合基因。
Blood. 2013 Feb 21;121(8):1432-5. doi: 10.1182/blood-2012-04-423129. Epub 2013 Jan 3.
10
The PRKAR1A gene is fused to RARA in a new variant acute promyelocytic leukemia.在一种新的变异型急性早幼粒细胞白血病中,PRKAR1A基因与RARA融合。
Blood. 2007 Dec 1;110(12):4073-6. doi: 10.1182/blood-2007-06-095554. Epub 2007 Aug 21.