骨髓增生异常综合征中的17号等臂染色体：一种独特实体的标志物。 - Suppr

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Isochromosome 17q in MDS: a marker of a distinct entity.

作者信息

Pinheiro Ronald Feitosa, Chauffaille Maria de Lourdes L F, Silva Maria Regina Régis

出版信息

Cancer Genet Cytogenet. 2006 Apr 15;166(2):189-90. doi: 10.1016/j.cancergencyto.2005.10.004.

DOI:10.1016/j.cancergencyto.2005.10.004

PMID:16631479

Abstract

摘要

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Isochromosome 17q in MDS: a marker of a distinct entity.骨髓增生异常综合征中的17号等臂染色体：一种独特实体的标志物。

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Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.伴有17号染色体长臂等臂染色体和14号染色体三体的白血病转化的骨髓增生异常综合征患者

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[Clinical and experimental study of two cases of myelodysplastic syndromes with double isochromosome 20q- anomaly].两例伴有双等臂20号染色体异常的骨髓增生异常综合征的临床与实验研究

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A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies.对骨髓增生异常综合征中发现的两种截然不同的复发性20号等臂染色体的比较表明，20号染色体长臂近端的保留是髓系恶性肿瘤的一个重要因素。

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Isolated 5p isochromosome in myelodysplastic syndrome: report of the first case.骨髓增生异常综合征中孤立的5号染色体等臂染色体：首例报告

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Isolated isochromosome 17q in myelodysplastic syndromes with pure red cell aplasia and basophilia.伴有纯红细胞再生障碍和嗜碱性粒细胞增多的骨髓增生异常综合征中的孤立性17号等臂染色体。

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Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53.孤立性 17q 等臂染色体髓系肿瘤是一种临床病理实体，与骨髓增生异常/骨髓增殖性特征、白血病转化风险高和野生型 TP53 相关。

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Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies.

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Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course.孤立性17号染色体长臂等臂染色体：一种具有侵袭性临床病程的独特类型的混合性骨髓增殖性疾病/骨髓增生异常综合征。

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Case report of isochromosome 17q in acute myeloid leukemia with myelodysplasia-related changes after treatment with a hypomethylating agent.急性髓系白血病伴骨髓增生异常相关改变患者经去甲基化药物治疗后出现17号染色体等臂染色体的病例报告。

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Changing the frequency and spectra of chromosomal aberrations in Korean patients with acute leukemia in a tertiary care hospital.三级护理医院中韩国急性白血病患者染色体畸变频率和谱的变化

Blood Res. 2020 Dec 31;55(4):225-245. doi: 10.5045/br.2020.2020255.

The prognostic significance of chromosome 17 abnormalities in patients with myelodysplastic syndrome treated with 5-azacytidine: Results from the Hellenic 5-azacytidine registry.5- 氮杂胞苷治疗骨髓增生异常综合征患者中 17 号染色体异常的预后意义：来自希腊 5- 氮杂胞苷登记处的结果。

Cancer Med. 2019 May;8(5):2056-2063. doi: 10.1002/cam4.2090. Epub 2019 Mar 21.

Isochromosome 17q; A Novel Finding in Myeloid Sarcoma.17号染色体等臂染色体；髓系肉瘤中的新发现。

J Clin Exp Hematop. 2016;56(2):130-134. doi: 10.3960/jslrt.56.130.

The landscape of myeloid neoplasms with isochromosome 17q discloses a specific mutation profile and is characterized by an accumulation of prognostically adverse molecular markers.伴有17号染色体长臂等臂染色体的髓系肿瘤格局揭示了一种特定的突变谱，并以预后不良分子标志物的积累为特征。

Leukemia. 2016 Jul;30(7):1624-7. doi: 10.1038/leu.2016.21. Epub 2016 Feb 9.

Spectra of chromosomal aberrations in 325 leukemia patients and implications for the development of new molecular detection systems.325 例白血病患者染色体畸变的频谱及其对新的分子检测系统发展的意义。

J Korean Med Sci. 2011 Jul;26(7):886-92. doi: 10.3346/jkms.2011.26.7.886. Epub 2011 Jun 20.

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