• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Assessment of dysplastic hematopoiesis: lessons from healthy bone marrow donors.病态造血的评估:来自健康骨髓供者的经验。
Haematologica. 2012 May;97(5):723-30. doi: 10.3324/haematol.2011.056879. Epub 2011 Dec 16.
2
De novo AML with dysplastic hematopoiesis: cytogenetic and prognostic significance.伴有发育异常造血的原发性急性髓系白血病:细胞遗传学及预后意义
Leukemia. 1996 Jun;10(6):946-51.
3
Evaluation of the dysmyelopoiesis in 336 patients with de novo acute myeloid leukemia: major importance of dysgranulopoiesis for remission and survival.336例初发急性髓系白血病患者骨髓生成异常的评估:粒细胞生成异常对缓解和生存的重要意义
Leukemia. 1992 Jun;6(6):520-5.
4
Reevaluation of reference values for bone marrow differential counts in 236 healthy bone marrow donors.236 例健康骨髓供者骨髓细胞分类计数参考值的再评估。
Ann Hematol. 2020 Dec;99(12):2723-2729. doi: 10.1007/s00277-020-04255-4. Epub 2020 Sep 15.
5
Specific Features of Interactions between Megakaryocytic and Granulocytic Hematopoiesis Lineages and Myelofibrosis during the Acute Phase of Chronic Myeloid Leukemia, Chronic Lymphocytic Leukemia, and Multiple Myeloma.巨核细胞和粒细胞造血谱系在慢性髓性白血病、慢性淋巴细胞白血病和多发性骨髓瘤急性期与骨髓纤维化之间相互作用的特定特征。
Bull Exp Biol Med. 2020 Apr;168(6):734-738. doi: 10.1007/s10517-020-04791-z. Epub 2020 Apr 25.
6
Bone marrow examination in patients with immune thrombocytopenia: is there anything different in older patients?免疫性血小板减少症患者的骨髓检查:老年患者有何不同之处?
Eur J Haematol. 2014 Aug;93(2):157-60. doi: 10.1111/ejh.12320. Epub 2014 Apr 9.
7
Megakaryopoiesis and myelofibrosis in chronic myeloid leukemia after allogeneic bone marrow transplantation: an immunohistochemical study of 127 patients.异基因骨髓移植后慢性髓性白血病的巨核细胞生成与骨髓纤维化:127例患者的免疫组织化学研究
Mod Pathol. 2001 Feb;14(2):129-38. doi: 10.1038/modpathol.3880269.
8
Myelopoiesis and myeloproliferative disorders.髓系造血与骨髓增殖性疾病
Vet Clin North Am Small Anim Pract. 1996 Sep;26(5):1023-42. doi: 10.1016/s0195-5616(96)50054-9.
9
Influence of T lymphocytes on hematopoiesis in a patient with T cell hypoplasia.T淋巴细胞对一名T细胞发育不全患者造血作用的影响。
Am J Hematol. 1988 Feb;27(2):118-24. doi: 10.1002/ajh.2830270210.
10
Treatment of chronic myelogenous leukemia with the tyrosine kinase inhibitor STI571 results in marked regression of bone marrow fibrosis.使用酪氨酸激酶抑制剂STI571治疗慢性粒细胞白血病可导致骨髓纤维化显著消退。
Blood. 2002 Jan 1;99(1):381-3. doi: 10.1182/blood.v99.1.381.

引用本文的文献

1
AI-based detection of neutrophil dysplasia: an accessible and sensitive model for MDS diagnosis from peripheral blood.基于人工智能的中性粒细胞发育异常检测:一种用于从外周血诊断骨髓增生异常综合征的便捷且灵敏的模型。
Ann Hematol. 2025 Aug 19. doi: 10.1007/s00277-025-06533-5.
2
Monitoring clonal burden as an alternative to blast count for myelodysplastic neoplasm treatment response.监测克隆负荷作为骨髓增生异常综合征治疗反应中原始细胞计数的替代指标。
Leukemia. 2025 Jan;39(1):166-177. doi: 10.1038/s41375-024-02426-0. Epub 2024 Oct 4.
3
Integrating AI and ML in Myelodysplastic Syndrome Diagnosis: State-of-the-Art and Future Prospects.将人工智能和机器学习整合到骨髓增生异常综合征诊断中:现状与未来展望。
Cancers (Basel). 2023 Dec 22;16(1):65. doi: 10.3390/cancers16010065.
4
Utility of targeted gene sequencing to differentiate myeloid malignancies from other cytopenic conditions.靶向基因测序在鉴别髓系恶性肿瘤与其他血细胞减少症中的作用。
Blood Adv. 2023 Jul 25;7(14):3749-3759. doi: 10.1182/bloodadvances.2022008578.
5
Incidence of myeloid neoplasms in Spain (2002-2013): a population-based study of the Spanish network of cancer registries.西班牙髓系肿瘤发病率(2002-2013 年):西班牙癌症登记处网络的一项基于人群的研究。
Sci Rep. 2022 Jan 10;12(1):323. doi: 10.1038/s41598-021-03734-6.
6
When are idiopathic and clonal cytopenias of unknown significance (ICUS or CCUS)?特发性和克隆性血细胞减少症的不明意义(ICUS 或 CCUS)是什么时候?
Hematology Am Soc Hematol Educ Program. 2021 Dec 10;2021(1):399-404. doi: 10.1182/hematology.2021000272.
7
Myelodysplastic syndrome in a 30-year-old man with coronavirus disease 2019 (COVID-19): a diagnostic challenge.一名患有2019冠状病毒病(COVID-19)的30岁男性的骨髓增生异常综合征:一项诊断挑战。
Autops Case Rep. 2021 Apr 20;11:e2021274. doi: 10.4322/acr.2021.274.
8
Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes.临床综合基因组特征分析在低细胞性骨髓衰竭综合征患者诊断分类中的应用
Haematologica. 2021 Jan 1;106(1):64-73. doi: 10.3324/haematol.2019.237693.
9
The diagnostic utility of targeted gene panel sequencing in discriminating etiologies of cytopenia.靶向基因panel 测序在鉴别血细胞减少病因中的诊断效用。
Am J Hematol. 2019 Oct;94(10):1141-1148. doi: 10.1002/ajh.25592. Epub 2019 Aug 7.
10
Eltrombopag in Immune Thrombocytopenia, Aplastic Anemia, and Myelodysplastic Syndrome: From Megakaryopoiesis to Immunomodulation.依鲁替尼在免疫性血小板减少症、再生障碍性贫血和骨髓增生异常综合征中的作用:从巨核细胞生成到免疫调节。
Drugs. 2019 Aug;79(12):1305-1319. doi: 10.1007/s40265-019-01159-0.

本文引用的文献

1
The epidemiology of myelodysplastic syndromes.骨髓增生异常综合征的流行病学。
Hematol Oncol Clin North Am. 2010 Apr;24(2):287-94. doi: 10.1016/j.hoc.2010.02.011.
2
Smoking and alcohol intake as risk factors for myelodysplastic syndromes (MDS).吸烟和饮酒作为骨髓增生异常综合征(MDS)的危险因素。
Leuk Res. 2010 Jan;34(1):1-5. doi: 10.1016/j.leukres.2009.08.006. Epub 2009 Sep 10.
3
Minimal diagnostic criteria for myelodysplastic syndromes and separation from ICUS and IDUS: update and open questions.骨髓增生异常综合征的最低诊断标准与 ICUS 和 IDUS 的分离:更新和未解决的问题。
Eur J Clin Invest. 2009 Jul;39(7):548-53. doi: 10.1111/j.1365-2362.2009.02151.x. Epub 2009 May 6.
4
Obesity, lifestyle factors, and risk of myelodysplastic syndromes in a large US cohort.美国一个大型队列中肥胖、生活方式因素与骨髓增生异常综合征风险
Am J Epidemiol. 2009 Jun 15;169(12):1492-9. doi: 10.1093/aje/kwp074. Epub 2009 Apr 24.
5
Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts.骨髓增生异常综合征的诊断与分类:骨髓增生异常综合征形态学国际工作组(IWGM-MDS)关于原始粒细胞和环形铁粒幼细胞定义及计数的共识建议
Haematologica. 2008 Nov;93(11):1712-7. doi: 10.3324/haematol.13405. Epub 2008 Oct 6.
6
ICSH guidelines for the standardization of bone marrow specimens and reports.国际血液学标准化委员会(ICSH)关于骨髓标本及报告标准化的指南。
Int J Lab Hematol. 2008 Oct;30(5):349-64. doi: 10.1111/j.1751-553X.2008.01100.x.
7
Epidemiology of myelodysplastic syndromes and chronic myeloproliferative disorders in the United States, 2001-2004, using data from the NAACCR and SEER programs.利用北美癌症登记协会(NAACCR)和监测、流行病学与最终结果(SEER)项目的数据,对2001 - 2004年美国骨髓增生异常综合征和慢性骨髓增殖性疾病的流行病学进行研究。
Blood. 2008 Jul 1;112(1):45-52. doi: 10.1182/blood-2008-01-134858. Epub 2008 Apr 28.
8
Epidemiology of myelodysplastic syndromes.骨髓增生异常综合征的流行病学
Semin Hematol. 2008 Jan;45(1):8-13. doi: 10.1053/j.seminhematol.2007.10.003.
9
A new disease categorization of low-grade myelodysplastic syndromes based on the expression of cytopenia and dysplasia in one versus more than one lineage improves on the WHO classification.一种基于一个与多个谱系中血细胞减少和发育异常的表达对低级别骨髓增生异常综合征进行的新疾病分类,比世界卫生组织的分类有所改进。
Leukemia. 2007 Apr;21(4):668-77. doi: 10.1038/sj.leu.2404564. Epub 2007 Feb 15.
10
Improvement of criteria for refractory cytopenia with multilineage dysplasia according to the WHO classification based on prognostic significance of morphological features in patients with refractory anemia according to the FAB classification.根据FAB分类中难治性贫血患者形态学特征的预后意义,依据世界卫生组织分类改进伴有多系发育异常的难治性血细胞减少症的标准。
Leukemia. 2007 Apr;21(4):678-86. doi: 10.1038/sj.leu.2404571. Epub 2007 Feb 1.

病态造血的评估:来自健康骨髓供者的经验。

Assessment of dysplastic hematopoiesis: lessons from healthy bone marrow donors.

机构信息

Medizinische Klinik und Poliklinik I, Universitätsklinikum Dresden, Fetscherstraße 74, 01307 Dresden, Germany.

出版信息

Haematologica. 2012 May;97(5):723-30. doi: 10.3324/haematol.2011.056879. Epub 2011 Dec 16.

DOI:10.3324/haematol.2011.056879
PMID:22180437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3342975/
Abstract

BACKGROUND

According to WHO 2008 guidelines, the required percentage of cells manifesting dysplasia in the bone marrow to qualify as significant is 10% or over in one or more hematopoietic cell lineages, but this threshold is controversial. No 'normal' values have been established. Therefore, we investigated dyshematopoiesis in bone marrow aspirate squash preparations of 120 healthy bone marrow donors.

DESIGN AND METHODS

Bone marrow squash slides of 120 healthy unrelated bone marrow donors were examined independently by 4 experienced morphologists. Samples were taken from the first aspiration during the harvest. Bone marrow preparation and assessment were performed according to WHO recommendations and ICSH guidelines.

RESULTS

More than 10% dysmyelopoiesis could be detected in 46% of bone marrow aspirate squash preparations with 26% in 2 or more cell lineages and 7% in 3 cell lineages in healthy bone marrow donors. Donors under the age of 30 years exhibited more dysgranulopoietic changes and dysmegakaryopoietic changes (P<0.001) compared to the older donors. Female donors showed more dysgranulopoietic changes than male donors (P = 0.025). The concordance rate between the 4 investigators was modest in dysgranulopoiesis but poor in dyserythropoiesis and dysmegakaryopoiesis.

CONCLUSIONS

The poor reliability of the 10% cut off was partly related to the proximity of the current criteria to the observed cut-off mean values of the normal population. These findings question the current WHO threshold of the 10% or over necessary for the percentage of cells manifesting dysplasia to be considered significant, and suggest that either a higher threshold would be more appropriate or different thresholds should be set for each lineage.

摘要

背景

根据世卫组织 2008 年的指南,在一个或多个造血细胞谱系中,骨髓中表现出发育不良的细胞比例达到 10%或以上,即可被认为具有显著意义,但这一门槛存在争议。目前尚未确定“正常”值。因此,我们调查了 120 名健康骨髓供者的骨髓抽吸液涂片的血液发育不良情况。

设计和方法

由 4 位经验丰富的形态学家独立检查 120 名健康无关骨髓供者的骨髓抽吸液涂片。样本取自采集过程中的第一次抽吸。骨髓制备和评估按照世卫组织的建议和国际血液学标准化委员会的指南进行。

结果

在 120 名健康骨髓供者中,超过 10%的骨髓抽吸液涂片可检测到发育不良,其中 26%的患者有 2 种以上细胞谱系的发育不良,7%的患者有 3 种细胞谱系的发育不良。年龄小于 30 岁的供者比年龄较大的供者表现出更多的粒系发育不良和巨核细胞发育不良改变(P<0.001)。女性供者比男性供者表现出更多的粒系发育不良改变(P=0.025)。在粒系发育不良方面,4 位研究者之间的一致性率适中,但在红系发育不良和巨核细胞发育不良方面的一致性率较差。

结论

10%界限的可靠性较差,部分原因是目前的标准与正常人群观察到的界限平均值接近。这些发现对当前世卫组织规定的 10%或以上的细胞比例作为显著发育不良的标准提出了质疑,并表明需要设定更高的阈值,或者为每个谱系设定不同的阈值。