• 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

骨髓增生异常综合征的FAB分类:优点与争议

FAB classification of myelodysplastic syndromes: merits and controversies.

作者信息

Verhoef G E, Pittaluga S, De Wolf-Peeters C, Boogaerts M A

机构信息

Department of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.

出版信息

Ann Hematol. 1995 Jul;71(1):3-11. doi: 10.1007/BF01696227.

DOI:10.1007/BF01696227
PMID:7632816
Abstract

Guidelines for the definition and diagnosis of myelodysplasia were set out by the French-American-British Cooperative group (FAB), and the resulting framework has greatly helped the now very large number of workers in many scientific disciplines who are actively investigating the myelodysplastic syndromes (MDS). Most patients with MDS can be readily classified into clinically relevant subgroups by correlation of clinical findings with the findings from well-prepared peripheral blood and bone marrow specimens. However, there are several areas where the standard morphological features are insensitive, but integration of these parameters with histology and cytogenetic and molecular techniques may help us in understanding this fascinating disease.

摘要

法国 - 美国 - 英国合作组(FAB)制定了骨髓发育异常的定义和诊断指南,由此形成的框架极大地帮助了众多来自许多科学学科、正在积极研究骨髓增生异常综合征(MDS)的科研人员。通过将临床发现与精心制备的外周血和骨髓标本的检查结果相关联,大多数MDS患者能够很容易地被归入具有临床相关性的亚组。然而,在几个方面,标准形态学特征并不敏感,但将这些参数与组织学、细胞遗传学和分子技术相结合,可能有助于我们理解这种引人入胜的疾病。

相似文献

1
FAB classification of myelodysplastic syndromes: merits and controversies.骨髓增生异常综合征的FAB分类:优点与争议
Ann Hematol. 1995 Jul;71(1):3-11. doi: 10.1007/BF01696227.
2
Diagnosis, classification, and cytogenetics of myelodysplastic syndromes.骨髓增生异常综合征的诊断、分类及细胞遗传学
Haematologica. 1998 Mar;83(3):258-75.
3
The classification of MDS: from FAB to WHO and beyond.MDS 的分类:从 FAB 到 WHO 及其他。
Leuk Res. 2012 Dec;36(12):1453-8. doi: 10.1016/j.leukres.2012.08.008. Epub 2012 Aug 30.
4
Prognostic relevance of morphological classification models for myelodysplastic syndromes in an era of the revised International Prognostic Scoring System.在修订的国际预后评分系统时代,骨髓增生异常综合征形态学分类模型的预后相关性。
Eur J Cancer. 2016 Mar;56:10-20. doi: 10.1016/j.ejca.2015.12.004. Epub 2016 Jan 19.
5
A comparative review of classification systems in myelodysplastic syndromes (MDS).骨髓增生异常综合征(MDS)分类系统的比较综述。
Semin Oncol. 2005 Aug;32(4 Suppl 5):S3-10. doi: 10.1053/j.seminoncol.2005.06.021.
6
Validation of the WHO proposals for a new classification of primary myelodysplastic syndromes: a retrospective analysis of 1600 patients.世界卫生组织原发性骨髓增生异常综合征新分类建议的验证:对1600例患者的回顾性分析
Leuk Res. 2000 Dec;24(12):983-92. doi: 10.1016/s0145-2126(00)00088-6.
7
The myelodysplastic syndromes: diagnosis, molecular biology and risk assessment.骨髓增生异常综合征:诊断、分子生物学及风险评估
Hematology. 2005;10 Suppl 1:258-69. doi: 10.1080/10245330512331390311.
8
[Myelodysplastic syndromes: preleukemic syndromes].[骨髓增生异常综合征:白血病前期综合征]
Rev Med Liege. 1998 Jun;53(6):357-62.
9
Histopathology of myelodysplastic syndromes. The FAB classification (proposals) applied to bone marrow biopsy.骨髓增生异常综合征的组织病理学。应用于骨髓活检的FAB分类(建议)。
Am J Clin Pathol. 1987 Feb;87(2):180-6. doi: 10.1093/ajcp/87.2.180.
10
Hematopathological concepts and controversies in the diagnosis and classification of myelodysplastic syndromes.骨髓增生异常综合征诊断与分类中的血液病理学概念及争议
Hematology Am Soc Hematol Educ Program. 2006:199-204. doi: 10.1182/asheducation-2006.1.199.

本文引用的文献

1
Myeloid but not lymphoid cells carry the 5q deletion: polymerase chain reaction analysis of loss of heterozygosity using mini-repeat sequences on highly purified cell fractions.髓系而非淋巴系细胞存在5q缺失:利用高度纯化细胞组分上的微重复序列对杂合性缺失进行聚合酶链反应分析。
Blood. 1993 Apr 1;81(7):1849-54.
2
High Ia (HLA-DR) and low CD11b (Mo1) expression may predict early conversion to leukemia in myelodysplastic syndromes.高Ia(HLA - DR)和低CD11b(Mo1)表达可能预示骨髓增生异常综合征早期转化为白血病。
Am J Hematol. 1993 Jul;43(3):165-71. doi: 10.1002/ajh.2830430302.
3
In situ hybridization on May-Grünwald Giemsa-stained bone marrow and blood smears of patients with hematologic disorders allows detection of cell-lineage-specific cytogenetic abnormalities.
对血液系统疾病患者的May-Grünwald Giemsa染色骨髓涂片和血涂片进行原位杂交,可检测细胞系特异性细胞遗传学异常。
Blood. 1993 Aug 1;82(3):884-8.
4
The prognostic significance of auer rods in myelodysplasia.奥厄小体在骨髓增生异常综合征中的预后意义。
Br J Haematol. 1993 Sep;85(1):67-76. doi: 10.1111/j.1365-2141.1993.tb08647.x.
5
Myelodysplastic syndrome evolving into a myeloproliferative disorder: one disease or two?骨髓增生异常综合征演变为骨髓增殖性疾病:一种疾病还是两种?
Leukemia. 1994 Apr;8(4):714-5.
6
Clonality in myelodysplastic syndromes: demonstration of pluripotent stem cell origin using X-linked restriction fragment length polymorphisms.骨髓增生异常综合征中的克隆性:利用X连锁限制性片段长度多态性证明多能干细胞起源
Br J Haematol. 1993 Apr;83(4):589-94. doi: 10.1111/j.1365-2141.1993.tb04695.x.
7
Detection of minimal residual disease state in chronic myelogenous leukemia patients using fluorescence in situ hybridization.利用荧光原位杂交技术检测慢性粒细胞白血病患者的微小残留病状态
Cancer Genet Cytogenet. 1994 Aug;76(1):59-64. doi: 10.1016/0165-4608(94)90073-6.
8
The chronic myeloid leukaemias: guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British Cooperative Leukaemia Group.慢性髓细胞白血病:鉴别慢性粒细胞白血病、非典型慢性髓细胞白血病和慢性粒-单核细胞白血病的指南。法美英协作白血病组的建议
Br J Haematol. 1994 Aug;87(4):746-54. doi: 10.1111/j.1365-2141.1994.tb06734.x.
9
Prognostic implications of bone marrow culturing in myelodysplastic syndrome: a retrospective analysis.骨髓培养在骨髓增生异常综合征中的预后意义:一项回顾性分析。
Leuk Lymphoma. 1994 Jun;14(1-2):111-20. doi: 10.3109/10428199409049656.
10
Point mutations of the N-ras gene in the blood plasma DNA of patients with myelodysplastic syndrome or acute myelogenous leukaemia.骨髓增生异常综合征或急性髓性白血病患者血浆DNA中N-ras基因的点突变
Br J Haematol. 1994 Apr;86(4):774-9. doi: 10.1111/j.1365-2141.1994.tb04828.x.