• 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

地中海贫血中血小板活化的形态学评估。

Morphological assessment of platelet activation in thalassemia.

作者信息

Bunyaratvej A, Komanasin N, Sriurairatana S, Fucharoen S

机构信息

Department of Pathology, Faculty of Medicine, Ramathibodi Hospital, Thailand.

出版信息

Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:60-4.

PMID:1298995
Abstract

Platelets from patients with beta-thalassemia/hemoglobin E, both splenectomized and nonsplenectomized cases, were examined in comparison to those from normal subjects by scanning electron microscopy. In normal subjects, the majority of platelets were discoid (mean +/- SD, 81.0 +/- 3.9%) with 17.3 +/- 3.5% type I spherical shapes (platelet with long axis/short axis greater than 1.1) and 1.3 +/- 1.0% type II (long axis/short axis = 1.0-1.1). The thalassemic patients had significant lower percentage of discoid platelets (60.9 +/- 8.1% in nonsplenectomized patients, 49.2 +/- 9.1% in splenectomized patients) and increase in spherical platelets (nonsplenectomized patients had 36.6 +/- 8.3% type I, 4.0 +/- 1.5% type II; splenectomized patients had 43.4 +/- 7.9% type I, 8.3 +/- 4.5% type II). Study of platelet reversibility from pseudopods to smooth surface showed that thalassemic platelets had poorer reversibility than normal platelets. Splenectomized patients had lower platelet pseudopod reversibility than nonsplenectomized cases. The shape changes and impaired reversibility of platelet pseudopods may be associated with the high tendency of pulmonary thrombus in beta-thal/HbE patients.

摘要

通过扫描电子显微镜,对β地中海贫血/血红蛋白E患者(包括脾切除和未脾切除病例)的血小板与正常受试者的血小板进行了检查。在正常受试者中,大多数血小板呈盘状(平均值±标准差,81.0±3.9%),17.3±3.5%为I型球形(长轴/短轴大于1.1的血小板),1.3±1.0%为II型(长轴/短轴=1.0 - 1.1)。地中海贫血患者的盘状血小板百分比显著降低(未脾切除患者为60.9±8.1%,脾切除患者为49.2±9.1%),球形血小板增加(未脾切除患者有36.6±8.3%的I型,4.0±1.5%的II型;脾切除患者有43.4±7.9%的I型,8.3±4.5%的II型)。对血小板从伪足到光滑表面的可逆性研究表明,地中海贫血患者的血小板可逆性比正常血小板差。脾切除患者的血小板伪足可逆性低于未脾切除病例。血小板伪足的形状变化和可逆性受损可能与β地中海贫血/血红蛋白E患者肺血栓形成的高倾向有关。

相似文献

1
Morphological assessment of platelet activation in thalassemia.地中海贫血中血小板活化的形态学评估。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:60-4.
2
Differentiation of platelets from red cell fragments using laser technology: comparison between splenectomized and nonsplenectomized thalassemic patients.利用激光技术区分血小板与红细胞碎片:脾切除和未脾切除的地中海贫血患者的比较
Southeast Asian J Trop Med Public Health. 1993;24 Suppl 1:250-2.
3
Increase in spontaneous platelet aggregation in beta-thalassemia/hemoglobin E disease: a consequence of splenectomy.β地中海贫血/血红蛋白E病患者自发性血小板聚集增加:脾切除术后的结果
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:36-41.
4
Spontaneous platelet aggregation in thalassemic children and adolescents.地中海贫血儿童和青少年的自发性血小板聚集
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:42-6.
5
Platelet aggregation and activation in thalassemia major patients in Indonesia.印度尼西亚重型地中海贫血患者的血小板聚集与活化
Clin Appl Thromb Hemost. 2008 Jul;14(3):346-51. doi: 10.1177/1076029607306397. Epub 2007 Dec 26.
6
Detection of PF3 availability in whole blood from volunteers and beta-thalassemia/HbE patients: a promising method for prediction of thrombotic tendency.检测志愿者及β地中海贫血/HbE患者全血中PF3的可用性:一种预测血栓形成倾向的有前景的方法。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:52-9.
7
Interaction between endothelial cells and thalassemic red cells in vitro.体外内皮细胞与地中海贫血红细胞之间的相互作用。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:101-4.
8
Increased platelet adhesion under flow conditions is induced by both thalassemic platelets and red blood cells.在流动条件下,地中海贫血患者的血小板和红细胞均会导致血小板黏附增加。
Thromb Haemost. 2008 Nov;100(5):864-70.
9
Protein C and protein S deficiency in thalassemic patients.地中海贫血患者的蛋白C和蛋白S缺乏症
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:65-73.
10
Significance of blood coagulation and platelet profiles in relation to pulmonary thrombosis in beta-thalassemia/Hb E.β地中海贫血/Hb E患者血液凝固和血小板指标与肺血栓形成的关系
Southeast Asian J Trop Med Public Health. 1994 Sep;25(3):449-56.

引用本文的文献

1
In vivo platelet activation and hyperaggregation in hemoglobin E/beta-thalassemia: a consequence of splenectomy.血红蛋白E/β地中海贫血患者体内的血小板激活与高聚集:脾切除的后果
Int J Hematol. 2003 Apr;77(3):299-303. doi: 10.1007/BF02983790.