Suppr超能文献

白色血小板综合征:一种新的常染色体显性血小板疾病。

The White platelet syndrome: a new autosomal dominant platelet disorder.

作者信息

White James G, Key Nigel S, King Richard A, Vercellotti Gregory M

机构信息

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Platelets. 2004 May;15(3):173-84. doi: 10.1080/09537100410001682805.

Abstract

The present study has evaluated 46 members from four generations of a large family with mild to moderate bleeding symptoms, prolonged bleeding times and poor responses to all aggregating agents. Twenty-one members of the family had all of the abnormal structural features of the disorder brought to Minnesota in 1870 by Esther White and, therefore, referred to as the White platelet syndrome (WPS). Their platelet counts were decreased and mean platelet volumes increased. Four to 13% of their platelets contained large, fully developed Golgi complexes actively budding smooth and coated vesicles and frequently associated with centrioles. Such structures are usually present in megakaryocytes only during the major phase of granulopoiesis. As many as seven Golgi complexes and five centrioles were present in single platelets. Alpha granule formation appeared incomplete in patient platelets. The organelles were often immature in appearance and markedly decreased in number in many of their cells. As a result 30% or more of WPS platelets were "gray platelets" similar to, yet very different from the cells in patients with the gray platelet syndrome. Other abnormal features included cytoplasmic sequestration by residual dense tubular system membranes, autodigestion, larger than normal mitochondria and half normal-sized dense bodies. Thirteen of the 46 family members had a "touch" of WPS. Three to 5% of their platelets contained Golgi complexes. However, gray platelets were not present among their circulating cells. The WPS is a unique autosomal dominant condition that can be classified among the platelet granule deficiency disorders.

摘要

本研究评估了一个大家族中四代的46名成员,他们有轻度至中度出血症状、出血时间延长,且对所有聚集剂反应不佳。该家族中有21名成员具有1870年由埃丝特·怀特带到明尼苏达州的这种疾病的所有异常结构特征,因此被称为怀特血小板综合征(WPS)。他们的血小板计数降低,平均血小板体积增加。他们4%至13%的血小板含有大型、发育完全的高尔基体复合物,这些复合物活跃地产生光滑和有被小泡,并经常与中心粒相关联。这种结构通常仅在粒细胞生成的主要阶段存在于巨核细胞中。单个血小板中多达七个高尔基体复合物和五个中心粒。患者血小板中的α颗粒形成似乎不完全。这些细胞器在外观上往往不成熟,并且在许多细胞中的数量明显减少。结果,30%或更多的WPS血小板是“灰色血小板”,与灰色血小板综合征患者的细胞相似但又非常不同。其他异常特征包括被残余致密管状系统膜进行细胞质隔离、自噬、线粒体大于正常以及致密小体大小只有正常的一半。46名家族成员中有13名有轻微的WPS症状。他们3%至5%的血小板含有高尔基体复合物。然而,在他们的循环细胞中不存在灰色血小板。WPS是一种独特的常染色体显性疾病,可归类于血小板颗粒缺乏症。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验