摘要
血小板无力症是由于Ⅱb/Ⅲa数量或结构异常,导致血小板对多种诱聚剂反应不良的少见遗传病。本文报道1例遗传性血小板无力症患者洁治后出血不止的病例。
Glanzmann thrombasthenia(GT) is an inherited disease of platelet function disorders characterized by mucocutaneous bleeding due to platelets failure to aggregate in response to physiologic stimuli. GT is a rare inherited disease and caused by quantitative or qualitative deficiencies of Ⅱb/Ⅲa. A case with GT with uncontrolled gingival bleeding after scalling is reported in this paper.
作者
班建东
齐凤娜
冯向辉
侯燕
刘涛
周传奇
李军科
王宏伟
BAN Jiandong;QI Fengna;FENG Xianghui;HOU Yan;LIU Tao;ZHOU Chuanqi;LI Junke;WANG Hong-wei(Departerment of Oral Medicine of Eye Hospital of Hebei,China,Xingtai 054000;Department of Periodontology,Peking University School and Hospital of Stomatology,Beijing;Departerment of Laboratory Medicine of Eye Hospital of Hebei,Xingtai)
出处
《实用口腔医学杂志》
CAS
CSCD
北大核心
2020年第4期690-691,共2页
Journal of Practical Stomatology
基金
河北省科技厅科技支撑计划项目(编号:132777252)
河北省邢台市科技支撑计划项目(编号:2019ZC143)。
关键词
血小板无力症
牙龈出血
洁治
血小板输注
氨甲环酸
Glanzmann thrombasthenia
Gingival bleeding
Scalling
Platelet infusion
Tranexamic acid
