Thrombotic microangiopathy during pregnancy

被引:16
作者
Vahed, Sepideh Zununi [1 ]
Saadat, Yalda Rahbar [1 ]
Ardalan, Mohammadreza [1 ]
机构
[1] Tabriz Univ Med Sci, Kidney Res Ctr, Tabriz, Iran
关键词
Purpura; thrombotic thrombocytopenic; Pre-eclampsia; Atypical hemolytic uremic syndrome; Pregnancy; Microangiopathy; HEMOLYTIC-UREMIC SYNDROME; H-RELATED PROTEIN-1; COMPLEMENT FACTOR-H; THROMBOCYTOPENIC PURPURA; HELLP-SYNDROME; ALTERNATIVE PATHWAY; ADAMTS13; DEFICIENCY; SOLUBLE ENDOGLIN; DISEASE; PREECLAMPSIA;
D O I
10.1016/j.mvr.2021.104226
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Pregnancy is a high-risk time for the development of different kinds of thrombotic microangiopathy (TMA). Three major syndromes including TTP (thrombotic thrombocytopenic purpura), PE/HELLP (preeclampsia/hemolysis, elevated liver function tests, low platelets), and aHUS (atypical hemolytic- uremic syndrome) should be sought in pregnancy-TMA. These severe disorders share multiple clinical features and overlaps and even the coexistence of more than one pathologic mechanism. Each of these disorders finally ends in endothelial damage and fibrin thrombi formation within the microcirculation that fragments RBCs (schystocytes), aggregates platelets, and creates ischemic injury in the targeted organs i.e.; kidney and brain. Although the mechanisms of these severe disorders have been revealed, pregnancy-related TMA still interfaces with diagnostic and therapeutic challenges. Here, we highlight the current knowledge of diagnosis and management of these complications during pregnancy.
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页数:6
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