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Clinical case of thrombotic microangiopathy in obstetric practice

摘要

Trombotic microangiopathy is heterogeneous group of the diseases united by a community of a histological and clinical implications at difference of pathogenetic mechanisms, presents clinical-morphological syndrome characterizing a lesion of vessels of a microcirculatory channel. Currently thrombotic microangiopathy include thrombotic thrombocytopenic purpura (TTP), atypical hemolytic uremic syndrome (aHUS), heparin-induced thrombocytopenia, HELLP-syndrome. One of the most important triggers of emergence of a thrombotic microangiopathy is pregnancy. The article describes the clinical observation of atypical hemolytic uremic syndrome in obstetric practice.

关于作者

M. Mochalova
Chita State Medical Academy
俄罗斯联邦


T. Belokrinitskaya
Chita State Medical Academy
俄罗斯联邦


T. Haven
Chita State Clinical Hospital “Regional Clinical Hospital”
俄罗斯联邦


E. Shifman
Vladimirsky MONIKI; Association of Obstetric Anesthesiologists-Reanimatologists
俄罗斯联邦


K. Shapovalov
Chita State Medical Academy
俄罗斯联邦


S. Kostromitin
Chita State Clinical Hospital “Regional Clinical Hospital”
俄罗斯联邦


参考

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ISSN 2218-7332 (Print)
ISSN 2658-3348 (Online)