Clinical case of thrombotic microangiopathy in obstetric practice

Autor:	M. N. Mochalova, T. E. Belokrinitskaya, T. V. Haven, E. M. Shifman, K. G. Shapovalov, S. V. Kostromitin
Jazyk:	ruština
Rok vydání:	2017
Předmět:	preeclampsia Medicine (General) R5-920 atypical hemolytic uremic syndrome hemic and lymphatic diseases thrombotic thrombocytopenic purpura hellp-syndrome hellp-синдром thrombotic microangiopathy
Zdroj:	Сеченовский вестник, Vol 0, Iss 2, Pp 28-32 (2017)
ISSN:	2658-3348 2218-7332
Popis:	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.
Databáze:	OpenAIRE
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