Сеченовский вестник (Jun 2017)

Clinical case of thrombotic microangiopathy in obstetric practice

  • M. N. Mochalova,
  • T. E. Belokrinitskaya,
  • T. V. Haven,
  • E. M. Shifman,
  • K. G. Shapovalov,
  • S. V. Kostromitin

Journal volume & issue
Vol. 0, no. 2
pp. 28 – 32

Abstract

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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.

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