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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medbio</journal-id><journal-title-group><journal-title xml:lang="ru">Медико-биологические проблемы жизнедеятельности</journal-title><trans-title-group xml:lang="en"><trans-title>Medical and Biological Problems of Life Activity</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2074-2088</issn><publisher><publisher-name>Республиканский научно-практический центр радиационной медицины и экологии человека</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">medbio-222</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБМЕН ОПЫТОМ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>EXPERIENCE EXCHANGE</subject></subj-group></article-categories><title-group><article-title>Клинический случай приобретенной формы тромботической тромбоцитопенической пурпуры: диагностический поиск и лечение</article-title><trans-title-group xml:lang="en"><trans-title>A clinical case of acquired form of thrombotic thrombocytopenic purpura. Description and treatment</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Новик</surname><given-names>Д. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Novik</surname><given-names>D. K.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Денисов</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Denisov</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Репченко</surname><given-names>Е. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Repchenko</surname><given-names>E. M.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кравченко</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kravchenko</surname><given-names>D. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кузнецов</surname><given-names>С. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuzniatsou</surname><given-names>S. G.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хаданович</surname><given-names>С. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Khadanovich</surname><given-names>S. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>ГУ «РНПЦ радиационной медицины и экологии человека»</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>02</day><month>03</month><year>2023</year></pub-date><volume>0</volume><issue>2</issue><fpage>124</fpage><lpage>128</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Новик Д.К., Денисов А.В., Репченко Е.М., Кравченко Д.В., Кузнецов С.Г., Хаданович С.А., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Новик Д.К., Денисов А.В., Репченко Е.М., Кравченко Д.В., Кузнецов С.Г., Хаданович С.А.</copyright-holder><copyright-holder xml:lang="en">Novik D.K., Denisov A.V., Repchenko E.M., Kravchenko D.V., Kuzniatsou S.G., Khadanovich S.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://medbio.ejournal.by/jour/article/view/222">https://medbio.ejournal.by/jour/article/view/222</self-uri><abstract><p>В настоящей статье изложен клинический случай приобретенной формы тромботической тромбоцитопенической пурпуры. Описаны симптоматика данного редкого заболевания и проводимое лечение. Диагноз был выставлен по минимальным диагностическим критериям и в процессе лечения был получен хороший терапевтический ответ.</p></abstract><trans-abstract xml:lang="en"><p>In the article have described symptoms and ongoing treatment of the acquired form of thrombotic thrombocytopenic purpura.Thrombotic thrombocytopenic purpura is a rare disease with a frequency of 4:1000000 population. It is characterized by an extremely aggressive course and high mortality in the absence of treatment (up to 90%). Often has no specific symptoms. The condition for clinical diagnosis (in the absence of other causes) is the presence of at least two symptoms: thrombocytopenia, microangiopathic hemolytic anemia.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>тромботическая тромбоцитопеническая пурпура</kwd><kwd>тромбоцитопения</kwd><kwd>фактор Виллебранда</kwd><kwd>плазмаферез</kwd></kwd-group><kwd-group xml:lang="en"><kwd>thrombotic thrombocytopenic purpura</kwd><kwd>thrombocytopenia</kwd><kwd>Willebrand factor</kwd><kwd>plasmapheresis</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Филатов, Л.Б. Тромботическая тромбоцитопеническая пурпура (болезнь Мошковица) / Л.Б. Филатов // Редкие гематологические болезни и синдромы. Под ред. М.А. Волковой. - М.: Практическая медицина, 2011. - С. 32-51.</mixed-citation><mixed-citation xml:lang="en">Филатов, Л.Б. 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