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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">536</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2022-17-2-36-42</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>RARE AND COMPLEX CLINICAL SITUATIONS: DIAGNOSTIC DIFFICULTIE AND TREATMENT CHOICE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>РЕДКИЕ И СЛОЖНЫЕ КЛИНИЧЕСКИЕ СИТУАЦИИ: ТРУДНОСТИ ДИАГНОСТИКИ И ВЫБОР ТАКТИКИ ЛЕЧЕНИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">A rare case of an anaphylactic reaction to plasma and recombinant blood coagulation factor VIII in a child with severe hemophilia A</article-title><trans-title-group xml:lang="ru"><trans-title>Редкий случай анафилактической реакции на введение плазменного и рекомбинантного фактора свертывания крови VIII у ребенка с тяжелой формой гемофилии А</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2738-429X</contrib-id><name-alternatives><name xml:lang="en"><surname>Dmitriev</surname><given-names>V. V.</given-names></name><name xml:lang="ru"><surname>Дмитриев</surname><given-names>В. В.</given-names></name></name-alternatives><address><country country="BY">Belarus</country></address><bio xml:lang="en"><p><italic>223053, Minsk region, Borovlyany, Frunzenskaya St., 43</italic></p></bio><bio xml:lang="ru"><p><italic>223053 Минский район, д. Боровляны, ул. Фрунзенская, 43</italic></p></bio><email>dmitrievhaematol@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Naumovich</surname><given-names>M. G.</given-names></name><name xml:lang="ru"><surname>Наумович</surname><given-names>М. Г.</given-names></name></name-alternatives><address><country country="BY">Belarus</country></address><bio xml:lang="en"><p><italic>223053, Minsk region, Borovlyany, Frunzenskaya St., 43</italic></p></bio><bio xml:lang="ru"><p><italic>223053 Минский район, д. Боровляны, ул. Фрунзенская, 43</italic></p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0233-7718</contrib-id><name-alternatives><name xml:lang="en"><surname>Dmitriev</surname><given-names>E. V.</given-names></name><name xml:lang="ru"><surname>Дмитриев</surname><given-names>Е. В.</given-names></name></name-alternatives><address><country country="BY">Belarus</country></address><bio xml:lang="en"><p><italic>223053, Minsk region, Borovlyany, Frunzenskaya St., 43</italic></p></bio><bio xml:lang="ru"><p><italic>223053 Минский район, д. Боровляны, ул. Фрунзенская, 43</italic></p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Belarusian Research Center for Pediatric Oncology, Hematology and Immunology</institution></aff><aff><institution xml:lang="ru">ГУ «Республиканский научно-практический центр детской онкологии, гематологии и иммунологии» Минздрава Республики Беларусь</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-04-14" publication-format="electronic"><day>14</day><month>04</month><year>2022</year></pub-date><volume>17</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>36</fpage><lpage>42</lpage><history><date date-type="received" iso-8601-date="2022-04-12"><day>12</day><month>04</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-04-12"><day>12</day><month>04</month><year>2022</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/536">https://oncohematology.abvpress.ru/ongm/article/view/536</self-uri><abstract xml:lang="en"><p>A rare case of anaphylactic shock after administration of 4<sup>th</sup> generation recombinant blood coagulation factor VIII is presented. Anaphylactic shock is a life-threatening complication for a patient with hemophilia A. Temporarily refrain from re-administration of factor VIII, a skin test confirming drug choice, and a patient desensitization procedure provide the clinician with a chance to continue hemostatic replacement therapy for a patient with hemophilia A.The main purpose of this case report is to determine the algorithm of actions to overcome the consequences of anaphylactic shock and continue the prophylactic administration of coagulation factor VIII concentrate to prevent bleeding in a child with a rare random combination of an anaphylactic reaction and congenital coagulation disorders.</p></abstract><trans-abstract xml:lang="ru"><p>Представлен редкий случай анафилактического шока на введение лекарственного средства, содержащего рекомбинантный фактор свертывания крови VIII 4-го поколения. Анафилактический шок представляет серьезную опасность для жизни пациента с гемофилией А. Временное воздержание от повторного введения фактора свертывания VIII, кожная проба, подтверждающая возможность выбора лекарственного средства, и процедура десенсибилизации пациента предоставляют врачу шанс продолжения заместительной гемостатической терапии у пациента с гемофилией А.Основная цель наблюдения заключается в определении порядка действий по преодолению последствий анафилактического шока и продолжения профилактического введения концентрата фактора свертывания крови VIII для предупреждения кровотечений у ребенка с редким случайным сочетанием анафилактической реакции и врожденных нарушений свертывания крови.</p></trans-abstract><kwd-group xml:lang="en"><kwd>children</kwd><kwd>severe form of hemophilia A</kwd><kwd>hemostatic replacement therapy</kwd><kwd>anaphylactic reaction</kwd><kwd>pathological clotting inhibitor</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>дети</kwd><kwd>тяжелая форма гемофилии А</kwd><kwd>заместительная гемостатическая терапия</kwd><kwd>анафилактическая реакция</kwd><kwd>патологический ингибитор свертывания</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. 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