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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">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">265</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2019-18-3-88-95</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>CLINICAL OBSERVATIONS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Invasive aspergillosis in children in debut of acute myeloid leukemia</article-title><trans-title-group xml:lang="ru"><trans-title>Инвазивный аспергиллез у детей в дебюте острого миелобластного лейкоза</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2003-0982</contrib-id><name-alternatives><name xml:lang="en"><surname>Dinikina</surname><given-names>Y. V.</given-names></name><name xml:lang="ru"><surname>Диникина</surname><given-names>Ю. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><bold>Yulia V. Dinikina,</bold> MD, PhD, Head of the Department of pediiatric oncohematology and SCT Almazov National Medical Research Centre, St. Petersburg</p><p><italic>197341, St. Petersburg, </italic><italic>А</italic><italic>kkuratova st., 2 </italic><italic/></p></bio><bio xml:lang="ru"><p><bold>Диникина Юлия Валерьевна</bold>, кандидат медицинских наук, заведующая отделением химиотерапии онкогематологических заболеваний и ТКМ для детей НМИЦ им. В.А. Алмазова Минздрава России</p><p><italic>197341, Санкт-Петербург, ул. Аккуратова, 2 </italic><italic/></p></bio><email>dinikina_yuv@almazovcentre.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shadrivova</surname><given-names>O. V.</given-names></name><name xml:lang="ru"><surname>Шадривова</surname><given-names>О. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Saint-Petersburg</italic></p></bio><bio xml:lang="ru"><p><italic>Санкт-Петербург</italic></p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7471-7181</contrib-id><name-alternatives><name xml:lang="en"><surname>Belogurova</surname><given-names>M. B.</given-names></name><name xml:lang="ru"><surname>Белогурова</surname><given-names>М. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Saint-Petersburg</italic></p></bio><bio xml:lang="ru"><p><italic>Санкт-Петербург</italic></p></bio><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Dokhina</surname><given-names>N. N.</given-names></name><name xml:lang="ru"><surname>Дохина</surname><given-names>Н. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Saint-Petersburg</italic></p></bio><bio xml:lang="ru"><p><italic>Санкт-Петербург</italic></p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Khostelidi</surname><given-names>S. N.</given-names></name><name xml:lang="ru"><surname>Хостелиди</surname><given-names>С. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Saint-Petersburg</italic></p></bio><bio xml:lang="ru"><p><italic>Санкт-Петербург</italic></p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0306-3694</contrib-id><name-alternatives><name xml:lang="en"><surname>Ignatyeva</surname><given-names>S. M.</given-names></name><name xml:lang="ru"><surname>Игнатьева</surname><given-names>С. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Saint-Petersburg</italic></p></bio><bio xml:lang="ru"><p><italic>Санкт-Петербург</italic></p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2450-687X</contrib-id><name-alternatives><name xml:lang="en"><surname>Bogomolova</surname><given-names>T. S.</given-names></name><name xml:lang="ru"><surname>Богомолова</surname><given-names>Т. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Saint-Petersburg</italic></p></bio><bio xml:lang="ru"><p><italic>Санкт-Петербург</italic></p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6095-7531</contrib-id><name-alternatives><name xml:lang="en"><surname>Klimko</surname><given-names>N. N.</given-names></name><name xml:lang="ru"><surname>Климко</surname><given-names>Н. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Saint-Petersburg</italic></p></bio><bio xml:lang="ru"><p><italic>Санкт-Петербург</italic></p></bio><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Almazov National Medical Research Centre of the Ministry of Healthcare of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр им. В.А. Алмазова» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">St. Petersburg State Pediatric Medical University, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВПО «Санкт-Петербургский государственный педиатрический медицинский университет», Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">North-Western State Medical University named after I.I. Mechnikov</institution></aff><aff><institution xml:lang="ru">ФГБУ ВО «Северо-Западный государственный медицинский университет им. И.И. Мечникова»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-09-13" publication-format="electronic"><day>13</day><month>09</month><year>2019</year></pub-date><volume>18</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>88</fpage><lpage>95</lpage><history><date date-type="received" iso-8601-date="2019-09-13"><day>13</day><month>09</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-09-13"><day>13</day><month>09</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2019, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2019, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/265">https://hemoncim.com/jour/article/view/265</self-uri><abstract xml:lang="en"><p>Invasive aspergillosis (IA) is a life-threatening complication in pediatric patients with hematological malignancies. The highest incidence rates of IA were found in pediatric patients with acute myeloid leukemia (AML). We presented a case of successful treatment of IA in a patient with debut of AML with Down syndrome, analysis of IA cases in children with AML according data of the register and a literature review. 46 pediatric patients with IA were included, among them 16 (34.7%) with AML. In 3 (18.75%) pts AML was diagnosed in presentation of AML. Risk factors of IA were prolonged neutropenia (100%) and lymphocytopenia (81%). The most common clinical signs were: fever &gt; 38.5 ºС (93.7%), cough (75%) and respiratory failure (43.7%). The lung involvement was diagnosed in 93.7% of pts, more than 2 sites of IA – in 12.5%, endophthalmitis – in 6.25%. Typical imaging finding was «halo sign» – 37.5%. According received results «probable IA» was diagnosed in 87.5% of pts and «proven» in 12.5%. Antifungal treatment received 100% of patients, with voriconazole only – 50%, combined antifungal therapy – 33.3%. Overall 12-week survival was 87.5%. Parents patients agreed to use personal data in research and publications.</p></abstract><trans-abstract xml:lang="ru"><p>Инвазивный аспергиллез (ИА) – угрожающее жизни осложнение у детей с онкогематологическими заболеваниями. Риск развития ИА наиболее высок у больных с острым миелоидным лейкозом (ОМЛ). В статье представлен случай успешного лечения ИА в дебюте ОМЛ у пациента с синдромом Дауна, а также анализ ИА у детей с ОМЛ по данным регистра и обзор литературы. Общее число пациентов – 46, из них с ОМЛ – 16 (34,7%); ИА диагностировали в дебюте ОМЛ у 3 (18,75%) пациентов. Факторами риска развития ИА были длительный агранулоцитоз (100%) и лимфоцитопения (81%). Основные клинические проявления: повышение температуры тела выше 38,5 ºС (93,7%), кашель (75%) и дыхательная недостаточность (43,7%). Поражение легких отмечено у 93,7% больных; более двух очагов поражения – у 12,5%; эндофтальмит – у 6,25%. На основании результатов обследования «вероятный» ИА был диагностирован у 87,5%, «доказанный» – у 12,5% больных. Антимикотическую терапию получили 100% пациентов, монотерапию вориконазолом – 50%, комбинацию антимикотиков – 33,3%. Общая 12-недельная выживаемость составила 87,5%. Родители дали согласие на использование информации в научных исследованиях и публикациях.</p></trans-abstract><kwd-group xml:lang="en"><kwd>invasive aspergillosis</kwd><kwd>children</kwd><kwd>oncohematology</kwd><kwd>acute leukemia</kwd><kwd>antifungal therapy</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>инвазивный аспергиллез</kwd><kwd>дети</kwd><kwd>онкогематология</kwd><kwd>острый лейкоз</kwd><kwd>антифунгальная терапия</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.	Miller D.R., Miller L.P. Acute lymphoblastic leukemia in children: an update of clinical, biological, and therapeutic aspects. Crit Rev Oncol Hematol 1990; 10 (2): 131–64.</mixed-citation><mixed-citation xml:lang="ru">Miller D.R., Miller L.P. Acute lymphoblastic leukemia in children: an update of clinical, biological, and therapeutic aspects. 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