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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">Head and Neck Tumors</journal-id><journal-title-group><journal-title xml:lang="en">Head and Neck Tumors</journal-title><trans-title-group xml:lang="ru"><trans-title>Опухоли головы и шеи</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2222-1468</issn><issn publication-format="electronic">2411-4634</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">73</article-id><article-id pub-id-type="doi">10.17650/2222-1468-2012-0-2-92-96</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРНАЯ СТАТЬЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">CURRENT APPROACHES TO TREATING NON-RHABDOID SOFT TISSUE SARCOMAS OF THE HEAD AND NECK IN CHILDREN: A REVIEW OF LITERATURE</article-title><trans-title-group xml:lang="ru"><trans-title>СОВРЕМЕННЫЕ ПОДХОДЫ К ЛЕЧЕНИЮ НЕРАБДОИДНЫХ САРКОМ МЯГКИХ ТКАНЕЙ ГОЛОВЫ И ШЕИ У ДЕТЕЙ (ОБЗОР ЛИТЕРАТУРЫ)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bolotin</surname><given-names>M. V.</given-names></name><name xml:lang="ru"><surname>Болотин</surname><given-names>М. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>bolotin1980@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Lopatin</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Лопатин</surname><given-names>А. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Russian Children’s Clinical Hospital, Ministry of Health of Russia, Moscow</institution></aff><aff><institution xml:lang="ru">ФГБУ «Российская детская клиническая больница» Минздрава России, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2012-04-15" publication-format="electronic"><day>15</day><month>04</month><year>2012</year></pub-date><volume>2</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>92</fpage><lpage>96</lpage><history><date date-type="received" iso-8601-date="2015-04-18"><day>18</day><month>04</month><year>2015</year></date><date date-type="accepted" iso-8601-date="2015-04-18"><day>18</day><month>04</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2012, Bolotin M.V., Lopatin A.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2012, Болотин М.В., Лопатин А.В.</copyright-statement><copyright-year>2012</copyright-year><copyright-holder xml:lang="en">Bolotin M.V., Lopatin A.V.</copyright-holder><copyright-holder xml:lang="ru">Болотин М.В., Лопатин А.В.</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://ogsh.abvpress.ru/jour/article/view/73">https://ogsh.abvpress.ru/jour/article/view/73</self-uri><abstract xml:lang="en"><p>Soft tissue sarcomas constitute approximately 8–10 % of all malignancies in children and adolescents and half of them are rhabdomyosarcoma. The second half makes up a heterogeneous group of malignancies of mesenchymal non-rhabdoid origin, which have been recently referred to as an individual group of non-rhabdoid soft tissue sarcomas (an adult type) in increasing frequency. The choice of a treatment option depends on a number of factors: its histological structure, location, stage of a tumor; the possible performance of radical surgery; and the grade of tumor differentiation. Surgery is the basic treatment; if it is impossible, chemoradiotherapy is performed at stage 1. </p></abstract><trans-abstract xml:lang="ru"><p>Саркомы мягких тканей составляют около 8–10 % всех злокачественных опухолей у детей и подростков и половина из них представлена рабдомиосаркомой. Вторая половина представлена гетерогенной группой злокачественных опухолей мезенхимального нерабдоидного происхождения, которые в последнее время все чаще выделяются в отдельную группу нерабдоидных сарком мягких тканей («взрослый тип»). Выбор метода лечения зависит от ряда факторов — гистологического строения, локализации образования; стадии; возможности выполнения радикального оперативного вмешательства; степени дифференцировки опухоли. Основной метод лечения — оперативное вмешательство, при его невозможности на первом этапе проводится химиолучевое лечение.</p></trans-abstract><kwd-group xml:lang="en"><kwd>non-rhabdoid soft tissue sarcomas</kwd><kwd>children</kwd><kwd>head and neck tumors</kwd><kwd>principles of treatment and diagnosis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>нерабдоидные саркомы мягких тканей</kwd><kwd>дети</kwd><kwd>опухоли головы и шеи</kwd><kwd>принципы лечения и диагностики</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. Ferrari A., Casanova M. Specification on the definition of adult-type soft tissue sarcoma. 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