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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">Bone and soft tissue sarcomas, tumors of the skin</journal-id><journal-title-group><journal-title xml:lang="en">Bone and soft tissue sarcomas, tumors of the skin</journal-title><trans-title-group xml:lang="ru"><trans-title>Саркомы костей, мягких тканей и опухоли кожи</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2219-4614</issn><issn publication-format="electronic">2782-3687</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">479</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>EDITORIAL</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОТ РЕДАКЦИИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Epidemiology of sacral tumors. review</article-title><trans-title-group xml:lang="ru"><trans-title>Эпидемиология опухолей крестца: обзор литературы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Aliev</surname><given-names>M. D.</given-names></name><name xml:lang="ru"><surname>Алиев</surname><given-names>М. Д.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>г. Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Musaev</surname><given-names>E. R.</given-names></name><name xml:lang="ru"><surname>Мусаев</surname><given-names>Э. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>г. Москва</p></bio><email>mer71@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">FGBU N.N. Blokhin Russian Cancer Research Center</institution></aff><aff><institution xml:lang="ru">ФГБУ «Российский онкологический научный центр им. Н.Н. Блохина» РАМН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2014-01-27" publication-format="electronic"><day>27</day><month>01</month><year>2014</year></pub-date><volume>6</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>7</fpage><lpage>15</lpage><history><date date-type="received" iso-8601-date="2022-01-26"><day>26</day><month>01</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-01-26"><day>26</day><month>01</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2014, Aliev M.D., Musaev E.R.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2014, Алиев М.Д., Мусаев Э.Р.</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="en">Aliev M.D., Musaev E.R.</copyright-holder><copyright-holder xml:lang="ru">Алиев М.Д., Мусаев Э.Р.</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://sarbon.abvpress.ru/jour/article/view/479">https://sarbon.abvpress.ru/jour/article/view/479</self-uri><abstract xml:lang="en"><p>Sacral tumors are very rare and consists about 1–7% of all spine tumors. Most of sacral tumors are metastatic tumors, the most often primary malignant tumor of the sacrum is chordoma. Treatment of patient with sacral tumors is still a difficult problem. Most of patients receive treatment from nononcological diseases and referred in specialized hospitals with hugе tumor. The sacrum has a complex anatomy due to its close relationship with major vessels, sacroiliac joints, sacral nerve roots and viscera like the bowel and rectum. This makes it hard to achieve wide surgical margins during surgery and increases perioperative morbidity and mortality. The understanding of tumor behavior will help to develop optimal treatment.</p></abstract><trans-abstract xml:lang="ru"><p>Опухоли крестца встречаются редко и составляют около 17% всех опухолей позвоночного столба. Большинство опухолей крестца метастатической природы, наиболее часто встречающаяся первичная злокачественная опухоль крестца- это хордома. Лечение пациентов с опухолями крестца остается сложной проблемой, большинство пациентов получает лечение в клиниках от неонкологических заболеваний и попадают в специализированные клиники, как правило, уже с опухолями больших размеров . Крестец находится в сложной анатомической зоне, в непосредственной близости к магистральным сосудам, крестцово-подвздошным сочленениям и толстой кишке, что делает сложным достижение широких краев резекции и увеличивает периоперационную смертность. Более детальное изучение этой группы опухолей поможет в разработке правильных алгоритмов лечения.</p></trans-abstract><kwd-group xml:lang="en"><kwd>socral tumors</kwd><kwd>chardoma</kwd><kwd>resection margins</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>опухоли крестца</kwd><kwd>хордома</kwd><kwd>края резекции</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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