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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">360</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>BONE SARCOMAS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>САРКОМЫ КОСТЕЙ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Low-grade central osteosarcoma. Review</article-title><trans-title-group xml:lang="ru"><trans-title>Центральная остеосаркома с низким злокачественным потенциалом. Обзор литературы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Rogozhin</surname><given-names>D. V.</given-names></name><name xml:lang="ru"><surname>Рогожин</surname><given-names>Д. В.</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>Pathol.777@mail.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>Konovalov</surname><given-names>D. M.</given-names></name><name xml:lang="ru"><surname>Коновалов</surname><given-names>Д. М.</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"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Talalaev</surname><given-names>A. G.</given-names></name><name xml:lang="ru"><surname>Талалаев</surname><given-names>А. Г.</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"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Roschin</surname><given-names>V. Yu.</given-names></name><name xml:lang="ru"><surname>Рощин</surname><given-names>В. Ю.</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"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bolshakov</surname><given-names>N. A.</given-names></name><name xml:lang="ru"><surname>Большаков</surname><given-names>Н. А.</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="aff3"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Tikhonova</surname><given-names>M. V.</given-names></name><name xml:lang="ru"><surname>Тихонова</surname><given-names>М. В.</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="aff5"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Remizov</surname><given-names>A. N.</given-names></name><name xml:lang="ru"><surname>Ремизов</surname><given-names>А. Н.</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="aff5"/><xref ref-type="aff" rid="aff4"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Russian Children’s Clinical Hospital</institution></aff><aff><institution xml:lang="ru">ФГБУ «Российская детская клиническая больница»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Research Center of Pediatric Hematology, Oncology and Immunology</institution></aff><aff><institution xml:lang="ru">ФГБУ «Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Д. Рогачева»</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Russian Children’s Clinical Hospital</institution></aff><aff><institution xml:lang="ru">ФГБУ «Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Д. Рогачева»</institution></aff></aff-alternatives><aff id="aff4"><institution>Research Center of Pediatric Hematology, Oncology and Immunology</institution></aff><aff id="aff5"><institution>Russian Children’s Clinical Hospital</institution></aff><pub-date date-type="pub" iso-8601-date="2016-10-22" publication-format="electronic"><day>22</day><month>10</month><year>2016</year></pub-date><volume>8</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>16</fpage><lpage>21</lpage><history><date date-type="received" iso-8601-date="2022-01-22"><day>22</day><month>01</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-01-22"><day>22</day><month>01</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2016, Rogozhin D.V., Konovalov D.M., Talalaev A.G., Roschin V.Y., Bolshakov N.A., Tikhonova M.V., Remizov A.N.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2016, Рогожин Д.В., Коновалов Д.М., Талалаев А.Г., Рощин В.Ю., Большаков Н.А., Тихонова М.В., Ремизов А.Н.</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="en">Rogozhin D.V., Konovalov D.M., Talalaev A.G., Roschin V.Y., Bolshakov N.A., Tikhonova M.V., Remizov A.N.</copyright-holder><copyright-holder xml:lang="ru">Рогожин Д.В., Коновалов Д.М., Талалаев А.Г., Рощин В.Ю., Большаков Н.А., Тихонова М.В., Ремизов А.Н.</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/360">https://sarbon.abvpress.ru/jour/article/view/360</self-uri><abstract xml:lang="en"><p>Low-grade central osteosarcoma is a rare subtype of intramedullary osteosarcoma (approximately 1% of all osteosarcomas) that characterized histologically by a spindle cell proliferation associated with trabecular bone formation, and is usually located in the long bones with a predilection for the distal femur and proximal tibia. It has the potential to recur, dedifferentiate, and metastasize subsequent to surgical treatment. Sometimes it is difficult to make a diagnosis and differentiate it with fibrous dysplasia and desmoplastic fibroma. In such cases, careful radiological interpretation is helpful. This tumor usually carries a good prognosis.</p></abstract><trans-abstract xml:lang="ru"><p>Центральная остеосаркома с низким потенциалом злокачественности – это интрамедуллярная злокачественная опухоль костей (составляет порядка 1% среди всех остеосарком), состоящая из веретеновидных неопластических клеток с наличием костного компонента (остеоида или костной ткани). Локализуется чаще всего в длинных трубчатых костях с преобладанием в дистальной части бедренной кости и проксимальной части большеберцовой кости. Может локально рецидивировать, подвергаться дедифференцировке или метастазировать после хирургического лечения. В некоторых случаях представляет сложности в дифференциальной диагностике с фиброзной дисплазией и десмопластической фибромой. Имеет хороший прогноз.</p></trans-abstract><kwd-group xml:lang="en"><kwd>low-grade central osteosarcoma</kwd><kwd>fibrous dysplasia</kwd><kwd>desmoplastic fibroma</kwd><kwd>differential diagnostic</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>центральная остеосаркома с низким злокачественным потенциалом</kwd><kwd>фиброзная дисплазия</kwd><kwd>десмопластическая фиброма</kwd><kwd>дифференциальная диагностика</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. Picci P., Manfrini M., Fabbri N., Gambarotti M., Vanel D. Atlas of Musculoskeletal Tumors and Tumorlike Lesions. The Rizzoli Case Archive. 2014, p. 181-184.</mixed-citation><mixed-citation xml:lang="ru">Picci P., Manfrini M., Fabbri N., Gambarotti M., Vanel D. 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