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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">mrj</journal-id><journal-title-group><journal-title xml:lang="ru">Современная ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Modern Rheumatology Journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1996-7012</issn><issn pub-type="epub">2310-158X</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14412/1996-7012-2024-5-7-15</article-id><article-id custom-type="elpub" pub-id-type="custom">mrj-1634</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ЛЕКЦИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>LECTURE</subject></subj-group></article-categories><title-group><article-title>Фосфопеническая остеомаляция опухолевого генеза: современные подходы к диагностике и лечению</article-title><trans-title-group xml:lang="en"><trans-title>Tumor-induced phosphopenic osteomalacia: modern approaches to diagnostics and treatment</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9152-3234</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кондрашов</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kondrashov</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Артем Александрович Кондрашов</p><p>117513, Москва, ул. Островитянова 1</p></bio><bio xml:lang="en"><p>Artem Aleksandrovich Kondrashov</p><p>1, Ostrovitianov Street, Moscow 117997</p></bio><email xlink:type="simple">kaartem@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8266-6022</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Андрияшкина</surname><given-names>Д. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Andriyashkina</surname><given-names>D. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>117513, Москва, ул. Островитянова 1</p></bio><bio xml:lang="en"><p>1, Ostrovitianov Street, Moscow 117997</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6890-8777</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Демидова</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Demidova</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>117513, Москва, ул. Островитянова 1</p></bio><bio xml:lang="en"><p>1, Ostrovitianov Street, Moscow 117997</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0457-8921</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Саакян</surname><given-names>Ю. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Sahakyan</surname><given-names>Yu. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>117513, Москва, ул. Островитянова 1</p></bio><bio xml:lang="en"><p>1, Ostrovitianov Street, Moscow 117997</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7410-9784</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Клименко</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Klimenko</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>117513, Москва, ул. Островитянова 1</p></bio><bio xml:lang="en"><p>1, Ostrovitianov Street, Moscow 117997</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГАОУ ВО «Российский национальный  исследовательский медицинский университет им. Н.И. Пирогова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Pirogov Russian National Research Medical University, Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГАОУ ВО «Российский национальный исследовательский медицинский университет им. Н.И. Пирогова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Pirogov Russian National Research Medical University, Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>19</day><month>10</month><year>2024</year></pub-date><volume>18</volume><issue>5</issue><fpage>7</fpage><lpage>15</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Кондрашов А.А., Андрияшкина Д.Ю., Демидова Н.А., Саакян Ю.М., Клименко А.А., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Кондрашов А.А., Андрияшкина Д.Ю., Демидова Н.А., Саакян Ю.М., Клименко А.А.</copyright-holder><copyright-holder xml:lang="en">Kondrashov A.A., Andriyashkina D.Y., Demidova N.A., Sahakyan Y.M., Klimenko A.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://mrj.ima-press.net/mrj/article/view/1634">https://mrj.ima-press.net/mrj/article/view/1634</self-uri><abstract><p>Фосфопеническая остеомаляция (ФПОМ) – редкий вариант паранеопластического синдрома, возникающий при синтезе опухолью фактора роста фибробластов (ФРФ) 23. Под действием ФРФ23 происходит снижение реабсорбции фосфатов, уровня кальцитриола, что приводит к развитию выраженной гипофосфатемии и гипокальциемии. Синтез ФРФ23 ассоциирован преимущественно с доброкачественными мезенхимальными опухолями, однако описан и для злокачественных новообразований. Основными клиническими проявлениями ФПОМ являются генерализованная миалгия и миопатия, оссалгия, патологические переломы и др. Диагностика заболевания предполагает поэтапное обследование с применением методов визуализации, основанных на идентификации рецепторов соматостатина, поскольку именно они обладают самой высокой чувствительностью для выявления новообразований, вызывающих остеомаляцию. Хирургическое вмешательство, безусловно, является предпочтительным методом лечения. К перспективным нехирургическим методам можно отнести лечение буросумабом и аналогами соматостатина.</p></abstract><trans-abstract xml:lang="en"><p>Phosphopenic osteomalacia (PPOM) is a rare variant of paraneoplastic syndrome caused by tumor synthesis of fibroblast growth factor 23 (FGF23). FGF23 secretion leads to a decrease in phosphate reabsorption and calcitriol levels, which leads to the development of severe hypophosphataemia and hypocalcaemia. FGF23 synthesis is predominantly associated with benign mesenchymal tumors, but has also been described in malignant neoplasms. The main clinical manifestations of PPOM are generalized myalgias and myopathy, ostealgia, pathological fractures, etc. The diagnosis of the disease requires a step-by-step investigation using somatostatin receptor-based imaging techniques, as these have the highest sensitivity for the detection of neoplasms causing osteomalacia. Surgical intervention is clearly the treatment of choice. Promising non-surgical methods include treatment with burosumab and somatostatin analogues.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>остеомаляция</kwd><kwd>гипофосфатемия</kwd><kwd>фосфопеническая остеомаляция</kwd><kwd>опухоль-индуцированная остеомаляция</kwd><kwd>фактор роста фибробластов 23 (ФРФ23)</kwd><kwd>переломы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>osteomalacia</kwd><kwd>hypophosphatemia</kwd><kwd>phosphopenic osteomalacia</kwd><kwd>tumour-induced osteomalacia</kwd><kwd>fibroblast growth factor 23 (FGF23)</kwd><kwd>fractures</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование не имело спонсорской поддержки.</funding-statement><funding-statement xml:lang="en">The investigation has not been sponsored.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Bhatt AA, Mathews SS, Kumari A, Paul TV. 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