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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">nid</journal-id><journal-title-group><journal-title xml:lang="ru">Нефрология и диализ</journal-title><trans-title-group xml:lang="en"><trans-title>Nephrology and Dialysis</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1680-4422</issn><issn pub-type="epub">2618-9801</issn><publisher><publisher-name>Российское диализное общество</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">nid-1039</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>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group></article-categories><title-group><article-title>Обратимость тяжелой почечной недостаточности при миеломной болезни</article-title><trans-title-group xml:lang="en"><trans-title>Recovery of severe renal failure in multiple myeloma</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рехтина</surname><given-names>И. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Rekhtina</surname><given-names>I. G.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Голицина</surname><given-names>Е. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Varshavsky</surname><given-names>E.P. Golitsina.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Варшавский</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Gorchakova</surname><given-names>S. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Горчакова</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Biryukova</surname><given-names>L. S.</given-names></name></name-alternatives><email xlink:type="simple">sgorchakova@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бирюкова</surname><given-names>Л. С.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Гематологический научный центр РАМН</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-2"><institution>ГОУ ВПО Московская медицинская академия им. И.М. Сеченова; г. Москва</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2009</year></pub-date><pub-date pub-type="epub"><day>19</day><month>06</month><year>2025</year></pub-date><volume>11</volume><issue>3</issue><fpage>257</fpage><lpage>262</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Рехтина И.Г., Голицина Е.П., Варшавский В.А., Горчакова С.В., Бирюкова Л.С., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Рехтина И.Г., Голицина Е.П., Варшавский В.А., Горчакова С.В., Бирюкова Л.С.</copyright-holder><copyright-holder xml:lang="en">Rekhtina I.G., Varshavsky E.G., Gorchakova S.V., Biryukova L.S., Бирюкова Л.С.</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://journal.nephro.ru/jour/article/view/1039">https://journal.nephro.ru/jour/article/view/1039</self-uri><abstract><p>В 10% случаев множественная миелома (ММ) дебютирует с тяжелой уремии, требующей заместительной почечной терапии. Обследовано 14 больных с впервые выявленной ММ, у которых заболевание дебютировало с тяжелой стадии почечной недостаточности (ПН). До начала химиотерапии (ХТ) выполнена пункционная биопсия почки с последующей световой, иммунофлуоресцентной и электронной микроскопией. В результате проведенного лечения функция почек улучшилась у 4 (28%) больных, что позволило отказаться от проведения гемодиализа (ГД). У остальных больных улучшения функции почек после ХТ не произошло, продолжается лечение программным ГД. При исследовании биоптатов почки у больных ММ с тяжелой ПН в 50% случаев выявлен сочетанный характер поражения почек в виде цилиндровой нефропатии и отложения моноклональных легких цепей, а также фибриллярной нефропатии. Миеломная нефропатия (МН), как изолированный вариант поражения, диагностирована в 43% случаев. Морфологическим критерием обратимости ПН является отсутствие распространенного интерстициального фиброза. Выраженный интерстициальный фиброз при МН и тяжелой ПН развивается в течение двух-трех месяцев.</p></abstract><trans-abstract xml:lang="en"><p>In 10% of cases Multiple myeloma (MM) begins with severe uremia, thus these patients require renal replacement therapy. We studied 14 patients with newly diagnosed MM. In all these patients the disease debuted with severe stage renal failure. Renal biopsy was performed before chemotherapy with the subsequent light, immunofluorescent and electron microscopy. As a result of the treatment renal function has improved in 4 (28%) patients that allowed us to stop haemodialysis. In other patients after chemotherapy the improvement of renal function has not occurred and haemodialysis has been continued. Study of kidneys biopsies of the patients with MM and severe renal failure in 50% of cases has revealed combined character of renal injury: cast nephropathy and monoclonal light chains deposits, and fibrillar nephropathy. Isolated myeloma nephropathy was diagnosed in 43% of cases. The absence of interstitial fibrosis is the morphological criterion of reversibility of renal failure. Significant interstitial fibrosis in МM patients and severe renal failure develop within two-three months.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>множественная миелома</kwd><kwd>миеломная нефропатия</kwd><kwd>почечная недостаточность</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Бирюкова Л.С., Володяева Е.В., Фетисова Е.В. и др. Острая и хроническая почечная недостаточность у больных миеломной болезнью // Терапевт. арх. 1999. Т. 71. С. № 7. С. 58–64.</mixed-citation><mixed-citation xml:lang="en">Бирюкова Л.С., Володяева Е.В., Фетисова Е.В. и др. Острая и хроническая почечная недостаточность у больных миеломной болезнью // Терапевт. арх. 1999. Т. 71. С. № 7. 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