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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">vsp</journal-id><journal-title-group><journal-title xml:lang="ru">Вопросы современной педиатрии</journal-title><trans-title-group xml:lang="en"><trans-title>Current Pediatrics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-5527</issn><issn pub-type="epub">1682-5535</issn><publisher><publisher-name>Издательство «ПедиатрЪ»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15690/vsp.v22i6.2649</article-id><article-id custom-type="elpub" pub-id-type="custom">vsp-3356</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>КЛИНИЧЕСКОЕ НАБЛЮДЕНИЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL OBSERVATIONS</subject></subj-group></article-categories><title-group><article-title>Применение белимумаба у пациентки с системной красной волчанкой с ювенильным дебютом и стероидным диабетом: клинический случай</article-title><trans-title-group xml:lang="en"><trans-title>Belimumab in a Patient with Systemic Lupus Erythematosus with Juvenile Onset and Steroid-induced Diabetes: Clinical Case</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0513-6826</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каледа</surname><given-names>М. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Kaleda</surname><given-names>Maria I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Каледа Мария Игоревна - кандидат медицинских наук, старший научный сотрудник лаборатории ревматических заболеваний детского возраста НИИ ревматологии им. В.А. Насоновой.</p><p>Адрес: 115522, Москва, Каширское шоссе, д. 34А</p><p>Тел.: +7 (495) 109-29-10</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">kaleda-mi@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1842-0348</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Никишина</surname><given-names>И. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikishina</surname><given-names>Irina P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</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/0009-0002-0402-3640</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Фирса</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Firsa</surname><given-names>Alesya V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»<country>Россия</country></aff><aff xml:lang="en">Research Institute of Rheumatology named after V.A. Nasonova<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>12</day><month>01</month><year>2024</year></pub-date><volume>22</volume><issue>6</issue><fpage>546</fpage><lpage>553</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Каледа М.И., Никишина И.П., Фирса А.В., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Каледа М.И., Никишина И.П., Фирса А.В.</copyright-holder><copyright-holder xml:lang="en">Kaleda M.I., Nikishina I.P., Firsa A.V.</copyright-holder><license 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://vsp.spr-journal.ru/jour/article/view/3356">https://vsp.spr-journal.ru/jour/article/view/3356</self-uri><abstract><p>Обоснование. Лечение детей с системной красной волчанкой (СКВ), как правило, сопряжено с пожизненным приемом системных глюкокортикоидов и, как следствие, высоким риском серьезных побочных эффектов, в том числе развития стероидного диабета. Применение белимумаба, ингибитора активности стимулятора В-лимфоцитов, позволяет существенно снизить дозу глюкокортикоидов, риск и тяжесть осложнений стероидной терапии. Описание клинического случая. Диагноз СКВ у пациентки установлен в возрасте 16 лет. Начата терапия гидроксихлорохином и пероральным глюкокортикоидом в высокой дозе (56 мг метилпреднизолона в сутки). Через 1 мес от начала терапии диагностирован стероидный диабет, через 2 мес обнаружены участки аваскулярного некроза. На фоне терапии микофенолата мофетилом удалось добиться купирования активности заболевания. Однако в связи с сохранением потребности в инсулине и прогрессированием аваскулярного некроза через 5 мес после верификации диагноза назначен белимумаб. Заключение. Белимумаб — единственный генно-инженерный биологический препарат, зарегистрированный для лечения детей с СКВ. В результате его назначения удалось быстро (в течение 3 мес) стабилизировать состояние пациентки, существенно снизить дозу перорального глюкокортикоида метилпреднизолона (с 24 до 8 мг/сут), добиться ремиссии стероидного диабета с отменой инсулина, а также купировать клинические симптомы аваскулярного некроза.</p></abstract><trans-abstract xml:lang="en"><p>Background. The management of children with systemic lupus erythematosus (SLE) is usually associated with lifelong systemic glucocorticoids administration and, thereby, high risk of serious side effects, including steroid-induced diabetes. The belimumab (B-lymphocyte stimulator inhibitor) administration significantly reduces the glucocorticoids dose, the risk and severity of steroid therapy complications. Clinical case description. The patient was diagnosed with SLE at the age of 16 years. Therapy with hydroxychloroquine and oral glucocorticoid at a high dose (methylprednisolone 56 mg per day) was initiated. Steroid-induced diabetes was diagnosed 1 month after the therapy start; avascular necrosis sites were revealed in 2 months. Mycophenolate mofetil made it possible to achieve the disease activity control. However, the belimumab was prescribed 5 months after diagnosis verification due to continuous insulin requirement and avascular necrosis progression. Conclusion. Belimumab is the only genetically engineered biologic drug approved for the treatment of children with SLE. As a result of its use, it was possible to stabilize the patient's condition quickly (within 3 months), to reduce significantly the dose of oral glucocorticoid, methylprednisolone (from 24 to 8 mg/day), to achieve remission of steroidinduced diabetes with further insulin withdrawal, and also to relieve avascular necrosis clinical symptoms.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>системная красная волчанка с ювенильным началом</kwd><kwd>пероральные глюкокортикоиды</kwd><kwd>стероидный диабет</kwd><kwd>аваскулярный некроз</kwd><kwd>белимумаб</kwd></kwd-group><kwd-group xml:lang="en"><kwd>systemic lupus erythematosus with juvenile onset</kwd><kwd>oral glucocorticoids</kwd><kwd>steroid-induced diabetes</kwd><kwd>avascular necrosis</kwd><kwd>belimumab</kwd></kwd-group><funding-group xml:lang="ru"><funding-statement>Подготовка рукописи выполнена в рамках фундаментальной научной темы (исследования, выполняемого в рамках государственного задания) № 1021051302580-4 в НИИ ревматологии им. В.А. Насоновой. Авторы выражают благодарность за помощь в обследовании и лечении пациентки сотрудникам Национального медицинского исследовательского центра эндокринологии — заместителю главного врача к.м.н. Г.Н. Светловой, заведующему детским отделением сахарного диабета д.м.н. Д.Н. Лаптеву, сотрудникам отделения лучевой диагностики НИИ ревматологии им. В.А. Насоновой.</funding-statement></funding-group><funding-group xml:lang="en"><funding-statement>The manuscript was prepared within the fundamental research topic (research within the state assignment) No. 1021051302580-4 at the Research Institute of Rheumatology named after V.A. Nasonova. The authors express gratitude to the employees of the National Medical Research Center of Endocrinology — deputy head physician, candidate of medicine, G.N. Svetlova, head of pediatric department of diabetes mellitus, doctor of medicine, D.N. Laptev, and diagnostic radiology department of Research Institute of Rheumatology named after V.A. 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