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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">problendo</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы Эндокринологии</journal-title><trans-title-group xml:lang="en"><trans-title>Problems of Endocrinology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0375-9660</issn><issn pub-type="epub">2308-1430</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/probl11816</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-11816</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>Низкорослость и лечение ее гормоном роста</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Dwarfism and its Therapy with Growth Hormone</subject></subj-group></article-categories><title-group><article-title>Частота рецидивов краниофарингиомы у детей, получавших лечение гормоном роста</article-title><trans-title-group xml:lang="en"><trans-title>Incidence of craniopharyngioma relapses in children treated with growth hormone</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>Вилтон</surname><given-names>П</given-names></name><name name-style="western" xml:lang="en"><surname>Wilton</surname><given-names>P</given-names></name></name-alternatives><email xlink:type="simple">probl@endojournals.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Прайс</surname><given-names>Д А</given-names></name><name name-style="western" xml:lang="en"><surname>Price</surname><given-names>D A</given-names></name></name-alternatives><email xlink:type="simple">probl@endojournals.ru</email></contrib></contrib-group><pub-date pub-type="collection"><year>1994</year></pub-date><pub-date pub-type="epub"><day>15</day><month>04</month><year>1994</year></pub-date><volume>40</volume><issue>2</issue><issue-title>ТОМ 40, №2 (1994)</issue-title><fpage>82</fpage><lpage>85</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Вилтон П., Прайс Д.А., 1994</copyright-statement><copyright-year>1994</copyright-year><copyright-holder xml:lang="ru">Вилтон П., Прайс Д.А.</copyright-holder><copyright-holder xml:lang="en">Wilton P., Price D.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://www.probl-endojournals.ru/jour/article/view/11816">https://www.probl-endojournals.ru/jour/article/view/11816</self-uri><abstract><p>К 15 января 1992 г. в базу данных KIGS было включено 258 детей (отношение мальчиков к девочкам 1,5:1) с недостаточностью гормона роста (НГР), развившейся на фоне краниофарингиомы (КФ). Длительность лечения гормоном роста (ГР) варьировала от 0,2 до 15,4 года (в среднем 3,9 года). За 1338 лет лечения ГР (суммарно для всех больных) у 17 детей был рецидив КФ спустя 0,25—4,8 года (в среднем 2,3 года) от начала терапии ГР. Возраст в момент выявления опухоли, возраст и SDS для роста в начале лечения ГР, доза ГР, а также скорость роста до и в течение первого года лечения ГР не различались у больных с рецидивом и без такового. Частота рецидивов была также одинаковой у больных, которым проводилось одно хирургическое лечение, и у тех, у которых операция сочеталась с рентгенотерапией.</p></abstract><trans-abstract xml:lang="en"><p>By January 15, 1992, the KIGS database included 258 children (the ratio of boys to girls 1.5: 1) with growth hormone deficiency, which developed against the background of craniopharyngioma. The duration of growth hormone (GH) treatment ranged from 0.2 to 15.4 years (average 3.9 years). Over 1338 years of GH treatment (total for all patients), 17 children had a relapse of CF after 0.25-4.8 years (on average 2.3 years) from the start of GH treatment. The age at the time the tumor was detected, the age and SDS for growth at the beginning of GH treatment, the dose of GH, as well as the growth rate before and during the first year of GH treatment did not differ in patients with and without relapse. The recurrence rate was also the same in patients who underwent one surgical treatment, and in those in whom the operation was combined with radiotherapy.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>Краниофарингиома</kwd><kwd>Рецидив</kwd><kwd>Гормон роста</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Craniopharyngioma</kwd><kwd>Recurrence</kwd><kwd>Growth hormone</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">Sorva R., Heiskanen О. // Acta neurochir. 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