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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">surgumed</journal-id><journal-title-group><journal-title xml:lang="ru">Вестник СурГУ. Медицина</journal-title><trans-title-group xml:lang="en"><trans-title>Vestnik SurGU. Meditsina</trans-title></trans-title-group></journal-title-group><issn pub-type="epub">2949-3447</issn><publisher><publisher-name>Сургутский государственный университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.34822/2304-9448-2022-2-65-68</article-id><article-id custom-type="elpub" pub-id-type="custom">surgumed-530</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>КЛИНИЧЕСКАЯ МЕДИЦИНА. КЛИНИЧЕСКИЙ СЛУЧАЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL MEDICINE. CLINICAL CASE</subject></subj-group></article-categories><title-group><article-title>КЛИНИЧЕСКИЙ СЛУЧАЙ ЧИСТОЙ ДИСГЕНЕЗИИ ГОНАД – СИНДРОМА СВАЙЕРА</article-title><trans-title-group xml:lang="en"><trans-title>CLINICAL CASE OF PURE GONADAL DYSGENESIS – SWYER SYNDROME</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4851-7503</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Верховых</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Verkhovykh</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>аспирант</p><p>E-mail: verkhovikh_ev@edu.surgu.ru</p></bio><bio xml:lang="en"><p>PostgraduateE-mail: verkhovikh_ev@edu.surgu.ru</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/0000-0003-0283-2428</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гирш</surname><given-names>Я. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Girsh</surname><given-names>Ya. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>доктор медицинских наукE-mail: prof.girsh@yandex.ru</p></bio><bio xml:lang="en"><p>Doctor of Sciences (Medicine)</p><p>E-mail: prof.girsh@yandex.ru</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/0000-0002-2000-7694</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Калинченко</surname><given-names>Н. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Kalinchenko</surname><given-names>N. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кандидат медицинских наук</p><p>E-mail: kalinnat@rambler.ru</p></bio><bio xml:lang="en"><p>Candidate of Sciences (Medicine)</p><p>E-mail: kalinnat@rambler.ru</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Сургутский государственный университет, Сургут</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Surgut State University, Surgut</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Национальный медицинский исследовательский центр эндокринологии</institution><country>Россия</country></aff><aff xml:lang="en"><institution>The National Medical Research Center for Endocrinology, Moscow</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>24</day><month>06</month><year>2022</year></pub-date><volume>0</volume><issue>2 (52)</issue><fpage>65</fpage><lpage>68</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Верховых Е.В., Гирш Я.В., Калинченко Н.Ю., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Верховых Е.В., Гирш Я.В., Калинченко Н.Ю.</copyright-holder><copyright-holder xml:lang="en">Verkhovykh E.V., Girsh Y.V., Kalinchenko N.Y.</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.surgumed.ru/jour/article/view/530">https://www.surgumed.ru/jour/article/view/530</self-uri><abstract><p>Цель – представить клинический случай чистой дисгенезии гонад у пациентки. Материалы и методы. Представлен клинический случай синдрома Свайера у девушки 16 лет, проанализированы анамнестические и клинические данные, результаты лабораторных и инструментальных обследований, постоперационные результаты и эффект заместительной гормональной терапии. Результаты. В процессе обследования подростка с женским фенотипом, высокорослостью и первичной аменореей выявлено повышение гонадотропинов и гипоплазия матки. При цитогенетическом исследовании установлен кариотип 46, ХУ. Проведено лапароскопическое удаление двусторонних гонадобластом с последующим подбором заместительной гормональной терапии.</p></abstract><trans-abstract xml:lang="en"><p>The study aims to present a clinical case of pure gonadal dysgenesis in a female patient. Materials and methods. A clinical case of Swyer syndrome in a 16-year-old girl is presented. The anamnestic and clinical data, the results of laboratory and instrumental examinations, postoperative results and the effect of hormone replacement therapy were analyzed. Results. During the examination of a teenager with a female phenotype, tall stature and primary amenorrhea, an increase in gonadotropins and uterine hypoplasia were recorded. Cytogenetic examination revealed a 46,XY karyotype. Laparoscopic removal of bilateral gonadoblastoma was performed, followed by the selection of hormone replacement therapy.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>синдром Свайера</kwd><kwd>нарушение формирования пола</kwd><kwd>чистая дисгенезия гонад</kwd><kwd>гонадобластома</kwd><kwd>аменорея</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Swyer syndrome</kwd><kwd>violation of sex formation</kwd><kwd>pure gonadal dysgenesis</kwd><kwd>gonadoblastoma</kwd><kwd>amenorrhea</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">Coutin A. S., Hamy A., Fondevilla M., Savigny B., Paineau J., Visset J. Pure 46,XY Gonadal Dysgenesis // J Gynecol Obstet Biol Reprod. 1996. Vol. 25, Is. 8. Р. 792–796.</mixed-citation><mixed-citation xml:lang="en">Coutin A. S., Hamy A., Fondevilla M., Savigny B., Paineau J., Visset J. 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