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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">r-n-j</journal-id><journal-title-group><journal-title xml:lang="ru">Российский неврологический журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Russian neurological journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2658-7947</issn><issn pub-type="epub">2686-7192</issn><publisher><publisher-name>МИА</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.30629/2658-7947-2024-29-2-66-70</article-id><article-id custom-type="elpub" pub-id-type="custom">r-n-j-555</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>ИССЛЕДОВАНИЯ И КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL RESEARCHES AND CASE REPORTS</subject></subj-group></article-categories><title-group><article-title>Шваннома коленчатого узла</article-title><trans-title-group xml:lang="en"><trans-title>Clinical case of genous schwannoma</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0002-8783-0148</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Акопян</surname><given-names>Н. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Akopyan</surname><given-names>N. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ставрополь</p></bio><bio xml:lang="en"><p>Stavropol</p></bio><email xlink:type="simple">inarcho@mail.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/0009-0005-0529-1948</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Костерина</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kosterina</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ставрополь</p></bio><bio xml:lang="en"><p>Stavropol</p></bio><email xlink:type="simple">kosteliza00@mail.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/0000-0002-4084-3307</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Раевская</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Raevskaya</surname><given-names>A. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ставрополь</p></bio><bio xml:lang="en"><p>Stavropol</p></bio><email xlink:type="simple">nastya_raevskaya96@mail.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/0009-0008-5958-1723</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Дерябин</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Deryabin</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ставрополь</p></bio><bio xml:lang="en"><p>Stavropol</p></bio><email xlink:type="simple">jump.555@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/0000-0001-9187-8481</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Вышлова</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Vyshlova</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ставрополь</p></bio><bio xml:lang="en"><p>Stavropol</p></bio><email xlink:type="simple">irisha2801@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/0000-0003-1472-6024</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Карпов</surname><given-names>С. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Karpov</surname><given-names>S. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ставрополь</p></bio><bio xml:lang="en"><p>Stavropol</p></bio><email xlink:type="simple">karpov25@rambler.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Ставропольский государственный медицинский университет<country>Россия</country></aff><aff xml:lang="en">Stavropol State Medical University<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>24</day><month>05</month><year>2024</year></pub-date><volume>29</volume><issue>2</issue><fpage>66</fpage><lpage>70</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Акопян Н.Б., Костерина Е.А., Раевская А.И., Дерябин А.С., Вышлова И.А., Карпов С.М., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Акопян Н.Б., Костерина Е.А., Раевская А.И., Дерябин А.С., Вышлова И.А., Карпов С.М.</copyright-holder><copyright-holder xml:lang="en">Akopyan N.B., Kosterina E.A., Raevskaya A.I., Deryabin A.S., Vyshlova I.A., Karpov S.M.</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://www.r-n-j.com/jour/article/view/555">https://www.r-n-j.com/jour/article/view/555</self-uri><abstract><p>Шванномы — это доброкачественные опухоли, которые возникают из шванновских клеток и составляют примерно 5% всех доброкачественных опухолей мягких тканей, характеризуются медленным ростом (1–2 мм в год) и клинически бессимптомны на протяжении длительного времени.</p><sec><title>Материал и методы</title><p>Материал и методы. Проведен обзор источников литературы за 2000–2023 гг., использованы источники российской научной электронной библиотеки eLIBRARY, PubMed. Представлено клиническое наблюдение пациента с шванномой коленчатого узла.</p></sec><sec><title>Результаты</title><p>Результаты. Шванномы могут возникать в любом возрасте, не выявлено гендерных особенностей, чаще пик заболеваемости приходится на период между третьей и шестой декадами жизни. Отмечается связь с генетическими нарушениями, в частности при нейрофиброматозе. Доминирующими методами диагностики остаются магнитно-резонансная томография и мультиспиральная компьютерная томография головного мозга.</p></sec><sec><title>Заключение</title><p>Заключение. Представленный клинический случай демонстрирует длительное, малосимптомное течение шванномы коленчатого узла с интракраниальным распространением. Проведенное хирургическое лечение способствовало улучшению качества жизни пациента.</p></sec></abstract><trans-abstract xml:lang="en"><p>Schwannomas are benign tumors that arise from Schwann cells and account for approximately 5% of all benign soft tissue tumors, are characterized by slow growth (1–2 mm per year) and are clinically asymptomatic for a long time.</p><sec><title>Material and methods</title><p>Material and methods. A review of literary sources for 2000–2023 was carried out, sources from the Russian scientific electronic library eLIBRARY, RSCI databases, and PubMed were used. A clinical case of patient with geniculate ganglion schwannoma is presented.</p></sec><sec><title>Results</title><p>Results. Schwannomas can occur at any age, no gender specific characteristics have been identified, the incidence most often occurs between the third and sixth decades, and there is an association with genetic disorders, in particular with neurofibromatosis. The dominant diagnostic methods remain MRI and MSCT of the brain.</p></sec><sec><title>Conclusion</title><p>Conclusion. The presented clinical case demonstrates a long-term, asymptomatic course of geniculate ganglion schwannoma with intracranial spread. The surgical treatment contributed to improving the patient’s quality of life.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>невринома</kwd><kwd>неврилеммома</kwd><kwd>новообразование лицевого нерва</kwd><kwd>шваннома коленчатого узла</kwd></kwd-group><kwd-group xml:lang="en"><kwd>neurinoma</kwd><kwd>neurilemmoma</kwd><kwd>facial nerve neoplasm</kwd><kwd>cranial node schwannoma</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">Bartindale M, Heiferman J, Joyce C, Balasubramanian N, Anderson D, Leonetti J. The Natural History of Facial Schwannomas: A Meta-Analysis of Case Series. 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