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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">pmj</journal-id><journal-title-group><journal-title xml:lang="ru">Тихоокеанский медицинский журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Pacific Medical Journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1609-1175</issn><publisher><publisher-name>TGMU</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.34215/1609-1175-2024-1-69-71</article-id><article-id custom-type="elpub" pub-id-type="custom">pmj-2693</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>НАБЛЮДЕНИЯ ИЗ ПРАКТИКИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PRACTICE OBSERVATIONS</subject></subj-group></article-categories><title-group><article-title>Редкий случай аномалии развития яичек у подростка 17 лет</article-title><trans-title-group xml:lang="en"><trans-title>Rare case of testicular abnormality in a 17-year-old adolescent boy</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>Панчоян</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Panchoyan</surname><given-names>V. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Владивосток </p></bio><bio xml:lang="en"><p>Vladivostok</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Белякова</surname><given-names>О. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Belyakova</surname><given-names>O. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Владивосток</p></bio><bio xml:lang="en"><p>Vladivostok</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/0000-0001-5325-2891</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Белов</surname><given-names>С. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Belov</surname><given-names>S. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Белов Сергей Анатольевич – к.м.н., торакальный хирург </p><p>690950, г. Владивосток, о. Русский. пос. Аякс, 10, кор. 25 </p></bio><bio xml:lang="en"><p>Sergey A. Belov, Cand. Sci. (Med.), thoracic surgeon </p><p>10, build. 25 Ajax settlement, Russkiy Island, Vladivostok, 690950 </p></bio><email xlink:type="simple">sur_belove@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Краевой клинический центр специализированных видов медицинской помощи</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Regional Clinical Center for Specialized Types of Medical Care</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Медицинский комплекс Дальневосточного федерального университета</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Far Eastern Federal University – Medical Complex</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>18</day><month>05</month><year>2024</year></pub-date><volume>0</volume><issue>1</issue><fpage>69</fpage><lpage>71</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Панчоян В.М., Белякова О.О., Белов С.А., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Панчоян В.М., Белякова О.О., Белов С.А.</copyright-holder><copyright-holder xml:lang="en">Panchoyan V.M., Belyakova O.O., Belov S.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.tmj-vgmu.ru/jour/article/view/2693">https://www.tmj-vgmu.ru/jour/article/view/2693</self-uri><abstract><p>Полиорхизм является редкой врожденной аномалией, определяемой как наличие более двух яичек. Эта патология чрезвычайно редка и может длительно оставаться бессимптомной. Заболевание обнаруживается преимущественно при исследовании другой урологической патологии, такой как воспаление, гидроцеле, перекручивание сосудов яичка, паховой грыжи, мужского бесплодия, а также злокачественного перерождения. Мы сообщаем о случае полиорхизма, подтвержденного во время операции по поводу перекрута гидатиды левого яичка у 17-летнего мальчика. Нештатное яичко имело собственную влагалищную оболочку, придаток яичка, общий семявыносящий проток и совместное кровоснабжение с левым яичком. При вмешательстве семенники сохранили. Нарушение сперматогенеза у пациента не выявили.</p></abstract><trans-abstract xml:lang="en"><p>Polyorchism is a rare congenital anomaly defined as the incidence of more than two testicles. This pathology is considered to be extremely rare and may remain asymptomatic for a long time. The disease is detected predominantly during the examination of other urologic pathologies such as inflammation, hydrocele, testicular torsion, inguinal hernia, male infertility, and malignant changes. The reported case of polyorchism was confirmed during surgery for left testicular hydatid torsion in a 17-yearold boy. The abnormal testis had its own tunica vaginalis testis, epididymis, common deferent duct, and shared blood supply with the left testis. The testes were preserved during surgery. No impaired spermatogenesis was detected in the patient.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>детская хирургия</kwd><kwd>аномалия яичек</kwd><kwd>полиорхизм</kwd></kwd-group><kwd-group xml:lang="en"><kwd>pediatric surgery</kwd><kwd>testicular abnormality</kwd><kwd>poliorchism</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">Колесников Г.С. Полиорхизм. 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