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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">endoserg</journal-id><journal-title-group><journal-title xml:lang="ru">Эндокринная хирургия</journal-title><trans-title-group xml:lang="en"><trans-title>Endocrine Surgery</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2306-3513</issn><issn pub-type="epub">2310-3965</issn><publisher><publisher-name>Типография «Печатных дел Мастер»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/serg12771</article-id><article-id custom-type="elpub" pub-id-type="custom">endoserg-12771</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>Клинический случай</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Clinical Case</subject></subj-group></article-categories><title-group><article-title>Феохромоцитома, осложненная паранеопластическим синдромом в виде миелодиспластической трехростковой цитопении</article-title><trans-title-group xml:lang="en"><trans-title>Pheochromocytoma with paraneoplastic phenomena manifested as myelodysplastic 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/0000-0001-6694-9030</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сергийко</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Sergiiko</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Сергийко Сергей Владимирович, д.м.н., доцент</p><p>eLibrary SPIN: 5558-1362</p><p>Челябинск</p></bio><bio xml:lang="en"><p>Sergei V. Sergiiko, MD, Dr. Sci. (Med.), Associate professor</p><p>eLibrary SPIN: 5558-1362</p><p>Chelyabinsk</p></bio><email xlink:type="simple">ssv_1964@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/0000-0003-2198-4793</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коротовский</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Korotovsky</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Коротовский Денис Владимирович, врач-хирург</p><p>eLibrary SPIN: 8004-6158</p><p>454092, г. Челябинск, ул. Воровского, д. 16, корп. 3</p></bio><bio xml:lang="en"><p>Denis V. Korotovskii, MD, surgeon</p><p>eLibrary SPIN: 8004-6158</p><p>Vorovskogo str. 16, Chelyabinsk, 454092</p></bio><email xlink:type="simple">korotovskymd@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тюльганова</surname><given-names>В. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Tul`ganova</surname><given-names>V. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тюльганова Валерия Леонидовна, к.м.н.</p><p>Челябинск</p></bio><bio xml:lang="en"><p>Valeria L. Tul`ganova, MD, Cand. Sci. (Med.)</p><p>Chelyabinsk</p></bio><email xlink:type="simple">val_tu@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ломова</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Lomova</surname><given-names>I. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ломова Ирина Викторовна, врач-эндокринолог</p><p>eLibrary SPIN: 5896-6768</p><p>Челябинск</p></bio><bio xml:lang="en"><p>Irina V. Lomova, MD</p><p>eLibrary SPIN: 5896-6768</p><p>Chelyabinsk</p></bio><email xlink:type="simple">lomira20@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Буторин</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Butorin</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Буторин Александр Сергеевич, к.м.н.</p><p>Челябинск</p></bio><bio xml:lang="en"><p>Alexander S. Butorin, MD, Cand. Sci. (Med.)</p><p>Chelyabinsk</p></bio><email xlink:type="simple">asbutorin@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Южно-Уральский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>South-Ural State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Городская клиническая больница №1</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chelyabinsk city clinical hospital №1</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ГБУЗ ЧОКБ</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chelyabinsk regional clinical hospital</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>19</day><month>01</month><year>2023</year></pub-date><volume>16</volume><issue>1</issue><fpage>23</fpage><lpage>28</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Сергийко С.В., Коротовский Д.В., Тюльганова В.Л., Ломова И.В., Буторин А.С., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Сергийко С.В., Коротовский Д.В., Тюльганова В.Л., Ломова И.В., Буторин А.С.</copyright-holder><copyright-holder xml:lang="en">Sergiiko S.V., Korotovsky D.V., Tul`ganova V.L., Lomova I.V., Butorin A.S.</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.surg-endojournals.ru/jour/article/view/12771">https://www.surg-endojournals.ru/jour/article/view/12771</self-uri><abstract><p>Представлен клинический случай течения заболевания у пациента 22 лет с феохромоцитомой левого надпочечника, осложненной развитием паранеопластического синдрома в виде миелодиспластического синдрома. Дебют заболевания сопровождался классической клинической картиной, характерной для феохромоцитомы. По данным мультиспиральной компьютерной томографии брюшной полости выявлена больших размеров опухоль левого надпочечника. В результате лабораторного обследования подтверждены высокая концентрация катехоламинов мочи, а  также тяжелая анемия и тромбоцитопения. Пациент консультирован гематологом, проведена стернальная пункция с иммунофенотипированием, диагностирован вторичный гипопластический синдром неуточненной этиологии. После длительной предоперационной медикаментозной подготовки α-адреноблокаторами, коррекции анемии и  тромбоцитопении выполнена хирургическая операция — торакофренолапаротомия, левосторонняя адреналэктомия, спленэктомия. Гистологическое заключение после операции: зрелая феохромоцитома с расстройством кровообращения; морфологические изменения селезенки, характерные для анемии.</p><p>В раннем послеоперационном периоде пациенту проводились заместительная терапия надпочечниковой недостаточности, плазмогемотрансфузии и инфузии тромбоконцентрата с целью коррекции анемии и тромбоцитопении. В позднем послеоперационном периоде сохранялись явления анемии и тромбоцитопении без проявлений геморрагического синдрома. Миелодиспластический синдром по типу рефрактерной анемии и тромбоцитопении тяжелой степени сохранялся в течение длительного периода времени и требовал периодической коррекции. Лишь спустя 5 лет после хирургического удаления феохромоцитомы у пациента наметилась тенденция к нормализации показателей крови и нивелированию лабораторных признаков миелодиспластического синдрома.</p></abstract><trans-abstract xml:lang="en"><p>We present a clinical case of 22yo patient with diagnosis of pheochoromocytoma complicated with myelodysplastic syndrome as manifestation of paraneoplastic phenomenon. The onset of the disease displays typical clinical picture of pheochromacytoma. After medical examination and survey it was discovered a tumor in left adrenal gland and elevation of metanephrines and normetanephrines. In addition, patient has severe anemia and thrombocytopenia. Sternal punction with morphological examination and immunophenotyping were performed. Patient had consulted by hematologist. After all additional analysis cause of anemia and thrombocytopenia remained unknown and related to presence of tumor.</p><p>Patient was performed a long-time and vast pre-operative preparation with administration of doxazosin and transfusions of blood and platelet concentrate. In continuation, mass in left adrenal gland was excised with spleen by thoracophrenolaparotomy. Morphology confirmed pheochromacytoma, which has typical histological structure and circulatory disorders. Spleen has no specifical features except of focuses of extramedullar hematopoiesis. Patient has short period of hormone therapy to avoid adrenal crisis on post-operative stage. Also massive transfutions of blood and platelet concentrate was performed due to persisting anemia and thrombocytopenia. There were no manifestations of hemorrhage syndrome after the surgery. Myelodysplastic syndrome was detected 3 month later and manifested itself in form of refractory anemia and severe thrombocytopenia, which persisted for long period and required corrections with therapy and transfusions. Only through 5-year observation after adrenalectomy patient has positive dynamic and leveling of laboratory tests without symptoms of myelodysplastic syndrome.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>феохромоцитома</kwd><kwd>паранеопластический синдром</kwd><kwd>миелодиспластический синдром</kwd></kwd-group><kwd-group xml:lang="en"><kwd>pheochromocytoma</kwd><kwd>paraneoplastic syndromes</kwd><kwd>myelodysplastic syndromes</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">Платонова Н.М., Юкина М.Ю., Молашенко Н.В., и др. Феохромоцитома / В кн.: Трошина Е.А., ред. 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