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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pharmateca</journal-id><journal-title-group><journal-title xml:lang="en">Pharmateca</journal-title><trans-title-group xml:lang="ru"><trans-title>Фарматека</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2073-4034</issn><issn publication-format="electronic">2414-9128</issn><publisher><publisher-name xml:lang="en">Bionika Media</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">289575</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">CHOICE OF THERAPEUTIC STRATEGY IN SEZARY SYNDROME: CASE REPORT</article-title><trans-title-group xml:lang="ru"><trans-title>Выбор терапевтической стратегии при синдроме Сезари: случай из практики</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zaslavsky</surname><given-names>D. V</given-names></name><name xml:lang="ru"><surname>Заславский</surname><given-names>Д. В</given-names></name></name-alternatives><bio xml:lang="en"><p>Department of dermatology</p></bio><bio xml:lang="ru"><p>Кафедра дерматовенерологии</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Yunovidova</surname><given-names>A. A</given-names></name><name xml:lang="ru"><surname>Юновидова</surname><given-names>А. А</given-names></name></name-alternatives><bio xml:lang="en"><p>Department of dermatology</p></bio><bio xml:lang="ru"><p>Кафедра дерматовенерологии</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Wolkenstein</surname><given-names>P.</given-names></name><name xml:lang="ru"><surname>Волькенштейн</surname><given-names>П.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Sydikov</surname><given-names>A. K</given-names></name><name xml:lang="ru"><surname>Сыдиков</surname><given-names>А. К</given-names></name></name-alternatives><bio xml:lang="en"><p>Department of dermatology</p></bio><bio xml:lang="ru"><p>Кафедра дерматовенерологии</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Skrek</surname><given-names>S. V</given-names></name><name xml:lang="ru"><surname>Скрек</surname><given-names>С. В</given-names></name></name-alternatives><bio xml:lang="en"><p>Teaching Assistant at the Department of Dermatovenerology</p></bio><bio xml:lang="ru"><p>ассистент кафедры дерматовенерологии</p></bio><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kovalchuk</surname><given-names>A. K</given-names></name><name xml:lang="ru"><surname>Ковальчук</surname><given-names>А. К</given-names></name></name-alternatives><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Sobolev</surname><given-names>A. V</given-names></name><name xml:lang="ru"><surname>Соболев</surname><given-names>А. В</given-names></name></name-alternatives><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Salogub</surname><given-names>G. N</given-names></name><name xml:lang="ru"><surname>Салогуб</surname><given-names>Г. Н</given-names></name></name-alternatives><bio xml:lang="en"><p>Department of Faculty Therapy with course of Endocrinology, Cardiology and Functional Diagnostics n.a. G.F. Lang with the Clinic</p></bio><bio xml:lang="ru"><p>кафедра факультетской терапии с курсом эндокринологии, кардиологии и функциональной диагностики им. Г.Ф. Ланга с клиникой</p></bio><xref ref-type="aff" rid="aff7"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">SPbSPMU</institution></aff><aff><institution xml:lang="ru">СПбГПМУ</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">NWSMU n.a. I.I. Mechnikov</institution></aff><aff><institution xml:lang="ru">СЗГМУ им. И.И. Мечникова</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Dermatology Service of the Henri Mondor University Hospital</institution></aff><aff><institution xml:lang="ru">Дерматологическая служба университетского госпиталя Энри Мондор</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">French Clinic of Skin Diseases n.a. Pierre Wolkenstein</institution></aff><aff><institution xml:lang="ru">Французская клиника кожных болезней Пьера Волькенштейна</institution></aff></aff-alternatives><aff-alternatives id="aff5"><aff><institution xml:lang="en">Dermatovenerologic Dispensary №11 of the Central District of St. Petersburg</institution></aff><aff><institution xml:lang="ru">Кожно-венерологический диспансер №11 Центрального района Санкт-Петербурга</institution></aff></aff-alternatives><aff-alternatives id="aff6"><aff><institution xml:lang="en">SRI of Medical Mycology n.a. P.N. Kashkin NWSMU .a. I.I. Mechnikov</institution></aff><aff><institution xml:lang="ru">НИИ медицинской микологии им. П.Н. Кашкина СЗГМУ им. И.И. Мечникова</institution></aff></aff-alternatives><aff-alternatives id="aff7"><aff><institution xml:lang="en">FSPbSMU n.a. Acad. I.P. Pavlov</institution></aff><aff><institution xml:lang="ru">ПСПГМУ им. акад. И.П. Павлова</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2016-10-20" publication-format="electronic"><day>20</day><month>10</month><year>2016</year></pub-date><volume>23</volume><issue>20</issue><issue-title xml:lang="en">NO20 (2016)</issue-title><issue-title xml:lang="ru">№20 (2016)</issue-title><fpage>53</fpage><lpage>58</lpage><history><date date-type="received" iso-8601-date="2023-02-26"><day>26</day><month>02</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2016, Bionika Media</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2016, ООО «Бионика Медиа»</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="en">Bionika Media</copyright-holder><copyright-holder xml:lang="ru">ООО «Бионика Медиа»</copyright-holder></permissions><self-uri xlink:href="https://journals.eco-vector.com/2073-4034/article/view/289575">https://journals.eco-vector.com/2073-4034/article/view/289575</self-uri><abstract xml:lang="en"><p>The article presents the modern concept of treatment of Sezary syndrome, discusses the choice of the optimal therapeutic algorithm; also own authors’ observation is provided. Sezary syndrome is a leukemic variant of epidermotropic T-cell skin lymphoma, which is clinically manifested by generalized erythema, macrolaminar desquamation and visceral pathology. This relatively rare dermatosis is characterized by often poor clinical response to treatment and poor prognosis without adequate treatment. Cases of complete recovery or long-term remission in patients with Sezary syndrome are rare casuistically A clinical case of Sezary syndrome in 52-year-old patient is described.</p></abstract><trans-abstract xml:lang="ru"><p>В статье представлена современная концепция лечения синдрома Сезари, обсуждается выбор оптимального терапевтического алгоритма, а также представлен случай собственного наблюдения. Синдром Сезари является лейкемическим вариантом Т- клеточной эпидермотропной лимфомы кожи, клинически проявляющийся покраснением всего кожного покрова, крупнопластинчатым шелушением и поражением внутренних органов. Этот относительно редкий дерматоз зачастую характеризуется слабым клиническим ответом на проводимую терапию и неблагоприятным прогнозом без адекватного лечения. Случаи полной реконвалесценции или длительной ремиссии у больных синдромом Сезари казуистически редки. Рассмотрен клинический случай синдрома Сезари у больного 52 лет.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Sezary syndrome</kwd><kwd>cutaneous T-cell lymphoma</kwd><kwd>phototherapy</kwd><kwd>rexinoids</kwd><kwd>bexarotene</kwd><kwd>RXR receptors</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>синдром Сезари</kwd><kwd>кожные Т-клеточные лимфомы</kwd><kwd>фототерапия</kwd><kwd>рексиноиды</kwd><kwd>бексаротен</kwd><kwd>RXR-рецепторы</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Scarisbrick J.J., Kim Y.H., Whittaker S.J., Wood G.S., Vermeer M.H., Prince H.M., Quagiino P. Prognostic factors, prognostic indices and staging in mycosis fungoides and Sézary syndrome: where are we now? Br. J. Dermatol. 2014;6:1226-36.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Whittaker S.J., Marsden J.R., Spittle M., Jones R.R. Joint British Association of Dermatologists and U.K. Cutaneous Lymphoma Group guidelines for the management of primary cutaneous T-cell lymphomas. Br. J. Dermatol. 2003; 149:1095-107.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Girardi M., Edelson R.L., Cutaneous T-Cell Lymphoma: Pathogenesis and Treatment. 0ncology.2000;14:1061-70.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Trautingera F., Knoblera R., Willemzeb R., Perisc K., Stadlerd R., Larochee L., D'incanf M., Rankig A., Pimpinellih N., Ortiz-Romeroi P., Dummerj R., Estrachk T., Whittakerl S. EORTC consensus recommendations for the treatment of mycosis fungoides/Sezary syndrome. Eur. J. Cancer. 2006;42:1014-30.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Olsen E.A., Rook A.H., Zic J., Kim Y., Porcu P., Querfeld C., Wood G., Demierre M.F., Pittelkow M., Wilson L.D., Pinter-Brown L., Advani R., Parker S., Kim E.J., Junkins-Hopkins J.M., Foss F., Cacchio P., Duvic M. Sézary syndrome: immunopathogenesis, literature review of therapeutic options, and recommendations for therapy by the United States Cutaneous Lymphoma Consortium (USCLC). J Am. Acad. Dermatol. 2011;64:352-404.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Stadler R., Kremer A. Therapeutic advances in cutaneous T-cell lymphoma (CTCL): from retinoids to rexinoids. Semin. Oncol. 2006; 33:7-10.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Ashworth J., Booker J., Breathnach S.M. Effects of topical corticosteroid therapy on Langerhans cell antigen presenting function in human skin. Br. J. Dermatol. 1988;118:457-70.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Herrmann J.J., Roenigk H.H. Jr., Honigsmann H. Ultraviolet radiation for treatment of cutaneous T-cell lymphoma. Hematol. Oncol. Clin. North Am.1995;9:1077-88.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Thomsen K., Hammar H., Molin L., Volden G. Retinoids plus PUVA (Re-PUVA) and PUVA in mycosis fungoides, plaque stage: a report from the Scandinavian mycosis fungoides group. Acta Derm. Venereol. 1989; 69:536-38.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Lowe N.J., Cripps D.J., Dufton P.A., Vickers C.F Photochemotherapy for mycosis fungoides: a clinical and histological study. Arch. Dermatol. 1979;115:50-3.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Mangelsdorf D.J., Umesono K., Evans R.M. The retinoid receptors. in: The Retinoids, Biology, Chemistry and Medicine. New York: Raven Press. 1994;2:319-50.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Farooqui A.A., Antony P., Ong W.Y., Horrocks L.A., Freysz L. Retinoic acid-mediated phospholipase A2 signaling in the nucleus. Brain Res. Rev. 2004;45:179-95.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Dunn L.K., Gaar L.R., Yentzer B.A., O'Neill J.L., Feldman S.R. Acitretin in dermatology: a review. J. Drugs Dermatol. 2011;10:772-82.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Cheeley J., Sahn R.E., DeLong L.K., Parker S.R. Acitretin for the treatment of cutaneous T-cell lymphoma. J. Am. Acad. Dermatol. 2013;68:247-54.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Sokoiowska-Wojdyto M., Lugowska-Umer H., Maciejewska-Radomska A. Oral retinoids and rexinoids in cutaneous T-cell lymphomas. Postepy Dermatol. Alergol. 2013;30:19-29.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Ларина С.Н., Чебышев Н.В., Ших Е.В., Каркищенко В.Н. Модулирование действия ядерных рецепторов и регуляция биотрансформации веществ. Биомедицина. 2009;1:70-80.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Beylot-Barry M. Bexarotène: Targretin. Ann. Dermatol. Venerol. 2007;134:987-91.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Bagot M., Bensussan A. Les lymphomes T épidermotropes comme modèles de progression tumorale. Med. Sci. 2006;22:192-96.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Bagot M. Les lymphomes cutanés. Paris: Springer, 2013. P 77-91.</mixed-citation></ref></ref-list></back></article>
