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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">bloodjour</journal-id><journal-title-group><journal-title xml:lang="ru">Гематология и трансфузиология</journal-title><trans-title-group xml:lang="en"><trans-title>Russian journal of hematology and transfusiology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0234-5730</issn><issn pub-type="epub">2411-3042</issn><publisher><publisher-name>ООО Издательский дом «Практика»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.35754/0234-5730-2019-64-3-353-361</article-id><article-id custom-type="elpub" pub-id-type="custom">bloodjour-153</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>КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CASE REPORTS</subject></subj-group></article-categories><title-group><article-title>ТЕРАПИЯ РЕЗИСТЕНТНЫХ ФОРМ ПОДКОЖНОЙ ПАННИКУЛИТОПОДОБНОЙ Т-КЛЕТОЧНОЙ ЛИМФОМЫ</article-title><trans-title-group xml:lang="en"><trans-title>THERAPY OF THE RESISTANT FORMS OF SUBCUTANEOUS PANNICULITIS-LIKE T-CELL LYMPHOMA</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3967-9183</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Горенкова</surname><given-names>Л. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Gorenkova</surname><given-names>L. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кандидат медицинских наук, научный сотрудник отделения интенсивной высокодозной химиотерапии гемобластозов с круглосуточным стационаром,</p><p>125167, г. Москва, Новый Зыковский проезд, 4</p></bio><bio xml:lang="en"><p>Cand. Sci. (Med.), Researcher, Department of Intensive High-Dose Chemotherapy for Hemoblastoses,</p><p>125167, Moscow, Novyy Zykovskiy proezd, 4</p></bio><email xlink:type="simple">l.aitova@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/0000-0002-7721-2074</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кравченко</surname><given-names>С. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Kravchenko</surname><given-names>S. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кандидат медицинских наук, доцент, заведующий отделением интенсивной высокодозной химиотерапии гемобластозов с круглосуточным стационаром,</p><p>125167, г. Москва, Новый Зыковский проезд, 4</p></bio><bio xml:lang="en"><p>Cand. Sci. (Med.), Head of the Department of Intensive High-Dose Chemotherapy for Hemoblastoses, </p><p>125167, Moscow, Novyy Zykovskiy proezd, 4</p></bio><email xlink:type="simple">kravchenko.s@blood.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/0000-0002-4937-018X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Силаев</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Silaev</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кандидат медицинских наук, врач-хирург научно-клинического отделения гематологической хирургии,</p><p>125167, г. Москва, Новый Зыковский проезд, 4</p></bio><bio xml:lang="en"><p>Cand. Sci. (Med.), Surgeon, Scientific and Clinical Department of Hematological Surgery, </p><p>125167, Moscow, Novyy Zykovskiy proezd, 4</p></bio><email xlink:type="simple">silaev.m@blood.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/0000-0003-2424-9524</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рыжикова</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Ryzhikova</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>научный сотрудник лаборатории молекулярной гематологии,</p><p>125167, г. Москва, Новый Зыковский проезд, 4</p></bio><bio xml:lang="en"><p>Researcher, Laboratory of Molecular Haematology,</p><p>125167, Moscow, Novyy Zykovskiy proezd, 4</p></bio><email xlink:type="simple">ryzhykova.n@blood.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр гематологии» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Research Center for Hematology</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>09</day><month>11</month><year>2019</year></pub-date><volume>64</volume><issue>3</issue><fpage>353</fpage><lpage>361</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Горенкова Л.Г., Кравченко С.К., Силаев М.А., Рыжикова Н.В., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Горенкова Л.Г., Кравченко С.К., Силаев М.А., Рыжикова Н.В.</copyright-holder><copyright-holder xml:lang="en">Gorenkova L.G., Kravchenko S.K., Silaev M.A., Ryzhikova N.V.</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.htjournal.ru/jour/article/view/153">https://www.htjournal.ru/jour/article/view/153</self-uri><abstract><sec><title>Введение</title><p>Введение. Подкожная панникулитоподобная Т-клеточная лимфома (ППТКЛ) относится к редкой группе кожных лимфопролиферативных заболеваний с клиническими проявлениями, напоминающими панникулит, α/β-цитотоксическим иммунофенотипом опухолевых клеток и разнонаправленным течением: от индолентных до агрессивных форм.</p><p>Цель работы — описать больных ППТКЛ с агрессивным клиническим течением заболевания и рефрактерностью к нескольким линиям химиотерапии.</p></sec><sec><title>Результаты</title><p>Результаты. Представлены два клинических наблюдения больных с генерализованным характером поражения и наличием факторов неблагоприятного прогноза, у которых достигнуты полные продолжительные ремиссии заболевания в результате применения курсов химиотерапии с включением гемцитабина.</p></sec><sec><title>Заключение</title><p>Заключение: несмотря на то, что у обоих больных ППТКЛ наблюдалась рефрактерность как минимум к трем видам лечения, использование гемцитабина позволило достигнуть длительных полных ремиссий заболевания. </p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) belongs to a rare group of skin lymphoproliferative disorders, which is characterised by panniculitis-like clinical manifestations, the α/β cytotoxic immunophenotype of tumour cells, as well as a multidirectional course from indolent to aggressive forms.</p></sec><sec><title>Aim</title><p>Aim. To examine patients with SPTCL having an aggressive clinical course and characterised by refractoriness to several lines of chemotherapy.</p></sec><sec><title>Results</title><p>Results. We present two case reports of patients with a generalised lesions and unfavourable prognostic factors, who achieved complete long-term remission of the disease as a result of gemcitabine chemotherapy.</p></sec><sec><title>Conclusion</title><p>Conclusion. Despite the fact that both observed SPTCL patients demonstrated refractoriness to at least three types of treatment, the use of gemcitabine allowed long-term complete remissions of the disease to be achieved. </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>подкожная панникулитоподобная Т-клеточная лимфома</kwd><kwd>лимфома кожи</kwd><kwd>ремиссия заболевания</kwd><kwd>волчаночный панникулит</kwd><kwd>гемцитабин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>subcutaneous panniculitis-like T-cell lymphoma</kwd><kwd>skin lymphoma</kwd><kwd>disease remission</kwd><kwd>lupus panniculitis</kwd><kwd>gemcitabine</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">Gonzalez C.L., Medeiros L.J., Braziiel R.M., Jaffe E.S. T-cell lymphoma involving subcutaneous tissue: a clinicopathologic entity commonly associated with hemophagocytic syndrome. 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