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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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">32</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2013-8-2-34-40</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>HEMATOLOGIC MALIGNANCIES: DIAGNOSIS, TREATMENT, SUPPORTIVE CARE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ГЕМОБЛАСТОЗЫ: ДИАГНОСТИКА, ЛЕЧЕНИЕ, СОПРОВОДИТЕЛЬНАЯ ТЕРАПИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Subcutaneous panniculitis-like T-cell lymphoma in children. Literature review and case reports</article-title><trans-title-group xml:lang="ru"><trans-title>Подкожная панникулит-подобная Т-клеточная лимфома у детей. Обзор литературы и описание случаев из практики</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Abramov</surname><given-names>D. S.</given-names></name><name xml:lang="ru"><surname>Абрамов</surname><given-names>Д. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Pathology Department</p></bio><bio xml:lang="ru"><p>Патологоанатомическое отделение</p></bio><email>abramovd_s@bk.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Konovalov</surname><given-names>D. M.</given-names></name><name xml:lang="ru"><surname>Коновалов</surname><given-names>Д. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Pathology Department</p></bio><bio xml:lang="ru"><p>Патологоанатомическое отделение</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Rogozhin</surname><given-names>D. V.</given-names></name><name xml:lang="ru"><surname>Рогожин</surname><given-names>Д. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Pathology Department</p><p>Pathology Department</p><p> </p></bio><bio xml:lang="ru"><p>Патологоанатомическое отделение</p><p>патологоанатомическое отделение</p><p> </p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Myakova</surname><given-names>N. V.</given-names></name><name xml:lang="ru"><surname>Мякова</surname><given-names>Н. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Oncohematology Department</p></bio><bio xml:lang="ru"><p>отделение онкогематологии</p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Biyachuev</surname><given-names>E. R.</given-names></name><name xml:lang="ru"><surname>Биячуев</surname><given-names>Э. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Adolescents and Young Adults Hematology/Oncology Department</p></bio><bio xml:lang="ru"><p>отделение гематологии/онкологии для подростков и молодых взрослых</p></bio><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Roshchin</surname><given-names>V. Yu.</given-names></name><name xml:lang="ru"><surname>Рощин</surname><given-names>В. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Pathology Department</p></bio><bio xml:lang="ru"><p>Патологоанатомическое отделение</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mitrofanova</surname><given-names>A. M.</given-names></name><name xml:lang="ru"><surname>Митрофанова</surname><given-names>А. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Pathology Department</p></bio><bio xml:lang="ru"><p>Патологоанатомическое отделение</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kislyakov</surname><given-names>A. N.</given-names></name><name xml:lang="ru"><surname>Кисляков</surname><given-names>А. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Pathology Department</p></bio><bio xml:lang="ru"><p>Патологоанатомическое отделение</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Federal Research Center of Hematology, Oncology and Immunology named after Dmitriy Rogachev,&#13;
Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Federal Research Center of Hematology, Oncology and Immunology named after Dmitriy Rogachev,&#13;
Ministry of Health of Russia&#13;
&#13;
Russian Children Clinical Hospital, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России&#13;
&#13;
ФГБУ «Российская детская клиническая больница» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Federal Research Center of Hematology, Oncology and Immunology named after Dmitriy Rogachev,&#13;
Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ ФНКЦ ДГОИ им. Дмитрия Рогачева Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Federal Research Center of Hematology, &#13;
Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ ФНКЦ ДГОИ им. Дмитрия Рогачева Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-05-22" publication-format="electronic"><day>22</day><month>05</month><year>2013</year></pub-date><volume>8</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>34</fpage><lpage>40</lpage><history><date date-type="received" iso-8601-date="2014-07-21"><day>21</day><month>07</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-07-21"><day>21</day><month>07</month><year>2014</year></date></history><permissions><copyright-year>2013</copyright-year><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/32">https://oncohematology.abvpress.ru/ongm/article/view/32</self-uri><abstract xml:lang="en"><p>Subcutaneous panniculitis-like T-cell lymphoma (SPTL) is a rare tumor from αβ mature cytotoxic T-lymphocytes, which primarily affects the subcutaneous adipose tissue and has morphological manifestations similar to panniculitis. SPTL frequency is less than 1 % of all NHL. It occurs in all age groups, but only 19–20 % are patients younger 20 years. Median age of patients is 35–36 years. To date are only a few cases in children described. In this article we described 3 SPTL cases in patients 1, 10 and 17 years old with typical clinical presentation and detailed analysis.</p></abstract><trans-abstract xml:lang="ru"><p>Подкожная панникулит-подобная Т-клеточная лимфома (ППТЛ) – редкая опухоль из зрелых цитотоксических αβ Т-лимфоцитов, которая первично поражает подкожную жировую ткань и имеет морфологические проявления, напоминающие панникулит. Частота ППТЛ составляет менее 1 % всех неходжкинских лимфом, встречается во всех возрастных группах, только 19–20 % составляют пациенты младше 20 лет, медиана возраста 35–36 лет. У детей описаны лишь единичные случаи. В данной статье представлены 3 случая ППТЛ у больных 1, 10 и 17 лет с типичным клиническим симптомокомплексом и подробным диагностическим анализом.</p></trans-abstract><kwd-group xml:lang="en"><kwd>subcutaneous panniculitis-like T-cell lymphoma</kwd><kwd>T-cell lymphoma immunophenotype</kwd><kwd>lymphoproliferative diseases in children</kwd><kwd>skin and subcutaneous adipose tissue lymphoma</kwd><kwd>panniculitis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>подкожная панникулит-подобная Т-клеточная лимфома</kwd><kwd>иммунофенотип Т-клеточной лимфомы</kwd><kwd>лимфопролиферативные заболевания у детей</kwd><kwd>лимфома кожи и подкожной жировой ткани</kwd><kwd>панникулит</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Jaffe E.S., Harris N.L., Vardiman J.W. et al. (еds.). Hematopathology. Elsevier Saunders Publishers, St. Louis, MO, USA 2010.</mixed-citation><mixed-citation xml:lang="ru">Jaffe E.S., Harris N.L., Vardiman J.W. et al. (еds.). Hematopathology. Elsevier Saunders Publishers, St. Louis, MO, USA 2010.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Swerdlow S.H., Campo E., Harris N.L. et al. WHO Classification of Tumours, Volume 2; IARC WHO Classification of Tumours, No 2. Lyon, France, IARC Press, 2008. 439 p.</mixed-citation><mixed-citation xml:lang="ru">Swerdlow S.H., Campo E., Harris N.L. et al. WHO Classification of Tumours, Volume 2; IARC WHO Classification of Tumours, No 2. Lyon, France, IARC Press, 2008. 439 p.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Hytiroglou P., Phelps R.G., Wattenberg D.J., Strauchen J.A. Histiocytic cytophagic panniculitis: molecular evidence for a clonal T-cell disorder. J Am Acad Dermatol 1992;27 (2 Pt 2):333–6.</mixed-citation><mixed-citation xml:lang="ru">Hytiroglou P., Phelps R.G., Wattenberg D.J., Strauchen J.A. Histiocytic cytophagic panniculitis: molecular evidence for a clonal T-cell disorder. J Am Acad Dermatol 1992;27 (2 Pt 2):333–6.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Willemze R., Jansen P.M., Cerroni L. et al. Subcutaneous panniculitis-like T-cell lymphoma: definition, classification, and prognostic factors: an EORTC Cutaneous Lymphoma Group Study of 83 cases. Blood 2008;111(2):838–45.</mixed-citation><mixed-citation xml:lang="ru">Willemze R., Jansen P.M., Cerroni L. et al. Subcutaneous panniculitis-like T-cell lymphoma: definition, classification, and prognostic factors: an EORTC Cutaneous Lymphoma Group Study of 83 cases. Blood 2008;111(2):838–45.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Parveen Z., Thompson K. Subcutaneous panniculitis-like T-cell lymphoma: redefinition of diagnostic criteria in the recent World Health Organization-European Organization for Research and Treatment of Cancer classification for cutaneous lymphomas. Arch Pathol Lab Med 2009Feb;133(2):303–8.</mixed-citation><mixed-citation xml:lang="ru">Parveen Z., Thompson K. Subcutaneous panniculitis-like T-cell lymphoma: redefinition of diagnostic criteria in the recent World Health Organization-European Organization for Research and Treatment of Cancer classification for cutaneous lymphomas. Arch Pathol Lab Med 2009Feb;133(2):303–8.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Mauch P.M., Armitage J.O., Coiffier B. et al. (eds.). Non-Hodgkin’s Lymphomas. Philadelphia, PA: Lippincott Williams &amp; Wilkins, 2004.</mixed-citation><mixed-citation xml:lang="ru">Mauch P.M., Armitage J.O., Coiffier B. et al. (eds.). Non-Hodgkin’s Lymphomas. Philadelphia, PA: Lippincott Williams &amp; Wilkins, 2004.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Cerroni L., Gatter K., Helmut K. Skin Lymphoma: The Illustrated Guide, 3rd Edition. Wiley-Blackwell, 2011. 288 p.</mixed-citation><mixed-citation xml:lang="ru">Cerroni L., Gatter K., Helmut K. Skin Lymphoma: The Illustrated Guide, 3rd Edition. Wiley-Blackwell, 2011. 288 p.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Gonzalez C.L., Medeiros L.J., Braziel R.M., Jaffe E.S. T-cell lymphoma inolving subcutaneous soft tissue. A clinicopathologic entity commonly associated with hemophagocytic syndrom. Am J Surg Pathol 1991;15(1):17–27.</mixed-citation><mixed-citation xml:lang="ru">Gonzalez C.L., Medeiros L.J., Braziel R.M., Jaffe E.S. T-cell lymphoma inolving subcutaneous soft tissue. A clinicopathologic entity commonly associated with hemophagocytic syndrom. Am J Surg Pathol 1991;15(1):17–27.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Hoque S.R., Child F.G., Whittaker S.G. et al. Subcutaneous panniculitis-like T-cell lymphoma: clinicopathological, immunophenotypic and molecular analysis of six patients. Br J Dermatol 2003;148: 516–25.</mixed-citation><mixed-citation xml:lang="ru">Hoque S.R., Child F.G., Whittaker S.G. et al. Subcutaneous panniculitis-like T-cell lymphoma: clinicopathological, immunophenotypic and molecular analysis of six patients. Br J Dermatol 2003;148: 516–25.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Burg G., Kempf W., Cozzio A. et al. WHO/EORTC classification of cutaneous lymphomas 2005: histological and molecular aspects. J Cutan Pathol 2005;32:647–74.</mixed-citation><mixed-citation xml:lang="ru">Burg G., Kempf W., Cozzio A. et al. WHO/EORTC classification of cutaneous lymphomas 2005: histological and molecular aspects. J Cutan Pathol 2005;32:647–74.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Hahtola S., Burghart Е., Jeskanen L. et al. Clinicopathological characterization and genomic aberration in subcutaneous panniculitis-like T-cell lymphoma. J Invest Dermatol 2008;128:2304–9.</mixed-citation><mixed-citation xml:lang="ru">Hahtola S., Burghart Е., Jeskanen L. et al. Clinicopathological characterization and genomic aberration in subcutaneous panniculitis-like T-cell lymphoma. J Invest Dermatol 2008;128:2304–9.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Willemze R., Dreyling M; ESMO Guidelines Working Group. Primary cutaneous lymphoma: ESMO clinical recommendations for diagnosis, treatment and follow-up. Ann Oncol 2009;20 (suppl 4):iv115-iv118.</mixed-citation><mixed-citation xml:lang="ru">Willemze R., Dreyling M; ESMO Guidelines Working Group. Primary cutaneous lymphoma: ESMO clinical recommendations for diagnosis, treatment and follow-up. Ann Oncol 2009;20 (suppl 4):iv115-iv118.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
