<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">detinf</journal-id><journal-title-group><journal-title xml:lang="ru">ДЕТСКИЕ ИНФЕКЦИИ</journal-title><trans-title-group xml:lang="en"><trans-title>CHILDREN INFECTIONS</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2072-8107</issn><issn pub-type="epub">2618-8139</issn><publisher><publisher-name>Association of Pediatricians and Infection Disease doctors</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.22627/2072-8107-2017-16-2-63-67</article-id><article-id custom-type="elpub" pub-id-type="custom">detinf-299</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>СЛУЧАЙ ИЗ ПРАКТИКИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CASE FROM PRACTICAL</subject></subj-group></article-categories><title-group><article-title>ИНФАНТИЛЬНЫЙ МИОФИБРОМАТОЗ У НОВОРОЖДЕННОГО</article-title><trans-title-group xml:lang="en"><trans-title>INFANTILE MIOFIBROMATOSIS IN NEWBORN: CASE REPORT</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>Бихерл</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Biherl</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"/><bio xml:lang="en"><p>Natalia V. Biherl, leading researcher, PhD</p></bio><email xlink:type="simple">mpsavenkov@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Савенкова</surname><given-names>М. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Savenkova</surname><given-names>M. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Савенкова Марина Сергеевна, главный научный сотрудник, д.м.н., профессор</p></bio><bio xml:lang="en"/><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ишутина</surname><given-names>Ю. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Ischutina</surname><given-names>Yu. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ишутина Юлия Леонидовна, заведущая отделением патологии новорожденных и недоношенных детей</p></bio><bio xml:lang="en"/><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шалатонин</surname><given-names>М. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Schalatonin</surname><given-names>M. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шалатонин Михаил Петрович, врач, патологоанатом</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Жилина</surname><given-names>С. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Gylina</surname><given-names>S. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Жилина Светлана Сергеевна, главный научный сотрудник, к.м.н.</p></bio><bio xml:lang="en"/><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Савлаев</surname><given-names>К. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Savlaev</surname><given-names>K. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Савлаев Казбек Фидарович, врач-онколог</p></bio><bio xml:lang="en"/><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Грицова</surname><given-names>Ю. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Gritsova</surname><given-names>Yu. V.</given-names></name></name-alternatives><bio xml:lang="en"/><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Научно-практический центр специализированной медицинской помощи детям им. Войно-Ясенецкого<country>Россия</country></aff><aff xml:lang="en">Scientific and Practical Center of Special Medical Care<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Морозовская детская гродская клиническая больница<country>Россия</country></aff><aff xml:lang="en">Morozovskaya Children's City Clinical Hospital<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru">Грицова Юлия Валерьевна, врач-неонатолог<country>Россия</country></aff><aff xml:lang="en">Scientific and Practical Center of Special Medical Care<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>04</day><month>07</month><year>2017</year></pub-date><volume>16</volume><issue>2</issue><fpage>63</fpage><lpage>67</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бихерл Н.В., Савенкова М.С., Ишутина Ю.Л., Шалатонин М.П., Жилина С.С., Савлаев К.Ф., Грицова Ю.В., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Бихерл Н.В., Савенкова М.С., Ишутина Ю.Л., Шалатонин М.П., Жилина С.С., Савлаев К.Ф., Грицова Ю.В.</copyright-holder><copyright-holder xml:lang="en">Biherl N.V., Savenkova M.S., Ischutina Y.L., Schalatonin M.P., Gylina S.S., Savlaev K.F., Gritsova Y.V.</copyright-holder><license 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://detinf.elpub.ru/jour/article/view/299">https://detinf.elpub.ru/jour/article/view/299</self-uri><abstract><p>В статье приводится описание клинического случая инфантильного миофиброматоза у новорожденного ребенка. Инфантильный миофиброматоз — редко встречающаяся мезенхимальная опухоль мягких тканей головы, конечности, туловища у детей, обладающая местным инфильтративным ростом без метастазов. В ходе обследования данного пациента были диагностированы множественные миофибромы, имевшие тенденцию к росту в сочетании с активной герпесвирусной инфекцией. В данном случае не исключается влияние смешанной герпетической инфекции на рост миофибром, так как на фоне противовирусного лечения была получена положительная динамика с уменьшением количества и размеров новообразований.</p></abstract><trans-abstract xml:lang="en"><p>The article describes the clinical case of infantile myofibromatosis of a newborn child. Infantile myofibromatosis is a rare mesenchymal tumor of the soft tissues of the head, limbs, trunk in children with infiltrative local growth, without metastases. During the examination the patient was diagnosed multiple myofibroms, which had a tendency to increase in the combination of active herpes infection. In this case, does not exclude the impact of mixed herpetic infection on the growth of myofibroms as on the background of antiviral treatment showed positive dynamics with a decrease in the number and size of tumors.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>инфатильный миофиброматоз</kwd><kwd>миофиброма</kwd><kwd>новорожденный</kwd><kwd>герпесвирусная инфекция</kwd></kwd-group><kwd-group xml:lang="en"><kwd>myofibromatosis</kwd><kwd>myofibroma</kwd><kwd>newborn</kwd><kwd>herpesvirus infection</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">Близнюков О.П., Смирнова Е.А., Пономарева М.В., Козлов Н.А. Инфантильная миофиброма (ИМ), гистологическое строение, ультраструктура, клиническое течение. Вопросы онкологии (СП). 2010; 56(4): 435—442. [Bliznyukov O.P., Smirnova E.A., Ponomareva M.V., Kozlov N.A. Infantile myofibroma (MI), histological structure, ultrastructure, clinical course. Oncology Questions (SP). 2010; 56 (4): 435—442. (In Russ.)]</mixed-citation><mixed-citation xml:lang="en">Близнюков О.П., Смирнова Е.А., Пономарева М.В., Козлов Н.А. Инфантильная миофиброма (ИМ), гистологическое строение, ультраструктура, клиническое течение. Вопросы онкологии (СП). 2010; 56(4): 435—442. [Bliznyukov O.P., Smirnova E.A., Ponomareva M.V., Kozlov N.A. Infantile myofibroma (MI), histological structure, ultrastructure, clinical course. Oncology Questions (SP). 2010; 56 (4): 435—442. (In Russ.)]</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Arts F.A., Chand D., Pecquet C., Velghe A.I., Constantinescu S., Hallberg B., Demoulin J.B. PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib. Oncogene. 2016 Jun 23; 35(25): 3239—48.</mixed-citation><mixed-citation xml:lang="en">Arts F.A., Chand D., Pecquet C., Velghe A.I., Constantinescu S., Hallberg B., Demoulin J.B. PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib. Oncogene. 2016 Jun 23; 35(25): 3239—48.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Cheung Y.H., Gayden T., Campeau P.M., LeDuc C.A. et al. A recurrent PDGFRB mutation causes familial infantile myofibromatosis. Am J Hum Genet. 2013 Jun 6; 92(6): 996—1000. doi: 10.1016/j.ajhg. 2013.04.026.</mixed-citation><mixed-citation xml:lang="en">Cheung Y.H., Gayden T., Campeau P.M., LeDuc C.A. et al. A recurrent PDGFRB mutation causes familial infantile myofibromatosis. Am J Hum Genet. 2013 Jun 6; 92(6): 996—1000. doi: 10.1016/j.ajhg. 2013.04.026.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Martignetti J.A., Tian L., Li D., Ramirez M.C., Camacho-Vanegas O. et al. Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. Am J Hum Genet. 2013 Jun 6; 92(6): 1001—7. doi: 10.1016/j.ajhg.2013.04.024.</mixed-citation><mixed-citation xml:lang="en">Martignetti J.A., Tian L., Li D., Ramirez M.C., Camacho-Vanegas O. et al. Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. Am J Hum Genet. 2013 Jun 6; 92(6): 1001—7. doi: 10.1016/j.ajhg.2013.04.024.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Levine E., Freneaux P., Schleiermacher G., Brisse H., Pannier S., Teissier N., Mesples B., Orbach D. Risk-adapted therapy for infantile myofibromatosis in children. Pediatr Blood Cancer. 2012 Jul 15; 59(1): 115—20. doi: 10.1002/pbc.23387.</mixed-citation><mixed-citation xml:lang="en">Levine E., Freneaux P., Schleiermacher G., Brisse H., Pannier S., Teissier N., Mesples B., Orbach D. Risk-adapted therapy for infantile myofibromatosis in children. Pediatr Blood Cancer. 2012 Jul 15; 59(1): 115—20. doi: 10.1002/pbc.23387.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Wu W., Chen J., Cao X., Yang M., Zhu J., Zhao G. Solitary infantile myofibromatosis in the bones of the upper extremities: Two rare cases and a review of the literature. Oncol Lett. 2013 Nov; 6(5): 1406— 1408.</mixed-citation><mixed-citation xml:lang="en">Wu W., Chen J., Cao X., Yang M., Zhu J., Zhao G. Solitary infantile myofibromatosis in the bones of the upper extremities: Two rare cases and a review of the literature. Oncol Lett. 2013 Nov; 6(5): 1406— 1408.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Weaver M.S., Navid F., Huppmann A., Meany H., Angiolillo A. Vincristine and Dactinomycin in Infantile Myofibromatosis With a Review of Treatment Options. J Pediatr Hematol Oncol. 2015 Apr; 37(3): 237—41. 8. Wu S.Y., McCavit T.L., Cederberg K., Galindo R.L., Leavey P.J. Chemotherapy for Generalized Infantile Myofibromatosis With Visceral Involvement. J Pediatr Hematol Oncol. 2015 Jul; 37(5): 402—5. doi: 10.1097/MPH.0000000000000132.</mixed-citation><mixed-citation xml:lang="en">Weaver M.S., Navid F., Huppmann A., Meany H., Angiolillo A. Vincristine and Dactinomycin in Infantile Myofibromatosis With a Review of Treatment Options. J Pediatr Hematol Oncol. 2015 Apr; 37(3): 237—41. 8. Wu S.Y., McCavit T.L., Cederberg K., Galindo R.L., Leavey P.J. Chemotherapy for Generalized Infantile Myofibromatosis With Visceral Involvement. J Pediatr Hematol Oncol. 2015 Jul; 37(5): 402—5. doi: 10.1097/MPH.0000000000000132.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
