<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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">Bone and soft tissue sarcomas, tumors of the skin</journal-id><journal-title-group><journal-title xml:lang="en">Bone and soft tissue sarcomas, tumors of the skin</journal-title><trans-title-group xml:lang="ru"><trans-title>Саркомы костей, мягких тканей и опухоли кожи</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2219-4614</issn><issn publication-format="electronic">2782-3687</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">171</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>SOFT TISSUE SARCOMAS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>САРКОМЫ МЯГКИХ ТКАНЕЙ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Melatonic neuroectodermal tumor of infancy (melatonic progonoma): description of 3 patients</article-title><trans-title-group xml:lang="ru"><trans-title>Меланотическая нейроэктодермальная опухоль детей раннего возраста (меланотическая прогонома): описание трех случаев</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bliwyukov</surname><given-names>O. P.</given-names></name><name xml:lang="ru"><surname>Близнюков</surname><given-names>О. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>blisnukov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Center for Rhoentgenoradiology</institution></aff><aff><institution xml:lang="ru">ФГУ Российский научный центр рентгенорадиологии Росмедтехнологий</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2010-06-11" publication-format="electronic"><day>11</day><month>06</month><year>2010</year></pub-date><volume>2</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>44</fpage><lpage>48</lpage><history><date date-type="received" iso-8601-date="2022-01-11"><day>11</day><month>01</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2010, Bliwyukov O.P.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2010, Близнюков О.П.</copyright-statement><copyright-year>2010</copyright-year><copyright-holder xml:lang="en">Bliwyukov O.P.</copyright-holder><copyright-holder xml:lang="ru">Близнюков О.П.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://sarbon.abvpress.ru/jour/article/view/171">https://sarbon.abvpress.ru/jour/article/view/171</self-uri><abstract xml:lang="en"><p>A 4 and 8 month old boys and 1,5 year boy presented with a 6 week history of a skull mass of the anterior fontanelle. The mass was excised, and the histopathologic features were diagnostic for melanotic neuroectodermal tumor of infancy. The tumors consisted of a biphasic cell population in a fibrous stroma. The small, darkly staining cells comprising the first population stained positively for NSE, chromogranin and synaptophysin, showing them to be neuroblasts, and the large epithelioid cells comprising the second cell population stained positively with the antibodies CK7, HMB 45, Melan A and TTF 1, showing them to be melanocytes. Ultrastructural examination confirmed the biphasic nature of the tumor cells, with secretory granules and neurofilaments in the neuroblastic population, and melanosomes in the epithelioid population. It is the identification of the epithelioid cells in the smears which differentiates this tumor from other round cell tumors of infancy and helps in the correct diagnosis. These results add to the evidence supporting the neural crest origin of melanotic neuroectodermal tumor of infancy and confirm its formation from two distinct cell lines.</p></abstract><trans-abstract xml:lang="ru"><p>Меланотическая нейроэктодермальная опухоль (меланотическая прогонома) - редкая эмбриональная нейроэктодермальная опухоль, поражающая верхнюю челюсть и ткани височной ямки у детей в возрасте до двух лет. Опухоль обладает медленным инфильтративным ростом и в половине случаев рецидивирует после удаления в пределах здоровых тканей. Морфологический диагноз меланотической нейроэктодермальной опухоли труден, что связано со сложной структурой опухоли и редкими наблюдениями. Морфологический диагноз требует привлечения специальных методов исследования - иммуноморфологии и молекулярной биологии. Дифференциальный диагноз меланотической нейроэктодермальной опухоли проводят с нейробластомой, меланомой, альвеолярной рабдомиосаркомой и эстезионейробластомой. В работе приведено описании трех собственных наблюдений меланотической нейроэктодермальной опухоли.</p></trans-abstract><kwd-group xml:lang="en"><kwd>melanotic neuroectodermal tumor of infancy</kwd><kwd>melanotic progonoma</kwd><kwd>histopathology</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>меланотическая нейроэктодермальная опухоль</kwd><kwd>меланотическая прогонома</kwd><kwd>морфологическая диагностика</kwd><kwd>гистогенез</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Касумова С.Ю., Комаров В.И., Алииченко Л.А. Вопросы нейрохирургии. 1978, № 2, с. 46-49.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Стародумов В.В. Стоматология. 1985, № 3, с. 85-86.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Шендерева Т.С., Салита Н.В. Арх. патологии. 1989, № 2, с. 70-72.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Borello E.D., Gorlin R.J. Melanotic neuroectodermal tumor of infancy - a neoplasm of neural crest origin. Cancer. 1966, v. 19, p. 196-206.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Kapadia S.B., Frisman D.M., Hitchocock C.L. Melanotic neuroectodermal tumor of infancy. Clinicopathological, immunohistochemical and flow cytometric study. Am. J. Surg. Pathol. 1993, v. 17, p. 566-573.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Khoddami M., Squire J., Zielenska M. Melanotic neuroectodermal tumor of infancy. Pediatr. Dev. Pathol. 1998, v. 4, p. 295-299.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Krompecher E. Zur histogenese und morphologie der adamantinome und sonstiger kiefergeschwulste. Beitr. Pathol. Anat. 1918, v. 4, p. 165-197.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Pettinato G., Manivel C., d'Amore E.C. Melanotic neuroectodermal tumor of infancy. Am. J. Surg. Pathol. 1991, v. 15, p. 233-245.</mixed-citation></ref></ref-list></back></article>
