<?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">MD-Onco</journal-id><journal-title-group><journal-title xml:lang="en">MD-Onco</journal-title><trans-title-group xml:lang="ru"><trans-title>MD-Onco</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2782-3202</issn><issn publication-format="electronic">2782-6171</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">96</article-id><article-id pub-id-type="doi">10.17650/2782-3202-2024-4-1-52-57</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>RARE AND COMPLEX CLINICAL SITUATIONS: DIAGNOSIS AND SELECTION OF TREATMENT TACTICS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>РЕДКИЕ И СЛОЖНЫЕ КЛИНИЧЕСКИЕ СИТУАЦИИ: ДИАГНОСТИКА И ВЫБОР ТАКТИКИ ЛЕЧЕНИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Nasopharyngeal arteriovenous malformation. Rare clinical observation</article-title><trans-title-group xml:lang="ru"><trans-title>Артериовенозная мальформация носоглотки. Редкое клиническое наблюдение</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1345-041X</contrib-id><name-alternatives><name xml:lang="en"><surname>Iurichev</surname><given-names>I. N.</given-names></name><name xml:lang="ru"><surname>Юричев</surname><given-names>И. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>111 1st Uspenskoe Shosse, Lapino, Moscow region 143081</p></bio><bio xml:lang="ru"><p>143081 Московская обл., д. Лапино, 1-е Успенское шоссе, 111</p></bio><email>ilia-yurichev@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6850-6919</contrib-id><name-alternatives><name xml:lang="en"><surname>Vereshchak</surname><given-names>V. V.</given-names></name><name xml:lang="ru"><surname>Верещак</surname><given-names>В. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>111 1st Uspenskoe Shosse, Lapino, Moscow region 143081</p></bio><bio xml:lang="ru"><p>143081 Московская обл., д. Лапино, 1-е Успенское шоссе, 111</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0918-3857</contrib-id><name-alternatives><name xml:lang="en"><surname>Mudunov</surname><given-names>A. M.</given-names></name><name xml:lang="ru"><surname>Мудунов</surname><given-names>А. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>111 1st Uspenskoe Shosse, Lapino, Moscow region 143081</p></bio><bio xml:lang="ru"><p>143081 Московская обл., д. Лапино, 1-е Успенское шоссе, 111</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Clinical Hospital “Lapino” of the “Mother and Child” Group of companies</institution></aff><aff><institution xml:lang="ru">Клинический госпиталь «Лапино» группы компаний «Мать и дитя»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-03-25" publication-format="electronic"><day>25</day><month>03</month><year>2024</year></pub-date><volume>4</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>52</fpage><lpage>57</lpage><history><date date-type="received" iso-8601-date="2024-03-25"><day>25</day><month>03</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-03-25"><day>25</day><month>03</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, ABV-Press</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, АБВ-пресс</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">ABV-Press</copyright-holder><copyright-holder xml:lang="ru">АБВ-пресс</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://mdonco.abvpress.ru/jour/about/editorialPolicies</ali:license_ref></license></permissions><self-uri xlink:href="https://mdonco.abvpress.ru/jour/article/view/96">https://mdonco.abvpress.ru/jour/article/view/96</self-uri><abstract xml:lang="en"><p>Arteriovenous malformation (AVM) of the head and neck is a rare disease developing during embryo- and vasculogenesis due to RASA1 mutation which is inherited in accordance with autosomal dominant pattern and is associated with CMC1 locus on the long arm of the 5th chromosome 5q13.3. Statistically, AVMs are rarer than other congenital vascular abnormalities such as lymphatic or venous malformations. While AVMs are non-malignant neoplasms, among all vascular abnormalities they are the most aggressive, destructive and complex in their structure. In international literature, a small number of articles describing cases of this pathology exists (for example, I.T. Jackson et al. analyzed 16 cases of this pathology, M.T. Chen et al. reported on 14 cases, M.P. Kohaut et al. analyzed 81 cases of extracranial AVMs).In Russin literature, the number of articles describing clinical cases of AVM is in the single digits, and this topic remains quite relevant. The article presents a rare clinical observ</p></abstract><trans-abstract xml:lang="ru"><p>Артериовенозная мальформация (АВМ) области головы и шеи – редкое заболевание, возникающее в процессе эмбрио- и васкулогенеза ввиду мутации RASA1, которая наследуется по аутосомно-доминантному типу и связана с локусом CMC1 на длинном плече 5-й хромосомы 5q13.3. По статистике, АВМ встречаются реже, чем другие врожденные пороки развития сосудов, такие как лимфатические или венозные мальформации. Несмотря на то что АВМ – незлокачественные новообразования, они являются наиболее агрессивными, деструктивными и сложными в плане строения из всех сосудистых аномалий. В зарубежной литературе имеются немногочисленные работы с описанием случаев данной патологии (например, I.T. Jackson и соавт. проанализировали 16 случаев патологии, M.T. Chen и соавт. сообщили о 14 случаях, M.P. Kohaut и соавт. проанализировали 81 случай с экстракраниальными АВМ). В отечественной литературе работы с описанием клинических случаев АВМ единичны, поэтому тема остается достаточно актуальной.В статье представлено редкое клиническое наблюдение АВМ полости носоглотки и ротоглотки с формированием менингоэнцефалоцеле у пациентки 34 лет.</p></trans-abstract><kwd-group xml:lang="en"><kwd>arteriovenous malformation</kwd><kwd>vascular pathology</kwd><kwd>meningoencephalocele</kwd><kwd>rare clinical case</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>артериовенозная мальформация</kwd><kwd>патология сосудов</kwd><kwd>менингоэнцефалоцеле</kwd><kwd>редкий клинический случай</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Milliken J.B., Glowacki J. Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics. Plast Reconstr Surg 1982;69(3):412–22. DOI: 10.1097/00006534-198203000-00002</mixed-citation></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Goncharova Ya.A. Hemangiomas and vascular malformations. Modern theories and therapeutic tactics. Zdorovye rebenka = Childʼs Health 2013;6(49):148–52.</mixed-citation><mixed-citation xml:lang="ru">Гончарова Я.А. Гемангиомы и сосудистые мальформации. Современные теории и лечебная тактика. Здоровье ребенка 2013;6(49):148–52. .</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><mixed-citation>Chen M.T., Horng S.Y., Yeong E.K., Pan Q.D. Treatment of highflow vascular malformations in the head and neck with arterial ligation followed by sclerotherapy. Ann Plast Surg 1996;36(2):147–53. DOI: 10.1097/00000637-199602000-00007</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Jin Y., Lin X., Chen H. et al. Auricular arteriovenous malformations: potential success of superselective ethanol embolotherapy. J Vasc Interv Radiol 2009;20(6):736–43. DOI: 10.1016/j.jvir.2009.02.008</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Kohout M.P., Hansen M., Pribaz J., Mulliken J.B. Arteriovenous malformations of the head and neck: natural history and management. Plast Reconstr Surg 1998;102(3):643–54. DOI: 10.1097/00006534-199809030-00006</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Pekkola J., Lappalainen K., Vuola P. et al. Head and neck arterio-venous malformations: results of ethanol sclerotherapy. AJNR Am J Neuroradiol 2013;34(1):198–204. DOI: 10.3174/ajnr.A3180</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Vogelzang R.L., Atassi R., Vouche M. et al. Ethanol embolotherapy of vascular malformations: clinical outcomes at a single center. J Vasc Interv Radiol 2014;25(2):206–13; quiz 214. DOI: 10.1016/j.jvir.2013.10.055</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Griauzde J., Srinivasan A. Imaging of vascular lesions of the head and neck. Radiol Clin North Am 2015;53(1):197–213. DOI: 10.1016/j.rcl.2014.09.001</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Eivazi B., Werner J.A. Management of vascular malformations and hemangiomas of the head and neck – an update. Curr Opin Otolaryngol Head Neck Surg 2013;21(2):157–63. DOI: 10.1097/MOO.0b013e32835e15a9</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Burns J.C., Julian J., Alexander J. Arteriovenous malformation of the submandibular gland. J Oral Maxillofac Surg 1985;43(4):294–6. DOI: 10.1016/0278-2391(85)90292-7</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Schobinger R.A. [Diagnostic and therapeutic possibilities in peripheral angiodysplasias (In German)]. Helv Chir Acta 1971;38(3):213–20.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Jeong H.S., Baek C.H., Son Y.I. et al. Treatment for extracranial arteriovenous malformations of the head and neck. Acta Otolaryngol 2006;126(3):295–300. DOI: 10.1080/00016480500388950</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Jackson I.T., Carreño R., Potparic Z., Hussain K. Hemangiomas, vascular malformations, and lymphovenous malformations: classification and methods of treatment. Plast Reconstr Surg 1993;91(7):1216–30. DOI: 10.1097/00006534-199306000-00006</mixed-citation></ref></ref-list></back></article>
