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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">rsp</journal-id><journal-title-group><journal-title xml:lang="ru">Научно-практическая ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Rheumatology Science and Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1995-4484</issn><issn pub-type="epub">1995-4492</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14412/1995-4484-2016-598-600</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-2309</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>КЛИНИЧЕСКОЕ НАБЛЮДЕНИЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL OBSERVATIONS</subject></subj-group></article-categories><title-group><article-title>СИНДРОМ  КОГАНА. КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ УСПЕХ  ИММУНОСУПРЕССИВНОЙ  ТЕРАПИИ</article-title><trans-title-group xml:lang="en"><trans-title>COGAN'S SYNDROME: SUCCESS OF IMMUNOSUPPRESSIVE THERAPY</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>Морова</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Morova</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Наталия Александровна Морова.</p><p>1644043 Омск, ул. Ленина, 12</p></bio><bio xml:lang="en"><p>Nataliya Morova.</p><p>12, LeninSt., Omsk644043</p></bio><email xlink:type="simple">nataliya-morova@yandex.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>Кропотина</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kropotina</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>2644111 Омск, ул. Березовая, 3</p></bio><bio xml:lang="en"><p>3, BerezovayaSt., Omsk 644111</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>Арбузова</surname><given-names>Ю. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Arbuzova</surname><given-names>Yu. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>2644111 Омск, ул. Березовая, 3</p></bio><bio xml:lang="en"><p>3, BerezovayaSt., Omsk 644111</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Омский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Omsk State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Областная клиническая больница</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Regonal  Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>09</day><month>12</month><year>2016</year></pub-date><volume>54</volume><issue>5</issue><fpage>598</fpage><lpage>600</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Морова Н.А., Кропотина Т.В., Арбузова Ю.В., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Морова Н.А., Кропотина Т.В., Арбузова Ю.В.</copyright-holder><copyright-holder xml:lang="en">Morova N.A., Kropotina T.V., Arbuzova Y.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://rsp.mediar-press.net/rsp/article/view/2309">https://rsp.mediar-press.net/rsp/article/view/2309</self-uri><abstract><p>Синдром  Когана – редкое заболевание из группы системных васкулитов с вариабельным поражением сосудов. Представляет  собой сочетание  офтальмологических симптомов  и аудиовестибулярных расстройств (синдром  Меньера и сенсоневральная тугоухость). Часто наблюдаются  лихорадка, артралгии или артрит, встречаются неврологические нарушения, аортит с развитием  аневризмы аорты. Потеря  слуха часто бывает необратимой. Изменения со стороны органа зрения обычно протекают благоприятно.</p></abstract><trans-abstract xml:lang="en"><p>Cogan's syndrome is a rare disease from a group of systemic vasculitides with variable vascular involvement. It is a concurrence of ophthalmic  symptoms and audiovestibular disorders (Meniere's disease and sensorineural hearing loss). There is often fever, arthralgia or arthritis; neurological disorders and aortitis with the development of aortic aneurysms are encountered. Hearing loss is frequently irreversible. Changes in the organ of vision usually occur favorably.</p><p>The paper describes a case of Cogan's syndrome in a 33-year-old  patient. The disease is manifested by papilledema, conjunctivitis, acute sensorineural deafness with rapid loss of hearing, and microfocal changes in the brain, as detected by computed  tomography. Pulse therapy with glucocorticoids  and cyclophosphamide led to a rapid and obvious regression of all symptoms. The case is of interest due to the rare occurrence  of the disease and to the success of performed therapy. The description stresses the importance  of a rheumatologist's  consultation  and the need for the collective management of young patients with clinical presentations  of acute sensorineural hearing loss.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>системные  васкулиты</kwd><kwd>синдром Когана</kwd><kwd>острая сенсоневральная тугоухость</kwd><kwd>глюкокортикоиды</kwd><kwd>циклофосфан</kwd></kwd-group><kwd-group xml:lang="en"><kwd>systemic vasculitides</kwd><kwd>Cogan's syndrome</kwd><kwd>acute sensorineural hearing loss</kwd><kwd>glucocorticoids</kwd><kwd>cyclophosphamide</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">Morgan RF, Baumgartner CJ. Meniers disease complicated by recurrent interstitial keratitis: excellent results following cervical ganglionectomy. West J Surg. 1934;42:628-31.</mixed-citation><mixed-citation xml:lang="en">Morgan RF, Baumgartner CJ. 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