<?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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Allergy</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Allergy</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский Аллергологический Журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1810-8830</issn><issn publication-format="electronic">2686-682X</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">634</article-id><article-id pub-id-type="doi">10.36691/RJA634</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">PRIMARY IMMUNODEFICIENCIES - NOT A RARE DISEASE, BUT A DIFFICULT DIAGNOSIS. COMMON VARIABLE IMMUNODEFICIENCY (ANALYSIS OF CLINICAL CASES)</article-title><trans-title-group xml:lang="ru"><trans-title>ПЕРВИЧНЫЕ ИММУНОДЕФИЦИТЫ - НЕ РЕДКАЯ БОЛЕЗНЬ, А ТРУДНЫЙ ДИАГНОЗ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Latysheva</surname><given-names>E A</given-names></name><name xml:lang="ru"><surname>Латышева</surname><given-names>Е А</given-names></name></name-alternatives><email>ealat@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Institute of Immunology</institution></aff><aff><institution xml:lang="ru">ФГБУ «ГНЦ Институт иммунологии» ФМБА России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2013-02-15" publication-format="electronic"><day>15</day><month>02</month><year>2013</year></pub-date><volume>10</volume><issue>1</issue><issue-title xml:lang="en">NO1 (2013)</issue-title><issue-title xml:lang="ru">№1 (2013)</issue-title><fpage>58</fpage><lpage>61</lpage><history><date date-type="received" iso-8601-date="2020-03-10"><day>10</day><month>03</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2013, Pharmarus Print Media</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2013, Фармарус Принт Медиа</copyright-statement><copyright-year>2013</copyright-year><copyright-holder xml:lang="en">Pharmarus Print Media</copyright-holder><copyright-holder xml:lang="ru">Фармарус Принт Медиа</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2015-12-15"/></permissions><self-uri xlink:href="https://rusalljournal.ru/raj/article/view/634">https://rusalljournal.ru/raj/article/view/634</self-uri><abstract xml:lang="en"><p>Primary immunodeficiencies (PID) occur more often than we used to think. Due to the low awareness of physicians about this disease, from the onset of symptoms to diagnosis patients are difficult path, often measured in years. In PID adults the most common is humoral immunity disorder. Given the wide range of clinical phenotypes of the disease, immunologist may be far from the GP during diagnosis. The article presents a case of a patient with common variable immune deficiency, that was masked under the brain tumor.</p></abstract><trans-abstract xml:lang="ru"><p>Первичные иммунодефициты (ПИД) встречаются чаще, чем мы привыкли думать. В связи с низкой осведомленностью врачей о данной патологии от момента появления симптомов до установления диагноза пациенты проходят непростой путь, зачастую измеряющийся годами. У взрослых наиболее часто встречаются ПИД с нарушением в гуморальном звене иммунитета. Учитывая большое разнообразие клинических фенотипов данного заболевания, иммунолог может оказаться далеко не первым специалистом на этапе установления диагноза. В статье представлен клинический случай больной с общей вариабельной иммунной недостаточностью, у которой ПИД протекал под маской опухоли головного мозга.</p></trans-abstract><kwd-group xml:lang="en"><kwd>primary immunodeficiency</kwd><kwd>common variable immune deficiency</kwd><kwd>brain tumor</kwd><kwd>immunoglobulins</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>первичный иммунодефицит</kwd><kwd>общая вариабельная иммунная недостаточность</kwd><kwd>опухоль головного мозга</kwd><kwd>иммуноглобулины</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Marodi L., Notarangelo L.D. Immunological and genetic bases of new primary immunodeficiencies.NAT REV IMMUNOL. 2007, v. 7, p. 851-861.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>U.S. Department of Health and Human Services. National Institutes of Health. PAR-08-206: Investigations on Primary Immunodeficiency Diseases, 2009.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Bousfiha A.A., Jeddane L., Ailal F., Benhsaien I., Mahlaoui N., Casanova J.L., Abel L. Primary Immunodeficiency Diseases Worldwide: More Common than Generally Thought. J. Clin. Immunol. 2012, v. 31 (http://www.ncbi.nlm.nih.gov/pubmed?term=3.%09Bousfiha%20AA%2C%20Jeddane%20 L%2C%20Ailal%20F%2C%20Benhsaien%20I%2C%20 Mahlaoui%20N%2C%20Casanova%20JL%2C%20Abel%20L.%20Primary%20Immunodeficiency%20Diseases%20 Worldwide%3A%20More%20Common%20than%20Ge-nerall).</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Francisco A. Bonilla, Leonard Bernstein, David A. Khan, Zuhair K. Ballas et al. Practice parameter for the diagnosis and management of primary immunodeficiency. Annals of Allergy, Asthma and Immunology. 2005, v. 94, p. 1-60.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Ведение больных с первичным иммунодефицитом в акушерстве. Методические рекомендации для врачей под редакцией академика РАН и РАМН Р.М. Хаитова, академика РАМН Г.Т. Сухих. «Фармарус Принт Медиа», М., 2012, 5 с.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Aghamohammadi А., Abolhassani Н., Moazzami К., Parvaneh N., Rezaei N. Correlation Between Common Variable Immunodeficiency Clinical Phenotypes and Parental Consanguinity in Children and Adults. J. Investig Allergol Clin. Immunol. 2010, v. 20, p. 372-379.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Simon H.U., Späth P.J. IVIG-mechanisms of action. Allergy. 2003, v. 58, p. 543-552.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Pourpak Z., Aghamohammadi A., Sedighipour L., Farhoudi A., Movahedi M., Gharagozlou M. et al. Effect of regular intravenous immunoglobulin therapy on prevention of pneumonia in patients with common variable immunodeficiency. J. Microbiol. Immunol. Infect. 2006, v. 39, p. 114-120.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Vorechovsky I., Scott D., Haeney M.R., Webster D.A. Chromosomal radiosensitivity in common variable immune deficiency. Mutat. Res. 1993, v. 290, p. 255-264.</mixed-citation></ref></ref-list></back></article>
