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            <front>

                <journal-meta>
                                                                <journal-id>genel tıp derg</journal-id>
            <journal-title-group>
                                                                                    <journal-title>Genel Tıp Dergisi</journal-title>
            </journal-title-group>
                                        <issn pub-type="epub">2602-3741</issn>
                                                                                            <publisher>
                    <publisher-name>Selcuk University</publisher-name>
                </publisher>
                    </journal-meta>
                <article-meta>
                                        <article-id/>
                                                                                                                                                                                            <title-group>
                                                                                                                                                            <article-title>Dirençli granülomatöz polianjiitis olgusu</article-title>
                                                                                                    </title-group>
            
                                                    <contrib-group content-type="authors">
                                                                        <contrib contrib-type="author">
                                                                <name>
                                    <surname>Limon</surname>
                                    <given-names>Muhammet</given-names>
                                </name>
                                                                    <aff>Selçuk Üniversitesi, Tıp Fakültesi, İç Hastalıkları Anabilim Dalı, Konya</aff>
                                                            </contrib>
                                                    <contrib contrib-type="author">
                                                                <name>
                                    <surname>Gülcemal</surname>
                                    <given-names>Semral</given-names>
                                </name>
                                                                    <aff>Selçuk Üniversitesi, Tıp Fakültesi, İç Hastalıkları Anabilim Dalı, Konya</aff>
                                                            </contrib>
                                                    <contrib contrib-type="author">
                                                                <name>
                                    <surname>Kanat</surname>
                                    <given-names>Fikret</given-names>
                                </name>
                                                                    <aff>Selçuk Üniversitesi, Tıp Fakültesi, Göğüs Hastalıkları Anabilim Dalı, Konya</aff>
                                                            </contrib>
                                                    <contrib contrib-type="author">
                                                                <name>
                                    <surname>Yılmaz</surname>
                                    <given-names>Sema</given-names>
                                </name>
                                                                    <aff>Selçuk Üniversitesi, Tıp Fakültesi, İç Hastalıkları Anabilim Dalı, Konya</aff>
                                                            </contrib>
                                                                                </contrib-group>
                        
                                        <pub-date pub-type="pub" iso-8601-date="20190301">
                    <day>03</day>
                    <month>01</month>
                    <year>2019</year>
                </pub-date>
                                        <volume>29</volume>
                                        <issue>2</issue>
                                        <fpage>95</fpage>
                                        <lpage>98</lpage>
                        
                        <history>
                                            </history>
                                        <permissions>
                    <copyright-statement>Copyright © 1990, Genel Tıp Dergisi</copyright-statement>
                    <copyright-year>1990</copyright-year>
                    <copyright-holder>Genel Tıp Dergisi</copyright-holder>
                </permissions>
            
                                                                                                <trans-abstract xml:lang="en">
                            <p>Vasculitis is a heterogeneous group of diseases characterized by inflammatory destruction of blood vessels. Vasculitis may result different clinical syndromes according to the characteristics of vasculitis. Vasculitides are separated as primers and secondary in the frequently used classification system, primer vasculitis is separated as small, mediıum and large vessel vasculitis according to its vascular involvement. Granulomatosis polyangitiis  GPA  is a small vessel vascülitis associated with ANCA. GPA may be seen with limited and systemic involvement. We presented this case to share treatment and side effects in cases of limited and systemic GPA</p></trans-abstract>
                                                                                                                                    <abstract><p>Vaskülitler, kan damarlarının inflamatuvardestrüksiyonu ile karakterize heterojen bir grup hastalıktır. Vaskülitler tutulan damar özelliğine göre klinik bulgu verebilir. Primer vaskülitler damar tutulum özelliklerine göre büyük, orta ve küçük damar vasküliti olarak ayrılır. Granülomatöz polianjiitis GPA  ANCA ilişkili küçük damar vaskülitidir. GPA sınırlı ve sistemik tutulumla seyredebilir. Bu olgu, akciğer tutulumu olan sistemik ve sınırlı GPA olgularında tedavive yan etkileri paylaşmak için sunulmuştur</p></abstract>
                                                            
            
                                                                                        <kwd-group>
                                                    <kwd>Vaskülit</kwd>
                                                    <kwd>   hemoptizi</kwd>
                                                    <kwd>   granülomatöz polianjiitis</kwd>
                                            </kwd-group>
                            
                                                <kwd-group xml:lang="en">
                                                    <kwd>Vasculitis</kwd>
                                                    <kwd>   hemoptysis</kwd>
                                                    <kwd>   granulomatosis polyangitiis</kwd>
                                            </kwd-group>
                                                                                                                                        </article-meta>
    </front>
    <back>
                            <ref-list>
                                    <ref id="ref1">
                        <label>1</label>
                        <mixed-citation publication-type="journal">Jenette JC, Folk RJ, Bacon K, et al. 2012 revised Interna- tional ChapelHillConsensus Conference Nomenclature of vasculitides. Arthritis Rheum 2013; 65: 1-11.</mixed-citation>
                    </ref>
                                    <ref id="ref2">
                        <label>2</label>
                        <mixed-citation publication-type="journal">Kallenberg CG. Antineutrophil cytoplasmic autoanti- body-associated small-vessel vasculitis. Curr Opin Rheu- matol 2007; 19.</mixed-citation>
                    </ref>
                                    <ref id="ref3">
                        <label>3</label>
                        <mixed-citation publication-type="journal">Eriksson P, Jacobsson L, Lindell A, Nilsson JA, Skogh T. Improvedoutcome in Wegener’sgranulomatosisandmic- roscopicpolyangiitis? A retrospectiveanalysis of 95 cases in twocohorts. J InternMed 2009; 265:496-506.</mixed-citation>
                    </ref>
                                    <ref id="ref4">
                        <label>4</label>
                        <mixed-citation publication-type="journal">Bosch X, Guilabert A, Font J. Antineutrophil cytoplasmic antibodies. Lancet 2006; 368: 404-18.</mixed-citation>
                    </ref>
                                    <ref id="ref5">
                        <label>5</label>
                        <mixed-citation publication-type="journal">Girard T, Mahr A, Noel LH, et al. Are antineutrophil cytoplasmic antibodies a marker predictive of relapse in Wegener’s granulomatosis? A prospectivestudy. Rheumato- logy (Oxford) 2001;40:147–51.</mixed-citation>
                    </ref>
                                    <ref id="ref6">
                        <label>6</label>
                        <mixed-citation publication-type="journal">Stegeman CA. Anti-neutrophil cytoplasmic antibody (ANCA) levels directed against proteinase-3 and mye- loperoxidase are helpful in predicting disease relapse in ANCA-associated small-vessel vasculitis. Nephrol Dial Transplant 2002; 17: 2077–80.</mixed-citation>
                    </ref>
                                    <ref id="ref7">
                        <label>7</label>
                        <mixed-citation publication-type="journal">Jayne D. Treatment of ANCA-associated systemic small vessel vasculitis. APMIS Suppl 2009; 127::3-9.</mixed-citation>
                    </ref>
                                    <ref id="ref8">
                        <label>8</label>
                        <mixed-citation publication-type="journal">Puécha X, Pagnoux C, Perrodeau É, et al. Long-term outco- mes among participants in the WEGENT trial of remissi- on-maintenance therapy for granulomatosis with polyangiitis (Wegener’s) or microscopic polyangiitis. Arth- ritis Rheumatol 2016;68:690–701.</mixed-citation>
                    </ref>
                                    <ref id="ref9">
                        <label>9</label>
                        <mixed-citation publication-type="journal">Carruthers D, Sherlock J. Evidence-based management of ANCA vasculitis. Best Pract Res Clin Rheumatol 2009; 23:367-78.</mixed-citation>
                    </ref>
                                    <ref id="ref10">
                        <label>10</label>
                        <mixed-citation publication-type="journal">Jayne D. Review article: Progress of treatment in ANCA-as- sociated vasculitis. Nephrology 2009;14:42-8.</mixed-citation>
                    </ref>
                                    <ref id="ref11">
                        <label>11</label>
                        <mixed-citation publication-type="journal">Pallan L, Savage CO, Harper L. ANCA-associated vasculitis: from bench research to novel treatments. Nat Rev Nephrol 2009;5:278-86.</mixed-citation>
                    </ref>
                                    <ref id="ref12">
                        <label>12</label>
                        <mixed-citation publication-type="journal">Specks U. Diffuse alveolar hemorrhage syndromes. Curr Opin Rheumatol 2001;13:12–7.</mixed-citation>
                    </ref>
                                    <ref id="ref13">
                        <label>13</label>
                        <mixed-citation publication-type="journal">Kobayashi S, Inokuma S. Intrapulmonary hemorrhage in collagen-vascular diseases includes a spectrum of under lying conditions. Intern Med 2009;48:891-7.</mixed-citation>
                    </ref>
                                    <ref id="ref14">
                        <label>14</label>
                        <mixed-citation publication-type="journal">Stone JH, Merkel PA, Spiera R, et al. RAVE-ITN research group, Rituximab versus cyclophosphamide for ANCA-as- sociated vasculitis. N Engl J Med2010:15;363:221.</mixed-citation>
                    </ref>
                                    <ref id="ref15">
                        <label>15</label>
                        <mixed-citation publication-type="journal">Puéchal X.Targeted immunotherapy strategies in AN- CA-associated vasculitis. Joint Bone Spine 2019;86:321-6.</mixed-citation>
                    </ref>
                                    <ref id="ref16">
                        <label>16</label>
                        <mixed-citation publication-type="journal">Smith R, Jones R, Specks U, et al. Rituximab as re-induction therapy in relapsing ANCA-associated vasculitis [abstract]. Arthritis Rheumatol 2017;69:18.</mixed-citation>
                    </ref>
                                    <ref id="ref17">
                        <label>17</label>
                        <mixed-citation publication-type="journal">Wegener’s Granulomatosis Etanercept Trial (WGET) Rese- arch Group. Etanercept plus standard therapy for Wegener’s granulomatosis. NEngl J Med 2005,352:351.</mixed-citation>
                    </ref>
                            </ref-list>
                    </back>
    </article>
