<?xml version="1.0" encoding="ISO-8859-1"?><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">
<front>
<journal-meta>
<journal-id>0873-2159</journal-id>
<journal-title><![CDATA[Revista Portuguesa de Pneumologia]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Port Pneumol]]></abbrev-journal-title>
<issn>0873-2159</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Pneumologia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0873-21592009000200011</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Exacerbação aguda da fibrose pulmonar idiopática]]></article-title>
<article-title xml:lang="en"><![CDATA[Acute exacerbation of idiopathic pulmonary fibrosis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Melo]]></surname>
<given-names><![CDATA[Natália]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Damas]]></surname>
<given-names><![CDATA[Carla]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Moura]]></surname>
<given-names><![CDATA[Conceição Souto]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Morais]]></surname>
<given-names><![CDATA[António]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Hospital de S. João Serviço de Pneumologia ]]></institution>
<addr-line><![CDATA[Porto ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2009</year>
</pub-date>
<volume>15</volume>
<numero>2</numero>
<fpage>305</fpage>
<lpage>312</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0873-21592009000200011&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0873-21592009000200011&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0873-21592009000200011&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Alguns doentes com fibrose pulmonar idiopática (FPI) apresentam durante a sua evolução fases deagravamento clínico sem causa conhecida, designadas como “exacerbação aguda” ou “fase acelerada” da doença (EA). Caracterizam -se pelo agravamento marcado da dispneia, hipoxemia e pelo aparecimento de novas opacidades pulmonares ou pelo agravamento das já existentes no estudo imagiológico. Os achados histológicos típicos são o dano alveolar difuso (DAD) sobreposto a alterações de pneumonia intersticial usual (UIP). Esta entidade clínica associa -se a uma mortalidade elevada, não havendo até ao momento nenhuma terapêutica de comprovada eficácia. Os autores descrevem os casos clínicos de cinco doentes que apresentaram alterações clínicas, funcionais e radiológicas sugestivas de EA-FPI, assim como o tratamento efectuado e a evolução observada, enquadrando-os na discussão das características normalmente apresentadas por esta entidade.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Some patients with Idiopathic Pulmonary Fibrosis (IPF) have disease accelerated deterioration without identifiable cause referred as “acute exacerbation” or “accelerated stage”. It is characterized by severe worsening of dyspnea, hypoxemia and new or progressive opacities on imaging studies. The typical histological findings are diffuse alveolar damage in addition to the features of usual interstitial pneumonia pattern. Mortality in this clinical entity is very high and no efficacious therapeutic have been described. The authors describe the clinical, functional and radiological features, treatment and evolution of five patients with IPF acute exacerbation. A discussion will be carry out concerning the IPF acute exacerbation usual features comparing with the alterations noticed in those patients.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Fibrose pulmonar idiopática]]></kwd>
<kwd lng="pt"><![CDATA[exacerbação aguda]]></kwd>
<kwd lng="en"><![CDATA[Idiopathic pulmonary fibrosis]]></kwd>
<kwd lng="en"><![CDATA[acute exacerbation]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p><b>Exacerbação aguda da fibrose pulmonar idiopática</b></p>      <p><b>&nbsp;</b></p>      <p><b>Natália Melo <a href="#1">1</a><a name="top1"></a></b></p>      <p><b>Carla Damas <a href="#2">2</a><a name="top2"></a></b></p>      <p><b>Conceição Souto Moura <a href="#3">3</a><a name="top3"></a></b></p>      <p><b>António Morais <a href="#2">2</a></b></p>     <p>&nbsp;</p>     <p>&nbsp;</p>      <p><b>Resumo</b></p>      <p>Alguns doentes com fibrose pulmonar idiopática (FPI) apresentam durante a sua evolução fases deagravamento clínico sem causa conhecida, designadas como “exacerbação aguda” ou “fase acelerada” da doença (EA). Caracterizam -se pelo agravamento marcado da dispneia, hipoxemia e pelo aparecimento de novas opacidades pulmonares ou pelo agravamento das já existentes no estudo imagiológico. Os achados histológicos típicos são o dano alveolar difuso (DAD) sobreposto a alterações de pneumonia intersticial usual (UIP). Esta entidade clínica associa -se a uma mortalidade elevada, não havendo até ao momento nenhuma terapêutica de comprovada eficácia.</p>      ]]></body>
<body><![CDATA[<p>Os autores descrevem os casos clínicos de cinco doentes que apresentaram alterações    clínicas, funcionais e radiológicas sugestivas de EA-FPI, assim como o tratamento    efectuado e a evolução observada, enquadrando-os na discussão das características    normalmente apresentadas por esta entidade.</p>     <p><b>Palavras -chave: </b>Fibrose pulmonar idiopática, exacerbação aguda.</p>      <p><b>&nbsp;</b></p>     <p>&nbsp;</p>     <p><b>Acute exacerbation of idiopathic pulmonary fibrosis</b></p>      <p><b>Abstract</b></p>      <p>Some patients with Idiopathic Pulmonary Fibrosis (IPF) have disease accelerated deterioration without identifiable cause referred as “acute exacerbation” or “accelerated stage”. It is characterized by severe worsening of dyspnea, hypoxemia and new or progressive opacities on imaging studies. The typical histological findings are diffuse alveolar damage in addition to the features of usual interstitial pneumonia pattern. Mortality in this clinical entity is very high and no efficacious therapeutic have been described.</p>      <p>The authors describe the clinical, functional and radiological features, treatment    and evolution of five patients with IPF acute exacerbation. A discussion will    be carry out concerning the IPF acute exacerbation usual features comparing    with the alterations noticed in those patients.</p>     <p><b>Key words: </b>Idiopathic pulmonary fibrosis, acute exacerbation.</p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>      <p>Texto completo dispon&iacute;vel apenas em PDF.</p>     <p>Full text only available in PDF format.</p>     <p>&nbsp;</p>     <p>&nbsp;</p>      <p><b>Bibliografia</b></p>      <!-- ref --><p>1. Kim DS, Collard HR, King TE Jr. Classification and natural history of idiopathic    interstitial pneumonias. The proceedings of the American Thoracic Society 2006;    3:285 -292.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000029&pid=S0873-2159200900020001100001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>2. Smith C, Feldman C, Levy H, <i>et al. </i>Cryptogenic fibrosing alveolitis: a study of an indigenous African population. Respiration (Herrlisheim) 1990; 57:364-371.</p>      <p>3. Katzenstein AL, Myers JL. Idiopathic pulmonary fibrosis. Clinical relevance    of pathologic classification. Am J Respir Crit Care Med 1998; 157:1301 -1315</p>      <p>4. American Thoracic Society / European Respiratory Society. Idiopathic pulmonary    fibrosis: diagnosis and treatment. International Consensus Statement. Am J Respir    Crit Care Med 2000; 161:646 -664.</p>      ]]></body>
<body><![CDATA[<p>5. Panos RJ, Mortenson R, Niccoli SA, <i>et al. </i>Clinical deterioration in patients with idiopathic pulmonary fibrosis: causes and assessment. Am J Med 1990; 88:396 -404.</p>      <p>6. Kondoh Y, Taniguchi H, Kawabata Y, <i>et al. </i>Acute exacerbation in idiopathic pulmonary fibrosis: analysis of clinical and pathologic findings in three cases. Chest 1993; 103: 1808 -1812.</p>      <p>7. Akira M, Hamada H, Sakatani M, <i>et al. </i>CT findings during phase of    accelerated deterioration in patients with idiopathic pulmonary fibrosis. Am    J Roentgenol 1997; 168:79 -83.</p>      <p>8. Ambrosini V, Cancellieri A, Chilosi M, <i>et al. </i>Acute exacerbation    of idiopathic pulmonary fibrosis: report of a series. Eur Respir J 2003; 22:821    -826.</p>      <p>9. Martinez FJ, Safrin S, Weycker D, <i>et al. </i>The clinical course of patients with idiopathic pulmonary fibrosis. Ann Intern Med 2005; 142:963 -967.</p>      <p>10. Azuma A, Nukwa T, Tsuboi E, <i>et al. </i>Double –blind placebo -controlled trial of pirfenidone in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2005; 171:1040 -1047.</p>      <p>11. Kim DS, Park JH, Park BK, <i>et al. </i>Acute exacerbation of idiopathic pulmonary fibrosis: frequency and clinical features. Eur Resp J 2006; 27:143 -150.</p>      <p>12. Hiwatari N, Shimura S, Takishima T, <i>et al. </i>Bronchoalveolar lavage as a possible cause of acute exacerbation in idiopathic pulmonary fibrosis patients. Tohoku J Exp Med 1994; 174:379 -386.</p>      <p>13. Kondoh Y, Taniguchi H, Kitaichi M, <i>et al. </i>Acute exacerbation of idiopathic pulmonary fibrosis following surgical lung biopsy. Respir Med 2006; 100:1753 -1759.</p>      <p>14. Yüksel M, Özyurtkan MO, Bostanci K, <i>et al. </i>Acute exacerbation of interstitial fibrosis after pulmonary resection. Ann Thorac Surg 2006; 82:336 -338.</p>      ]]></body>
<body><![CDATA[<p>15. Parambil JG, Myers JL, Ryu JH. Histopathologic features and outcome of patients with acute exacerbation of idiopathic pulmonary fibrosis undergoing surgical lung biopsy. Chest 2005; 128:3310 -3315.</p>      <p>16. Dallari R, Foglia M, Paci M, Cavazza A. Acute exacerbation of idiopathic    pulmonary fibrosis. Eur Respir J 2004; 23:792.</p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><a name="1"></a><a href="#top1">1</a> Interna Complementar de Pneumologia</p>     <p><a name="2"></a><a href="#top2">2</a> Assistente Hospitalar de Pneumologia</p>     <p>Serviço de Pneumologia do Hospital S. João – Director de Serviço: Prof. Dr.    Venceslau Hespanhol</p>     <p><a name="3"></a><a href="#top3">3</a> Assistente Hospitalar Graduada de Anatomia    Patológica</p>     <p>Serviço de Anatomia Patológica do Hospital S. João – Directora de Serviço:    Prof. Dra. Fátima Carneiro</p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p><b>Correspond&ecirc;ncia/<i>Correspondence to</i>:</b></p>     <p>Nat&aacute;lia Melo </p>     <p>Servi&ccedil;o de Pneumologia, Hospital de S. Jo&atilde;o </p>     <p>Alameda Professor Hern&acirc;ni Monteiro </p>     <p>4202-451 Porto </p>     <p>Telefone: 919371855 </p>     <p>e -mail: <a href="mailto:nataliafmelo@hotmail.com">nataliafmelo@hotmail.com</a></p>     <p>&nbsp;</p>     <p>Recebido para publica&ccedil;&atilde;o/<i>received for publication</i>: 08.04.11</p>     <p> Aceite para publica&ccedil;&atilde;o/<i>accepted for publication</i>: 08.11.07</p>      ]]></body>
<body><![CDATA[ ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Kim]]></surname>
<given-names><![CDATA[DS]]></given-names>
</name>
<name>
<surname><![CDATA[Collard]]></surname>
<given-names><![CDATA[HR]]></given-names>
</name>
<name>
<surname><![CDATA[King TE]]></surname>
<given-names><![CDATA[Jr.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Classification and natural history of idiopathic interstitial pneumonias.]]></article-title>
<source><![CDATA[The proceedings of the American Thoracic Society]]></source>
<year>2006</year>
<volume>3</volume>
<page-range>285 -292</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
