<?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>S0873-21592008000100007</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Sarcoidose extratorácica]]></article-title>
<article-title xml:lang="en"><![CDATA[Extra-thoracic sarcoidosis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Costa]]></surname>
<given-names><![CDATA[Filipa]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arrobas]]></surname>
<given-names><![CDATA[Ana]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Centro Hospitalar de Coimbra Serviço de Pneumologia ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>02</month>
<year>2008</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>02</month>
<year>2008</year>
</pub-date>
<volume>14</volume>
<numero>1</numero>
<fpage>127</fpage>
<lpage>140</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0873-21592008000100007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0873-21592008000100007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0873-21592008000100007&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[A sarcoidose é uma doença granulomatosa multissistémica de etiologia desconhecida, caracterizada histologicamente pela presença de granulomas não caseosos nos órgãos envolvidos. Trata-se de uma doença que pode envolver praticamente qualquer órgão, manifestando-se de múltiplas formas e apresentando-se a várias especialidades clínicas. O envolvimento extratorácico isolado é raro (10%), surgindo mais frequentemente associado ao envolvimento pulmonar ou dos gânglios linfáticos mediastínicos. A nível extratorácico pode ocorrer, entre outros, envolvimento do fígado (50-80%), baço (40-80%), olho (20-50%), nódulos linfáticos periféricos (30%), pele (25%), sistema nervoso (10%), coração (5%), rim e aparelho músculo-esquelético, nem sempre cursando com sintomatologia. A presença de envolvimento extratorácico afecta muitas vezes o prognóstico e a atitude terapêutica da sarcoidose. Os autores fazem uma revisão das principais manifestações extratorácicas da sarcoidose, abordando as suas manifestações clínicas, diagnóstico, tratamento, seguimento e prognóstico.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Sarcoidosis is a multisystemic granulomatous disease of unknown aetiology, characterized by the presence of non-caseating epithelioid cell granulomas on tissue biopsy of affected organs. It may involve any organ, presenting in multiple forms to clinicians of different specialities. In its extra-thoracic form it may involve the liver (50-80%), spleen (40-80%), eye (20-50%), extrathoracic lymph nodes (30%), skin (25%), nervous system (10%), heart (5%), kidney, muscle and bone, sometimes without symptoms. The presence of extrathoracic disease may affect the prognosis and treatment options for sarcoidosis. The authors present a review of the major extra-thoracic manifestations of sarcoidosis regarding its clinical presentation, diagnosis, treatment, follow-up and prognosis.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Sarcoidose]]></kwd>
<kwd lng="pt"><![CDATA[extratorácica]]></kwd>
<kwd lng="en"><![CDATA[Sarcoidosis]]></kwd>
<kwd lng="en"><![CDATA[extra-thoracic]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p><b>Sarcoidose extratorácica</b></p>      <p><b>Extra-thoracic sarcoidosis</b></p>     <p>&nbsp;</p>          <p><b>Filipa Costa <a href="#1">1</a><a name="top1"></a></b></p>      <p><b>Ana Arrobas <a href="#2">2</a><a name="top2"></a></b></p>     <p>&nbsp;</p>          <p><b>Resumo</b></p>      <p>A sarcoidose é uma doença granulomatosa multissistémica de etiologia desconhecida, caracterizada histologicamente pela presença de granulomas não caseosos nos órgãos envolvidos. Trata-se de uma doença que pode envolver praticamente qualquer órgão, manifestando-se de múltiplas formas e apresentando-se a várias especialidades clínicas. O envolvimento extratorácico isolado é raro (10%), surgindo mais frequentemente associado ao envolvimento pulmonar ou dos gânglios linfáticos mediastínicos.</p>      <p>A nível extratorácico pode ocorrer, entre outros, envolvimento do fígado (50-80%), baço (40-80%), olho (20-50%), nódulos linfáticos periféricos (30%), pele (25%), sistema nervoso (10%), coração (5%), rim e aparelho músculo-esquelético, nem sempre cursando com sintomatologia. A presença de envolvimento extratorácico afecta muitas vezes o prognóstico e a atitude terapêutica da sarcoidose.</p>      <p>Os autores fazem uma revisão das principais manifestações extratorácicas da sarcoidose, abordando as suas manifestações clínicas, diagnóstico, tratamento, seguimento e prognóstico.</p>         ]]></body>
<body><![CDATA[<p><b>Palavras-chave: </b>Sarcoidose, extratorácica.</p>     <p>&nbsp;</p>     <p>&nbsp;</p>      <p><b>Abstract</b></p>      <p>Sarcoidosis is a multisystemic granulomatous disease of unknown aetiology, characterized by the presence of non-caseating epithelioid cell granulomas on tissue biopsy of affected organs. It may involve any organ, presenting in multiple forms to clinicians of different specialities.</p>      <p>In its extra-thoracic form it may involve the liver (50-80%), spleen (40-80%), eye (20-50%), extrathoracic lymph nodes (30%), skin (25%), nervous system (10%), heart (5%), kidney, muscle and bone, sometimes without symptoms. The presence of extrathoracic disease may affect the prognosis and treatment options for sarcoidosis.</p>      <p>The authors present a review of the major extra-thoracic manifestations of sarcoidosis regarding its clinical presentation, diagnosis, treatment, follow-up and prognosis.</p>                 <p><b>Key-words: </b>Sarcoidosis, extra-thoracic.</p>     <p>&nbsp;</p>       <p>Texto completo dispon&iacute;vel apenas em PDF.</p>        ]]></body>
<body><![CDATA[<p>Full text only available in PDF format.</p>     <p>&nbsp;</p>     <p>&nbsp;</p>             <p><b>Bibliografia</b></p>     <p>&nbsp;</p>      <!-- ref --><p>1. Costabel U. Sarcoidosis: clinical update. Eur Respir J 2001; 18(Suppl 32):56s-68s.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000028&pid=S0873-2159200800010000700001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>2. Costabel U, Hunninghake GW. ATS/ERS/WASOG statement on sarcoidosis. Eur Respir J 1999; 14:735-7.</p>      <p>3. Moller RD. Rare manifestations of sarcoidosis. Eur Respir Mon 2005; 32:233-50.</p>      <p>4. James DG, Sherlock S. Sacoidosis of the liver. Sarcoidosis 1994; 11:2-6.</p>      <p>5. Vatti R, Sharma OP. Course of asymptomatic liver involvement in sarcoidosis: role of therapy in selected cases. Sarcoidosis Vasc Diffuse Lung Dis 1997; 14:73-6.</p>      ]]></body>
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<body><![CDATA[<p>16. Warshauder DM, Dumbleton SA, Molina PL, <i>et al</i>. Abdominal CT findings in sarcoidosis: radiological and clinical correlation. Radiology 1994; 192:93-8.</p>      <p>17. Eklund A, Rizzato G. Skin manifestations in sarcoidosis. Eur Respir Mon 2005; 32:150-63.</p>      <p>18. Mana J, Marcoval J, Graells J, <i>et al</i>. Cutaneous involvement in sarcoidosis. Arch Dermatol 1997; 133:882-8.</p>      <p>19. Russo G, Millikan LE. Cutaneous sarcoidosis: diagnosis and treatment. Comp Ther 1994; 20:418-21.</p>      <p>20. Volden G. Successful treatment of chronic skin diseases with clobetasol propio nate and a hydrocolloid occlusive dressing. Acta Derm Venereol 1992; 72:69-71.</p>      <p>21. Newman LS, Rose CS, Maier LA. Sarcoidosis. N Engl J Med 1997; 336:1224-34.</p>      <p>22. Zic JA, Horowitz DH, Arzubiaga C, <i>et al</i>. Treatment of cutaneous sarcoidosis with chloroquine. Arch Dermatol 1991; 127:1034-40.</p>      <p>23. Jones E, Callen JF. Hydroxychloroquine is effective therapy for control of cutaneous sacoidal granulomas. J Acad Dermatol 1990; 23:487-9.</p>      <p>24. Webster GF, Razki LK, Sanchez M, <i>et al</i>. Weekly low-dose methotrexate therapy for cutaneous sarcoidosis. J Am Acad Dermatol 1991; 24:451-4.</p>      <p>25. Pollock JL. Sarcoidosis responding to allopurinol. Arch Dermatol 1980; 116:273-4.</p>      ]]></body>
<body><![CDATA[<p>26. Carlesimo M, Guistini S, Rossi A, <i>et al</i>. Treatment of cutaneous and pulmonary sarcoidosis with thalidomide. J Am Acad Dermatol 1995; 32:866-9.</p>      <p>27. Hoitsma E, Sharma OP. Neurosarcoidosis. Eur Respir Mon 2005; 32:164-87.</p>      <p>28. Sharma OP. Cardiac and neurologic dysfunction in sarcoidosis. Clin Chest    Med 1997; 18:813-25. </p>     <p>29. Stern BJ, Krumholz A, Johns C, <i>et al</i>. Sarcoidosis and its neurological    manifestations. Arch Neurol 1985; 42:909-17.</p>      <p>30. Agbogu BN, Stern BJ, Sewell C, <i>et al</i>. Therapeutic considerations in patients with refractory neurosarcoidosis. Arch Neurol 1995; 52:875-9.</p>      <p>31. Schulte W, Kirsten D, Drent M, Costabel U. Cardiac involvement in sarcoidosis. Eur Respir Mon 2005; 32:130-49.</p>      <p>32. Sekiguchi M, Yazaki Y, Isobe M, <i>et al</i>. Cardiac sarcoidosis: diagnostic, prognostic and thera peutic considerations. Cardiovasc Drugs Ther 1996; 10:495-510.</p>      <p>33. Baughman RP, Lower EE. Steroid sparing alternative treatments for sarcoidosis. Clin Chest Med 1997; 18:853-64.</p>      <p>34. Shammas RL, Movahed A. Sarcoidosis of the heart. Clin Cardiol 1993; 16:462-72.</p>      <p>35. Chin BB, Civelek AC, Mudun A. Resting T-201 scintigraphy in the evaluation of myocardial sarcoidosis. Clin Nucl Med 1997; 22:475-8.</p>      ]]></body>
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<body><![CDATA[<p>46. Kaye O, Palazzo E, Grossin M, <i>et al</i>. Low-dose methotrexate: an effective corticosteroid-sparing agent in musculoskeletal manifestations of sarcoidosis. Br J Rheumatol 1995; 34:642-4.</p>      <p>47. Judson MA, Baughman RP, Terstein AS, <i>et al</i>. Defining organ involvement in sarcoidosis: the ACCESS proposed instrument. Sarcoidosis Vasc Diffuse Lung Dis 1999; 16:75-86.</p>      <p>48. Kennedy D, Yamakido M. Haematologic manifestations of sarcoidosis. Semin Respir Med 1992; 13:455-8.</p>      <p>49. Browne PM, Sharma OP, Salkin D. Bone marrow sarcoidosis. JAMA 1978; 240:2654-5.</p>      <p>50. Bower JS, Belen JE, Weg JG, <i>et al</i>. Manifestations and treatment of laryngeal sarcoidosis. Am Rev Respir Dis 1980; 122:325-32.</p>      <p>51. Krespi YP, Kuriloff DB, Aner M. Sarcoidosis of the sinonasal tract: a new staging system. Otolaryngol Head Neck Surg 1995; 112:221-7.</p>      <p>52. Shah UK, White JA, Gooey JE, <i>et al</i>. Otolaryngologic manifestations of sarcoidosis: presentation and diagnosis. Laryngoscope 1997; 107:67-75.</p>         <p>53. Scheffield EA. Pathology of sarcoidosis. Clin Chest Med 1997; 18:741-54.</p>     <p>&nbsp;</p>     <p>&nbsp;</p>              ]]></body>
<body><![CDATA[<p><a name="1"></a><a href="#top1">1</a> Interna do Internato Complementar de    Pneumologia</p>     <p><a name="2"></a><a href="#top2">2</a> Assistente Hospitalar Graduada de Pneumologia</p>       <p>Serviço de Pneumologia,</p>       <p>Centro Hospitalar de Coimbra</p>       <p>(Director: Dr. Jorge Pires)</p>       <p>Quinta dos Vales</p>       <p>São Martinho do Bispo</p>        <p>3046-853 Coimbra</p>     <p>&nbsp;</p>     <p>Recebido para publicação/received for publication: 07.02.23</p>     ]]></body>
<body><![CDATA[<p>Aceite para publicação/accepted for publication: 07.07.20</p>       ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Costabel]]></surname>
<given-names><![CDATA[U.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Sarcoidosis: clinical update]]></article-title>
<source><![CDATA[Eur Respir J]]></source>
<year>2001</year>
<volume>18</volume>
<numero>32</numero>
<issue>32</issue>
<page-range>56s-68s</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
