Silicose et syndrome de Gougerot-Sjögren primitif
Identifieur interne : 001039 ( Istex/Corpus ); précédent : 001038; suivant : 001040Silicose et syndrome de Gougerot-Sjögren primitif
Auteurs : F. Puisieux ; E. Hachulla ; M. Brouillard ; Py Hatron ; B. DevulderSource :
- La Revue de medecine interne [ 0248-8663 ] ; 1994.
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Abstract
Résumé: Les auteurs rapportent trois observations de syndrome de Gougerot-Sjögren primitif chez des mineurs de charbon atteints d'anthracosilicose. Tous les patients remplissaient les critères diagnostiques du syndrome de Gougerot-Sjögren primitif récemment établis par le groupe d'étude de la Communauté européenne. Ils avaient une xérostomie et une xérophtalmie sévères. Un patient avait une cryoglobulinémie et une polynévrite. Un autre avait un phénomène de Raynaud, des arthralgies, un purpura et une polynévrite. La capillaroscopie était normale dans les trois cas, des anticorps antinucléaires étaient détectés chez un seul patient (anticorps anti-SSA et anti-SSB). La prévalence de la sclérodermie systémique, de la polyarthrite rhumatoïde et probablement du lupus érythémateux disséminé est significativement plus élevée après exposition professionnelle prolongée à la silice. En revanche, aucun cas de syndrome de Gougerot-Sjögren primitif associé à une silicose pulmonaire n'a encore été rapporté. Les mécanismes physiopathologiques de ces associations sont mal connus.
Summary: We report three cases of primary Sjögren's syndrome in silicotic coal miners. All patients fulfilled the diagnostic criteria for Sjögren's syndrome recently established by the European Community study group. One patient had cryoglobulinemia and polynevritis. Another had Raynaud's phenomenom, arthralgia, purpura and polynevritis. Capillary microscopy was normal in all the three patients. Antinuclear antibodies were detected only in one patient, who had also anti-SSa and anti-SSb antibodies. The prevalence of systemic sclerosis, rheumatoid arthritis and probably systemic lupus erythematosus is significantly higher after longstanding occupational exposure to silica. On the contrary, any case of Sjögren's syndrome was till now described in the course of pulmonary silicosis. The physiopathological mechanisms of these associations are misunderstood.
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DOI: 10.1016/S0248-8663(05)82502-0
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Tous les patients remplissaient les critères diagnostiques du syndrome de Gougerot-Sjögren primitif récemment établis par le groupe d'étude de la Communauté européenne. Ils avaient une xérostomie et une xérophtalmie sévères. Un patient avait une cryoglobulinémie et une polynévrite. Un autre avait un phénomène de Raynaud, des arthralgies, un purpura et une polynévrite. La capillaroscopie était normale dans les trois cas, des anticorps antinucléaires étaient détectés chez un seul patient (anticorps anti-SSA et anti-SSB). La prévalence de la sclérodermie systémique, de la polyarthrite rhumatoïde et probablement du lupus érythémateux disséminé est significativement plus élevée après exposition professionnelle prolongée à la silice. En revanche, aucun cas de syndrome de Gougerot-Sjögren primitif associé à une silicose pulmonaire n'a encore été rapporté. Les mécanismes physiopathologiques de ces associations sont mal connus.</div><div type="abstract" xml:lang="en">Summary: We report three cases of primary Sjögren's syndrome in silicotic coal miners. All patients fulfilled the diagnostic criteria for Sjögren's syndrome recently established by the European Community study group. One patient had cryoglobulinemia and polynevritis. Another had Raynaud's phenomenom, arthralgia, purpura and polynevritis. Capillary microscopy was normal in all the three patients. Antinuclear antibodies were detected only in one patient, who had also anti-SSa and anti-SSb antibodies. The prevalence of systemic sclerosis, rheumatoid arthritis and probably systemic lupus erythematosus is significantly higher after longstanding occupational exposure to silica. On the contrary, any case of Sjögren's syndrome was till now described in the course of pulmonary silicosis. The physiopathological mechanisms of these associations are misunderstood.</div></front></TEI><istex><corpusName>elsevier</corpusName><author><json:item><name>F Puisieux</name><affiliations><json:string>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</json:string></affiliations></json:item><json:item><name>E Hachulla</name><affiliations><json:string>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</json:string></affiliations></json:item><json:item><name>M Brouillard</name><affiliations><json:string>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</json:string></affiliations></json:item><json:item><name>PY Hatron</name><affiliations><json:string>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</json:string></affiliations></json:item><json:item><name>B Devulder</name><affiliations><json:string>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>fre</json:string></lang><value>silicose</value></json:item><json:item><lang><json:string>fre</json:string></lang><value>pneumoconiose</value></json:item><json:item><lang><json:string>fre</json:string></lang><value>Gougerot-Sjögren</value></json:item><json:item><lang><json:string>fre</json:string></lang><value>connectivite</value></json:item><json:item><lang><json:string>fre</json:string></lang><value>silicosis</value></json:item><json:item><lang><json:string>fre</json:string></lang><value>pneumoconiosis</value></json:item><json:item><lang><json:string>fre</json:string></lang><value>Sjögren's syndrome</value></json:item><json:item><lang><json:string>fre</json:string></lang><value>connective tissue diseases</value></json:item></subject><articleId><json:string>05825020</json:string></articleId><arkIstex>ark:/67375/6H6-PCKZ3PZG-W</arkIstex><language><json:string>fre</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Résumé: Les auteurs rapportent trois observations de syndrome de Gougerot-Sjögren primitif chez des mineurs de charbon atteints d'anthracosilicose. Tous les patients remplissaient les critères diagnostiques du syndrome de Gougerot-Sjögren primitif récemment établis par le groupe d'étude de la Communauté européenne. Ils avaient une xérostomie et une xérophtalmie sévères. Un patient avait une cryoglobulinémie et une polynévrite. Un autre avait un phénomène de Raynaud, des arthralgies, un purpura et une polynévrite. La capillaroscopie était normale dans les trois cas, des anticorps antinucléaires étaient détectés chez un seul patient (anticorps anti-SSA et anti-SSB). La prévalence de la sclérodermie systémique, de la polyarthrite rhumatoïde et probablement du lupus érythémateux disséminé est significativement plus élevée après exposition professionnelle prolongée à la silice. En revanche, aucun cas de syndrome de Gougerot-Sjögren primitif associé à une silicose pulmonaire n'a encore été rapporté. 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Tous les patients remplissaient les critères diagnostiques du syndrome de Gougerot-Sjögren primitif récemment établis par le groupe d'étude de la Communauté européenne. Ils avaient une xérostomie et une xérophtalmie sévères. Un patient avait une cryoglobulinémie et une polynévrite. Un autre avait un phénomène de Raynaud, des arthralgies, un purpura et une polynévrite. La capillaroscopie était normale dans les trois cas, des anticorps antinucléaires étaient détectés chez un seul patient (anticorps anti-SSA et anti-SSB). La prévalence de la sclérodermie systémique, de la polyarthrite rhumatoïde et probablement du lupus érythémateux disséminé est significativement plus élevée après exposition professionnelle prolongée à la silice. En revanche, aucun cas de syndrome de Gougerot-Sjögren primitif associé à une silicose pulmonaire n'a encore été rapporté. Les mécanismes physiopathologiques de ces associations sont mal connus.</p></abstract><abstract xml:lang="en"><p>Summary: We report three cases of primary Sjögren's syndrome in silicotic coal miners. All patients fulfilled the diagnostic criteria for Sjögren's syndrome recently established by the European Community study group. One patient had cryoglobulinemia and polynevritis. Another had Raynaud's phenomenom, arthralgia, purpura and polynevritis. Capillary microscopy was normal in all the three patients. Antinuclear antibodies were detected only in one patient, who had also anti-SSa and anti-SSb antibodies. The prevalence of systemic sclerosis, rheumatoid arthritis and probably systemic lupus erythematosus is significantly higher after longstanding occupational exposure to silica. On the contrary, any case of Sjögren's syndrome was till now described in the course of pulmonary silicosis. The physiopathological mechanisms of these associations are misunderstood.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>silicose</term></item><item><term>pneumoconiose</term></item><item><term>Gougerot-Sjögren</term></item><item><term>connectivite</term></item></list></keywords></textClass><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>silicosis</term></item><item><term>pneumoconiosis</term></item><item><term>Sjögren's syndrome</term></item><item><term>connective tissue diseases</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1994">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-PCKZ3PZG-W/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier doc found" wicri:toSee="Elsevier, no converted or simple article"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 5.0.1//EN//XML" URI="art501.dtd" name="istex:docType"></istex:docType><istex:document><article version="5.0" xml:lang="fr" docsubtype="fla"><item-info><jid>REVMED</jid><aid>05825020</aid><ce:pii>S0248-8663(05)82502-0</ce:pii><ce:doi>10.1016/S0248-8663(05)82502-0</ce:doi><ce:copyright type="unknown" year="1994">Éditions Scientifiques Elsevier, Paris</ce:copyright></item-info><head><ce:dochead><ce:textfn>Article Original</ce:textfn></ce:dochead><ce:title>Silicose et syndrome de Gougerot-Sjögren primitif</ce:title><ce:alt-title xml:lang="en">Silicosis and primary Sjögren's syndrome</ce:alt-title><ce:author-group><ce:author><ce:given-name>F</ce:given-name><ce:surname>Puisieux</ce:surname><ce:cross-ref refid="cor1"><ce:sup>*</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>E</ce:given-name><ce:surname>Hachulla</ce:surname></ce:author><ce:author><ce:given-name>M</ce:given-name><ce:surname>Brouillard</ce:surname></ce:author><ce:author><ce:given-name>PY</ce:given-name><ce:surname>Hatron</ce:surname></ce:author><ce:author><ce:given-name>B</ce:given-name><ce:surname>Devulder</ce:surname></ce:author><ce:affiliation id="aff1"><ce:textfn>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</ce:textfn></ce:affiliation><ce:correspondence id="cor1"><ce:label>*</ce:label><ce:text><ce:italic>Correspondance et tirés à part</ce:italic>: François Puisieux, 132, rue d'Artois, 59000 Lille.</ce:text></ce:correspondence></ce:author-group><ce:date-received day="15" month="7" year="1993"></ce:date-received><ce:date-accepted day="1" month="4" year="1994"></ce:date-accepted><ce:abstract id="ab1" class="author" xml:lang="fr"><ce:section-title>Résumé</ce:section-title><ce:abstract-sec><ce:simple-para>Les auteurs rapportent trois observations de syndrome de Gougerot-Sjögren primitif chez des mineurs de charbon atteints d'anthracosilicose. Tous les patients remplissaient les critères diagnostiques du syndrome de Gougerot-Sjögren primitif récemment établis par le groupe d'étude de la Communauté européenne. Ils avaient une xérostomie et une xérophtalmie sévères. Un patient avait une cryoglobulinémie et une polynévrite. Un autre avait un phénomène de Raynaud, des arthralgies, un purpura et une polynévrite. La capillaroscopie était normale dans les trois cas, des anticorps antinucléaires étaient détectés chez un seul patient (anticorps anti-SSA et anti-SSB). La prévalence de la sclérodermie systémique, de la polyarthrite rhumatoïde et probablement du lupus érythémateux disséminé est significativement plus élevée après exposition professionnelle prolongée à la silice. En revanche, aucun cas de syndrome de Gougerot-Sjögren primitif associé à une silicose pulmonaire n'a encore été rapporté. Les mécanismes physiopathologiques de ces associations sont mal connus.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:abstract id="ab2" class="author" xml:lang="en"><ce:section-title>Summary</ce:section-title><ce:abstract-sec><ce:simple-para>We report three cases of primary Sjögren's syndrome in silicotic coal miners. All patients fulfilled the diagnostic criteria for Sjögren's syndrome recently established by the European Community study group. One patient had cryoglobulinemia and polynevritis. Another had Raynaud's phenomenom, arthralgia, purpura and polynevritis. Capillary microscopy was normal in all the three patients. Antinuclear antibodies were detected only in one patient, who had also anti-SSa and anti-SSb antibodies. The prevalence of systemic sclerosis, rheumatoid arthritis and probably systemic lupus erythematosus is significantly higher after longstanding occupational exposure to silica. On the contrary, any case of Sjögren's syndrome was till now described in the course of pulmonary silicosis. The physiopathological mechanisms of these associations are misunderstood.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:keywords class="keyword" xml:lang="en"><ce:section-title>Keywords</ce:section-title><ce:keyword><ce:text>silicose</ce:text></ce:keyword><ce:keyword><ce:text>pneumoconiose</ce:text></ce:keyword><ce:keyword><ce:text>Gougerot-Sjögren</ce:text></ce:keyword><ce:keyword><ce:text>connectivite</ce:text></ce:keyword></ce:keywords><ce:keywords class="keyword" xml:lang="en"><ce:section-title>Keywords</ce:section-title><ce:keyword><ce:text>silicosis</ce:text></ce:keyword><ce:keyword><ce:text>pneumoconiosis</ce:text></ce:keyword><ce:keyword><ce:text>Sjögren's syndrome</ce:text></ce:keyword><ce:keyword><ce:text>connective tissue diseases</ce:text></ce:keyword></ce:keywords></head><tail><ce:bibliography><ce:section-title>Références</ce:section-title><ce:bibliography-sec><ce:bib-reference id="bib1"><ce:label>1</ce:label><sb:reference><sb:contribution langtype="iso" xml:lang="fr"><sb:authors><sb:author><ce:surname>Alcaix</ce:surname><ce:given-name>D</ce:given-name></sb:author><sb:author><ce:surname>Koeger</ce:surname><ce:given-name>AC</ce:given-name></sb:author><sb:author><ce:surname>Arnaud</ce:surname><ce:given-name>J</ce:given-name></sb:author><sb:author><ce:surname>Camus</ce:surname><ce:given-name>JP</ce:given-name></sb:author></sb:authors><sb:title><sb:maintitle>Silice et collagénoses. 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contentType="CDATA"><title>Silicose et syndrome de Gougerot-Sjögren primitif</title></titleInfo><titleInfo type="translated" lang="en"><title>Silicosis and primary Sjögren's syndrome</title></titleInfo><name type="personal"><namePart type="given">F</namePart><namePart type="family">Puisieux</namePart><affiliation>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</affiliation><description>Correspondance et tirés à part: François Puisieux, 132, rue d'Artois, 59000 Lille.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E</namePart><namePart type="family">Hachulla</namePart><affiliation>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Brouillard</namePart><affiliation>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">PY</namePart><namePart type="family">Hatron</namePart><affiliation>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">B</namePart><namePart type="family">Devulder</namePart><affiliation>Service de médecine interne, hôpital Claude-Huriez, CHRU, 59037 Lille Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1994</dateIssued><copyrightDate encoding="w3cdtf">1994</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">fre</languageTerm><languageTerm type="code" authority="rfc3066">fr</languageTerm></language><abstract lang="fr">Résumé: Les auteurs rapportent trois observations de syndrome de Gougerot-Sjögren primitif chez des mineurs de charbon atteints d'anthracosilicose. Tous les patients remplissaient les critères diagnostiques du syndrome de Gougerot-Sjögren primitif récemment établis par le groupe d'étude de la Communauté européenne. Ils avaient une xérostomie et une xérophtalmie sévères. Un patient avait une cryoglobulinémie et une polynévrite. Un autre avait un phénomène de Raynaud, des arthralgies, un purpura et une polynévrite. La capillaroscopie était normale dans les trois cas, des anticorps antinucléaires étaient détectés chez un seul patient (anticorps anti-SSA et anti-SSB). La prévalence de la sclérodermie systémique, de la polyarthrite rhumatoïde et probablement du lupus érythémateux disséminé est significativement plus élevée après exposition professionnelle prolongée à la silice. En revanche, aucun cas de syndrome de Gougerot-Sjögren primitif associé à une silicose pulmonaire n'a encore été rapporté. Les mécanismes physiopathologiques de ces associations sont mal connus.</abstract><abstract lang="en">Summary: We report three cases of primary Sjögren's syndrome in silicotic coal miners. All patients fulfilled the diagnostic criteria for Sjögren's syndrome recently established by the European Community study group. One patient had cryoglobulinemia and polynevritis. Another had Raynaud's phenomenom, arthralgia, purpura and polynevritis. Capillary microscopy was normal in all the three patients. Antinuclear antibodies were detected only in one patient, who had also anti-SSa and anti-SSb antibodies. The prevalence of systemic sclerosis, rheumatoid arthritis and probably systemic lupus erythematosus is significantly higher after longstanding occupational exposure to silica. On the contrary, any case of Sjögren's syndrome was till now described in the course of pulmonary silicosis. The physiopathological mechanisms of these associations are misunderstood.</abstract><note type="content">Section title: Article Original</note><subject lang="en"><genre>Keywords</genre><topic>silicose</topic><topic>pneumoconiose</topic><topic>Gougerot-Sjögren</topic><topic>connectivite</topic></subject><subject lang="en"><genre>Keywords</genre><topic>silicosis</topic><topic>pneumoconiosis</topic><topic>Sjögren's syndrome</topic><topic>connective tissue diseases</topic></subject><relatedItem type="host"><titleInfo><title>La Revue de medecine interne</title></titleInfo><titleInfo type="abbreviated"><title>REVMED</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1994</dateIssued></originInfo><identifier type="ISSN">0248-8663</identifier><identifier type="PII">S0248-8663(05)X8499-5</identifier><part><date>1994</date><detail type="volume"><number>15</number><caption>vol.</caption></detail><detail type="issue"><number>9</number><caption>no.</caption></detail><extent unit="issue-pages"><start>561</start><end>616</end></extent><extent unit="pages"><start>575</start><end>579</end></extent></part></relatedItem><identifier type="istex">979E14EDDCDD0139118B3CE7EDE48FF1F3BFF6CC</identifier><identifier type="ark">ark:/67375/6H6-PCKZ3PZG-W</identifier><identifier type="DOI">10.1016/S0248-8663(05)82502-0</identifier><identifier type="PII">S0248-8663(05)82502-0</identifier><identifier type="ArticleID">05825020</identifier><accessCondition type="use and reproduction" contentType="copyright">©1994 Éditions Scientifiques Elsevier, Paris</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource><recordOrigin>Éditions Scientifiques Elsevier, Paris, ©1994</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-PCKZ3PZG-W/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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