Behçet’s disease in Brazilian patients: demographic and clinical features
The aim of this study was to determine the demographic and clinical characteristics in patients diagnosed with Behçet’s disease (BD) in Brazil. We performed a retrospective review of all the patients’ records with BD diagnosed from 1988 to 2010 in the Rheumatology Department at the State University...
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| Veröffentlicht in: | Rheumatology international 2012-07, Vol.32 (7), p.2063-2067 |
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| container_title | Rheumatology international |
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| creator | Sachetto, Zoraida Mahayri, Nazira Ferraz, Rosemeire Holanda Costallat, Lilian Teresa Lavras Bertolo, Manoel Barros |
| description | The aim of this study was to determine the demographic and clinical characteristics in patients diagnosed with Behçet’s disease (BD) in Brazil. We performed a retrospective review of all the patients’ records with BD diagnosed from 1988 to 2010 in the Rheumatology Department at the State University of Campinas (UNICAMP). All patients had to fulfill the International Study Group for Behçet’s disease diagnostic criteria. Eighty-seven patients were included in the study. The female/male ratio was 1.18:1, and the mean age at the onset of the disease onset was 28.03 ± 7.57 years. Oral aphthosis was the most frequent manifestation (100%). Genital aphthosis was also frequent (77%), followed by pseudofolliculitis (47.67%). Ocular symptoms were present in 80% and neurological manifestations in 31.03% of the patients. Arthralgia was reported in 31.03% and arthritis in 13.79% of the cases. Vascular involvement was seen in 13.95% of the patients. Only 1.14% had gastrointestinal involvement. This series, from a South American country, showed a similar general pattern of the BD to those found in different endemic areas in the world, with a high frequency of ocular and neurological manifestations. |
| doi_str_mv | 10.1007/s00296-011-1921-z |
| format | Article |
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We performed a retrospective review of all the patients’ records with BD diagnosed from 1988 to 2010 in the Rheumatology Department at the State University of Campinas (UNICAMP). All patients had to fulfill the International Study Group for Behçet’s disease diagnostic criteria. Eighty-seven patients were included in the study. The female/male ratio was 1.18:1, and the mean age at the onset of the disease onset was 28.03 ± 7.57 years. Oral aphthosis was the most frequent manifestation (100%). Genital aphthosis was also frequent (77%), followed by pseudofolliculitis (47.67%). Ocular symptoms were present in 80% and neurological manifestations in 31.03% of the patients. Arthralgia was reported in 31.03% and arthritis in 13.79% of the cases. Vascular involvement was seen in 13.95% of the patients. Only 1.14% had gastrointestinal involvement. This series, from a South American country, showed a similar general pattern of the BD to those found in different endemic areas in the world, with a high frequency of ocular and neurological manifestations.</description><identifier>ISSN: 0172-8172</identifier><identifier>EISSN: 1437-160X</identifier><identifier>DOI: 10.1007/s00296-011-1921-z</identifier><identifier>PMID: 21479883</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Adult ; Behcet Syndrome - diagnosis ; Behcet Syndrome - epidemiology ; Brazil - epidemiology ; Female ; Humans ; Male ; Medicine ; Medicine & Public Health ; Original Article ; Prevalence ; Retrospective Studies ; Rheumatology ; Young Adult</subject><ispartof>Rheumatology international, 2012-07, Vol.32 (7), p.2063-2067</ispartof><rights>Springer-Verlag 2011</rights><rights>Springer-Verlag 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353z-a26ca0967296e472f821bf88ef0a52d58b06cf8fb0334b36c7393e252fb5edf43</citedby><cites>FETCH-LOGICAL-c353z-a26ca0967296e472f821bf88ef0a52d58b06cf8fb0334b36c7393e252fb5edf43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00296-011-1921-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00296-011-1921-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,41486,42555,51317</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21479883$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sachetto, Zoraida</creatorcontrib><creatorcontrib>Mahayri, Nazira</creatorcontrib><creatorcontrib>Ferraz, Rosemeire Holanda</creatorcontrib><creatorcontrib>Costallat, Lilian Teresa Lavras</creatorcontrib><creatorcontrib>Bertolo, Manoel Barros</creatorcontrib><title>Behçet’s disease in Brazilian patients: demographic and clinical features</title><title>Rheumatology international</title><addtitle>Rheumatol Int</addtitle><addtitle>Rheumatol Int</addtitle><description>The aim of this study was to determine the demographic and clinical characteristics in patients diagnosed with Behçet’s disease (BD) in Brazil. 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This series, from a South American country, showed a similar general pattern of the BD to those found in different endemic areas in the world, with a high frequency of ocular and neurological manifestations.</description><subject>Adult</subject><subject>Behcet Syndrome - diagnosis</subject><subject>Behcet Syndrome - epidemiology</subject><subject>Brazil - epidemiology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Original Article</subject><subject>Prevalence</subject><subject>Retrospective Studies</subject><subject>Rheumatology</subject><subject>Young Adult</subject><issn>0172-8172</issn><issn>1437-160X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kEtOwzAQhi0EoqVwADYoEhs2AT-S2GFHK15SJTYgsYscZ9y6ygs7WdAV1-AEHISbcBJcWhBCYuORNd_8M_oQOiT4lGDMzxzGNE1CTEhIUkrC5RYakojxkCT4cRsNMeE0FP4ZoD3nFtj_kwTvogElEU-FYEM0HcP8_Q26j5dXFxTGgXQQmDoYW7k0pZF10MrOQN2586CAqplZ2c6NCmRdBKo0tVGyDDTIrrfg9tGOlqWDg00doYery_vJTTi9u76dXExDxWK2DCVNlMRpwv3xEHGqBSW5FgI0ljEtYpHjRGmhc8xYlLNEcZYyoDHVeQyFjtgInaxzW9s89eC6rDJOQVnKGpreZQRTyrhgHHv0-A-6aHpb--u-KELilFBPkTWlbOOcBZ211lTSPnsoW6nO1qozrzpbqc6WfuZok9znFRQ_E99uPUDXgPOtegb29-r_Uj8BDGuKdw</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Sachetto, Zoraida</creator><creator>Mahayri, Nazira</creator><creator>Ferraz, Rosemeire Holanda</creator><creator>Costallat, Lilian Teresa Lavras</creator><creator>Bertolo, Manoel Barros</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>201207</creationdate><title>Behçet’s disease in Brazilian patients: demographic and clinical features</title><author>Sachetto, Zoraida ; 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We performed a retrospective review of all the patients’ records with BD diagnosed from 1988 to 2010 in the Rheumatology Department at the State University of Campinas (UNICAMP). All patients had to fulfill the International Study Group for Behçet’s disease diagnostic criteria. Eighty-seven patients were included in the study. The female/male ratio was 1.18:1, and the mean age at the onset of the disease onset was 28.03 ± 7.57 years. Oral aphthosis was the most frequent manifestation (100%). Genital aphthosis was also frequent (77%), followed by pseudofolliculitis (47.67%). Ocular symptoms were present in 80% and neurological manifestations in 31.03% of the patients. Arthralgia was reported in 31.03% and arthritis in 13.79% of the cases. Vascular involvement was seen in 13.95% of the patients. Only 1.14% had gastrointestinal involvement. 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| subjects | Adult Behcet Syndrome - diagnosis Behcet Syndrome - epidemiology Brazil - epidemiology Female Humans Male Medicine Medicine & Public Health Original Article Prevalence Retrospective Studies Rheumatology Young Adult |
| title | Behçet’s disease in Brazilian patients: demographic and clinical features |
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