513 Heerfordt´S Syndrom in an Adolescent Boy
Introduction Heerfordt's Syndrome is characterized by bilateral uveitis, facial paralysis, fever and parotitis which is a rarely seen condition in sarcoidosis with neurological manifestations. Case report A fifteen year old boy admitted to our pediatric emergency service with fever, vomitting a...
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description | Introduction Heerfordt's Syndrome is characterized by bilateral uveitis, facial paralysis, fever and parotitis which is a rarely seen condition in sarcoidosis with neurological manifestations. Case report A fifteen year old boy admitted to our pediatric emergency service with fever, vomitting and swellings on his cheeks. Bilateral conjunctivitis, bilateral preauricular swellings, maculopapular rash on his anterior and posterior body areas and uncertain neck stiffness were detected on his physical examination. The rest of the examination was considered as in normal range. His medical history revealed an upper respiratory tract infection one week ago. Lomber puncture was performed because of patient's neck stiffness. No cell and culture growth were detected on puncture sample. During his observation, left peripheral facial paralysis was developed and bilateral uveitis was detected while his high fever was still persisting. Whole body gallium 67 scan was performed. Focal accumulations of gallium 67 in both lacrimal glands, parotid and submandibular glands(panda sign) were seen. Because of existence of uveitis, parotitis, left peripheral facial paralysis and fever, the patient was diagnosed as Heerfordt's Syndrome. Steroid (Prednisolone) treatment was started. The regressions of facial paralysis and parotid gland size were noticed after two weeks of the steroid therapy. Result This case report was chosen to take attention to a rare cause of parotitis. |
doi_str_mv | 10.1136/archdischild-2012-302724.0513 |
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Case report A fifteen year old boy admitted to our pediatric emergency service with fever, vomitting and swellings on his cheeks. Bilateral conjunctivitis, bilateral preauricular swellings, maculopapular rash on his anterior and posterior body areas and uncertain neck stiffness were detected on his physical examination. The rest of the examination was considered as in normal range. His medical history revealed an upper respiratory tract infection one week ago. Lomber puncture was performed because of patient's neck stiffness. No cell and culture growth were detected on puncture sample. During his observation, left peripheral facial paralysis was developed and bilateral uveitis was detected while his high fever was still persisting. Whole body gallium 67 scan was performed. Focal accumulations of gallium 67 in both lacrimal glands, parotid and submandibular glands(panda sign) were seen. Because of existence of uveitis, parotitis, left peripheral facial paralysis and fever, the patient was diagnosed as Heerfordt's Syndrome. Steroid (Prednisolone) treatment was started. The regressions of facial paralysis and parotid gland size were noticed after two weeks of the steroid therapy. Result This case report was chosen to take attention to a rare cause of parotitis.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2012-302724.0513</identifier><identifier>CODEN: ADCHAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><subject>Gallium ; Medical Evaluation ; Physical Examinations ; Respiratory tract ; Steroids</subject><ispartof>Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A149</ispartof><rights>2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>Copyright: 2012 (c) 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://adc.bmj.com/content/97/Suppl_2/A149.3.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://adc.bmj.com/content/97/Suppl_2/A149.3.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,23571,27924,27925,77600,77631</link.rule.ids></links><search><creatorcontrib>Arıkan, FI˙</creatorcontrib><creatorcontrib>Özkan, F</creatorcontrib><creatorcontrib>Ag˘ras, P Is¸ık</creatorcontrib><creatorcontrib>Zengin, T</creatorcontrib><creatorcontrib>Çataklı, T</creatorcontrib><creatorcontrib>Bilge, Y Dallar</creatorcontrib><title>513 Heerfordt´S Syndrom in an Adolescent Boy</title><title>Archives of disease in childhood</title><addtitle>Arch Dis Child</addtitle><description>Introduction Heerfordt's Syndrome is characterized by bilateral uveitis, facial paralysis, fever and parotitis which is a rarely seen condition in sarcoidosis with neurological manifestations. Case report A fifteen year old boy admitted to our pediatric emergency service with fever, vomitting and swellings on his cheeks. Bilateral conjunctivitis, bilateral preauricular swellings, maculopapular rash on his anterior and posterior body areas and uncertain neck stiffness were detected on his physical examination. The rest of the examination was considered as in normal range. His medical history revealed an upper respiratory tract infection one week ago. Lomber puncture was performed because of patient's neck stiffness. No cell and culture growth were detected on puncture sample. During his observation, left peripheral facial paralysis was developed and bilateral uveitis was detected while his high fever was still persisting. Whole body gallium 67 scan was performed. Focal accumulations of gallium 67 in both lacrimal glands, parotid and submandibular glands(panda sign) were seen. Because of existence of uveitis, parotitis, left peripheral facial paralysis and fever, the patient was diagnosed as Heerfordt's Syndrome. Steroid (Prednisolone) treatment was started. The regressions of facial paralysis and parotid gland size were noticed after two weeks of the steroid therapy. Result This case report was chosen to take attention to a rare cause of parotitis.</description><subject>Gallium</subject><subject>Medical Evaluation</subject><subject>Physical Examinations</subject><subject>Respiratory tract</subject><subject>Steroids</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpN0N1KwzAUwPEgCs7pOxTEy8yk-WhyuRV1wpzC5vAuZEnKWrd2Jh249_IJfDJTKuLVgcOP5PAH4AajEcaE32pvNrYMZlNuLUwRTiFBaZbSEWKYnIABplzEPaWnYIAQIlAKIc7BRQgViloIMgAw0mTqnC8ab9vvr0WyONbWN7ukrBNdJ2PbbF0wrm6TSXO8BGeF3gZ39TuH4PX-bplP4ez54TEfz-AaY0ah4JJkXHLiJJfSCcnTtdU4tdrGA7UoNDGUMCMlskZIFJEtmGXU8sIZZ8kQXPfv7n3zcXChVVVz8HX8UmERD2ecYhoV7FUZWvep9r7caX9U2r8rnpGMqfkqV2_LlxV9yudqEr3o_XpX_WmMVBdT_Y-pupiqj6m6mOQHUC9pWg</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Arıkan, FI˙</creator><creator>Özkan, F</creator><creator>Ag˘ras, P Is¸ık</creator><creator>Zengin, T</creator><creator>Çataklı, T</creator><creator>Bilge, Y Dallar</creator><general>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>201210</creationdate><title>513 Heerfordt´S Syndrom in an Adolescent Boy</title><author>Arıkan, FI˙ ; Özkan, F ; Ag˘ras, P Is¸ık ; Zengin, T ; Çataklı, T ; Bilge, Y Dallar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1154-869376963e9699e8962bda12dad027a8fa3c435c990dc890699df5d54d6feced3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Gallium</topic><topic>Medical Evaluation</topic><topic>Physical Examinations</topic><topic>Respiratory tract</topic><topic>Steroids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arıkan, FI˙</creatorcontrib><creatorcontrib>Özkan, F</creatorcontrib><creatorcontrib>Ag˘ras, P Is¸ık</creatorcontrib><creatorcontrib>Zengin, T</creatorcontrib><creatorcontrib>Çataklı, T</creatorcontrib><creatorcontrib>Bilge, Y Dallar</creatorcontrib><collection>Istex</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Education</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Archives of disease in childhood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arıkan, FI˙</au><au>Özkan, F</au><au>Ag˘ras, P Is¸ık</au><au>Zengin, T</au><au>Çataklı, T</au><au>Bilge, Y Dallar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>513 Heerfordt´S Syndrom in an Adolescent Boy</atitle><jtitle>Archives of disease in childhood</jtitle><addtitle>Arch Dis Child</addtitle><date>2012-10</date><risdate>2012</risdate><volume>97</volume><issue>Suppl 2</issue><spage>A149</spage><pages>A149-</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><coden>ADCHAK</coden><abstract>Introduction Heerfordt's Syndrome is characterized by bilateral uveitis, facial paralysis, fever and parotitis which is a rarely seen condition in sarcoidosis with neurological manifestations. Case report A fifteen year old boy admitted to our pediatric emergency service with fever, vomitting and swellings on his cheeks. Bilateral conjunctivitis, bilateral preauricular swellings, maculopapular rash on his anterior and posterior body areas and uncertain neck stiffness were detected on his physical examination. The rest of the examination was considered as in normal range. His medical history revealed an upper respiratory tract infection one week ago. Lomber puncture was performed because of patient's neck stiffness. No cell and culture growth were detected on puncture sample. During his observation, left peripheral facial paralysis was developed and bilateral uveitis was detected while his high fever was still persisting. Whole body gallium 67 scan was performed. Focal accumulations of gallium 67 in both lacrimal glands, parotid and submandibular glands(panda sign) were seen. Because of existence of uveitis, parotitis, left peripheral facial paralysis and fever, the patient was diagnosed as Heerfordt's Syndrome. Steroid (Prednisolone) treatment was started. The regressions of facial paralysis and parotid gland size were noticed after two weeks of the steroid therapy. Result This case report was chosen to take attention to a rare cause of parotitis.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</pub><doi>10.1136/archdischild-2012-302724.0513</doi></addata></record> |
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title | 513 Heerfordt´S Syndrom in an Adolescent Boy |
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