Recurrent aphthous ulcers in Fanconi's anaemia: a case report
Identifieur interne : 006144 ( Istex/Corpus ); précédent : 006143; suivant : 006145Recurrent aphthous ulcers in Fanconi's anaemia: a case report
Auteurs : Feyza Otan ; Gokhan Açikgöz ; Umur Sakallio Lu ; Burcu ÖzkanSource :
- International Journal of Paediatric Dentistry [ 0960-7439 ] ; 2004-05.
English descriptors
- KwdEn :
- Abnormality, Aggressive periodontitis, American journal, Anaemia, Anemia, Aphthous, Aphthous lesion, Aphthous lesions, Aphthous ulcerations, Aplastic, Aplastic anaemia, Aplastic anemia, Apthous stomatitis, Autosomal recessive disorder, Blood counts, Bspd, Case report, Congenital malformations, Dentistry, Fanconi, Fanconi anemia, Growth retardation, Iapd, Implant surgery, International journal, Last blood transfusion, Lesion, Malformation, Malignancy, Ndings, Oral mucosa, Oral ulcerations, Paediatric, Paediatric dentistry, Pediatric, Periodontal, Periodontal examination, Periodontology, Peripheral blood smear, Pfapa, Pfapa syndrome, Physical abnormalities, Physical examination, Recurrent aphthous ulcers, Severe anaemia, Short stature, Squamous cell carcinoma, Transfusion, Ulceration.
- Teeft :
- Abnormality, Aggressive periodontitis, American journal, Anaemia, Anemia, Aphthous, Aphthous lesion, Aphthous lesions, Aphthous ulcerations, Aplastic, Aplastic anaemia, Aplastic anemia, Apthous stomatitis, Autosomal recessive disorder, Blood counts, Bspd, Case report, Congenital malformations, Dentistry, Fanconi, Fanconi anemia, Growth retardation, Iapd, Implant surgery, International journal, Last blood transfusion, Lesion, Malformation, Malignancy, Ndings, Oral mucosa, Oral ulcerations, Paediatric, Paediatric dentistry, Pediatric, Periodontal, Periodontal examination, Periodontology, Peripheral blood smear, Pfapa, Pfapa syndrome, Physical abnormalities, Physical examination, Recurrent aphthous ulcers, Severe anaemia, Short stature, Squamous cell carcinoma, Transfusion, Ulceration.
Abstract
Summary. Fanconi's anaemia (FA) is an autosomal recessive disorder that is clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, and an increased predisposition to malignancies. Patients with FA often present with bleeding and infection, which are symptoms related to thrombocytopenia and neutropenia. There are few reports of the oral manifestations of FA. We describe oral aphthous ulcerations in two siblings with FA. There was a rapid improvement and healing of ulcers after blood transfusions and increased haemoglobin levels. This may support the role of severe anaemia in oral ulcerations.
Url:
DOI: 10.1111/j.1365-263X.2004.00549.x
Links to Exploration step
ISTEX:C3D129ECF3BD480CCF0265A29F8637D4BE1FA298Le document en format XML
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Fanconi's anaemia (FA) is an autosomal recessive disorder that is clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, and an increased predisposition to malignancies. Patients with FA often present with bleeding and infection, which are symptoms related to thrombocytopenia and neutropenia. There are few reports of the oral manifestations of FA. We describe oral aphthous ulcerations in two siblings with FA. There was a rapid improvement and healing of ulcers after blood transfusions and increased haemoglobin levels. 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Fanconi's anaemia (FA) is an autosomal recessive disorder that is clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, and an increased predisposition to malignancies. Patients with FA often present with bleeding and infection, which are symptoms related to thrombocytopenia and neutropenia. There are few reports of the oral manifestations of FA. We describe oral aphthous ulcerations in two siblings with FA. There was a rapid improvement and healing of ulcers after blood transfusions and increased haemoglobin levels. 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[19]</json:string><json:string>[19]</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-6MHDVKJC-1</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - pediatrics</json:string><json:string>2 - dentistry, oral surgery & medicine</json:string></wos><scienceMetrix><json:string>1 - health sciences</json:string><json:string>2 - clinical medicine</json:string><json:string>3 - dentistry</json:string></scienceMetrix><scopus><json:string>1 - Health Sciences</json:string><json:string>2 - Dentistry</json:string><json:string>3 - General Dentistry</json:string></scopus></categories><publicationDate>2004</publicationDate><copyrightDate>2004</copyrightDate><doi><json:string>10.1111/j.1365-263X.2004.00549.x</json:string></doi><id>C3D129ECF3BD480CCF0265A29F8637D4BE1FA298</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/C3D129ECF3BD480CCF0265A29F8637D4BE1FA298/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/C3D129ECF3BD480CCF0265A29F8637D4BE1FA298/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/C3D129ECF3BD480CCF0265A29F8637D4BE1FA298/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main">Recurrent aphthous ulcers in Fanconi's anaemia: a case report</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Blackwell Science Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2004-05"></date></publicationStmt><notesStmt><note type="content-type" subtype="case-report" source="caseStudy" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-29919SZJ-6">case-report</note><note type="publication-type" subtype="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note></notesStmt><sourceDesc><biblStruct type="case-report"><analytic><title level="a" type="main">Recurrent aphthous ulcers in Fanconi's anaemia: a case report</title><title level="a" type="short">Recurrent aphthous ulcers in Fanconi's anaemia</title><author xml:id="author-0000"><persName><forename type="first">Feyza</forename><surname>Otan</surname></persName><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey<address><country key="TR"></country></address></affiliation></author><author xml:id="author-0001" role="corresp"><persName><forename type="first">Gokhan</forename><surname>Açikgöz</surname></persName><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey<address><country key="TR"></country></address></affiliation><affiliation>G. Açikgöz, Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, 55139 Kurupelit‐Samsun, Turkey. E‐mail: gacikgoz@omu.edu.tr</affiliation></author><author xml:id="author-0002"><persName><forename type="first">Umur</forename><surname>Sakallioǧlu</surname></persName><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey<address><country key="TR"></country></address></affiliation></author><author xml:id="author-0003"><persName><forename type="first">Burcu</forename><surname>Özkan</surname></persName><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey<address><country key="TR"></country></address></affiliation></author><idno type="istex">C3D129ECF3BD480CCF0265A29F8637D4BE1FA298</idno><idno type="ark">ark:/67375/WNG-6MHDVKJC-1</idno><idno type="DOI">10.1111/j.1365-263X.2004.00549.x</idno><idno type="unit">IPD549</idno><idno type="toTypesetVersion">file:IPD.IPD549.pdf</idno></analytic><monogr><title level="j" type="main">International Journal of Paediatric Dentistry</title><title level="j" type="alt">INTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY</title><idno type="pISSN">0960-7439</idno><idno type="eISSN">1365-263X</idno><idno type="book-DOI">10.1111/(ISSN)1365-263X</idno><idno type="book-part-DOI">10.1111/ipd.2004.14.issue-3</idno><idno type="product">IPD</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">14</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="214">214</biblScope><biblScope unit="page" to="217">217</biblScope><biblScope unit="page-count">4</biblScope><publisher>Blackwell Science Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2004-05"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><p><hi rend="bold">Summary. </hi> Fanconi's anaemia (FA) is an autosomal recessive disorder that is clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, and an increased predisposition to malignancies. Patients with FA often present with bleeding and infection, which are symptoms related to thrombocytopenia and neutropenia. There are few reports of the oral manifestations of FA. We describe oral aphthous ulcerations in two siblings with FA. There was a rapid improvement and healing of ulcers after blood transfusions and increased haemoglobin levels. This may support the role of severe anaemia in oral ulcerations.</p></abstract><textClass><keywords rend="tocHeading1"><term>CASE REPORTS</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/C3D129ECF3BD480CCF0265A29F8637D4BE1FA298/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Science Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1365-263X</doi><issn type="print">0960-7439</issn><issn type="electronic">1365-263X</issn><idGroup><id type="product" value="IPD"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="INTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY">International Journal of Paediatric Dentistry</title></titleGroup></publicationMeta><publicationMeta level="part" position="05003"><doi origin="wiley">10.1111/ipd.2004.14.issue-3</doi><numberingGroup><numbering type="journalVolume" number="14">14</numbering><numbering type="journalIssue" number="3">3</numbering></numberingGroup><coverDate startDate="2004-05">May 2004</coverDate></publicationMeta><publicationMeta level="unit" type="caseStudy" position="10" status="forIssue"><doi origin="wiley">10.1111/j.1365-263X.2004.00549.x</doi><idGroup><id type="unit" value="IPD549"></id></idGroup><countGroup><count type="pageTotal" number="4"></count></countGroup><titleGroup><title type="tocHeading1">CASE REPORTS</title></titleGroup><eventGroup><event type="firstOnline" date="2004-05-10"></event><event type="publishedOnlineFinalForm" date="2004-05-10"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-06"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-30"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-24"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="214">214</numbering><numbering type="pageLast" number="217">217</numbering></numberingGroup><correspondenceTo> G. Açikgöz, Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, 55139 Kurupelit‐Samsun, Turkey. E‐mail: <email>gacikgoz@omu.edu.tr</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:IPD.IPD549.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="3"></count><count type="tableTotal" number="0"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="19"></count><count type="wordTotal" number="1891"></count></countGroup><titleGroup><title type="main">Recurrent aphthous ulcers in Fanconi's anaemia: a case report</title><title type="shortAuthors"><i>F. Otan</i> et al.</title><title type="short"><i>Recurrent aphthous ulcers in Fanconi's anaemia</i></title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>Feyza</givenNames><familyName>Otan</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1" corresponding="yes"><personName><givenNames>Gokhan</givenNames><familyName>Açikgöz</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a1"><personName><givenNames>Umur</givenNames><familyName>Sakallioǧlu</familyName></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a1"><personName><givenNames>Burcu</givenNames><familyName>Özkan</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="TR"><unparsedAffiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><p><b>Summary. </b> Fanconi's anaemia (FA) is an autosomal recessive disorder that is clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, and an increased predisposition to malignancies. Patients with FA often present with bleeding and infection, which are symptoms related to thrombocytopenia and neutropenia. There are few reports of the oral manifestations of FA. We describe oral aphthous ulcerations in two siblings with FA. There was a rapid improvement and healing of ulcers after blood transfusions and increased haemoglobin levels. This may support the role of severe anaemia in oral ulcerations.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Recurrent aphthous ulcers in Fanconi's anaemia: a case report</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Recurrent aphthous ulcers in Fanconi's anaemia</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Recurrent aphthous ulcers in Fanconi's anaemia: a case report</title></titleInfo><name type="personal"><namePart type="given">Feyza</namePart><namePart type="family">Otan</namePart><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Gokhan</namePart><namePart type="family">Açikgöz</namePart><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey</affiliation><affiliation>E-mail: gacikgoz@omu.edu.tr</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Umur</namePart><namePart type="family">Sakallioǧlu</namePart><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Burcu</namePart><namePart type="family">Özkan</namePart><affiliation>Ondokuz Mayis University, Faculty of Dentistry, Department of Periodontology, Kurupelit‐Samsun, Turkey</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="case-report" displayLabel="caseStudy" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-29919SZJ-6">case-report</genre><originInfo><publisher>Blackwell Science Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2004-05</dateIssued><copyrightDate encoding="w3cdtf">2004</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">3</extent><extent unit="tables">0</extent><extent unit="formulas">0</extent><extent unit="references">19</extent><extent unit="words">1891</extent></physicalDescription><abstract>Summary. Fanconi's anaemia (FA) is an autosomal recessive disorder that is clinically characterized by aplastic anaemia, congenital malformations of the renal, cardiac, skeletal and skin structures, and an increased predisposition to malignancies. Patients with FA often present with bleeding and infection, which are symptoms related to thrombocytopenia and neutropenia. There are few reports of the oral manifestations of FA. We describe oral aphthous ulcerations in two siblings with FA. There was a rapid improvement and healing of ulcers after blood transfusions and increased haemoglobin levels. This may support the role of severe anaemia in oral ulcerations.</abstract><relatedItem type="host"><titleInfo><title>International Journal of Paediatric Dentistry</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><identifier type="ISSN">0960-7439</identifier><identifier type="eISSN">1365-263X</identifier><identifier type="DOI">10.1111/(ISSN)1365-263X</identifier><identifier type="PublisherID">IPD</identifier><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>14</number></detail><detail type="issue"><caption>no.</caption><number>3</number></detail><extent unit="pages"><start>214</start><end>217</end><total>4</total></extent></part></relatedItem><identifier type="istex">C3D129ECF3BD480CCF0265A29F8637D4BE1FA298</identifier><identifier type="ark">ark:/67375/WNG-6MHDVKJC-1</identifier><identifier type="DOI">10.1111/j.1365-263X.2004.00549.x</identifier><identifier type="ArticleID">IPD549</identifier><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>Blackwell Science Ltd</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/C3D129ECF3BD480CCF0265A29F8637D4BE1FA298/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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