Pilomatricomas in Turner Syndrome
Identifieur interne : 002547 ( Istex/Corpus ); précédent : 002546; suivant : 002548Pilomatricomas in Turner Syndrome
Auteurs : Simon Wood ; Dai Nguyen ; Kim Hutton ; William DicksonSource :
- Pediatric Dermatology [ 0736-8046 ] ; 2008-07.
Abstract
Abstract: Pilomatricomas are benign, cutaneous tumors of the hair matrix cells, which present predominantly in childhood. Although usually an isolated finding, they have been described in association with several inherited conditions. We report a 10‐year‐old girl with Turner syndrome who has two pilomatricomas, including one giant tumor. In combination with a previous report of pilomatricoma in two patients with Turner syndrome, our observation indicates that it is likely a real, although uncommon, association of pilomatricomas with Turner syndrome exists.. This apparent predisposition may be etiologically related to the abnormalities of hair‐bearing skin observed in Turner syndrome. Doctors involved in the diagnosis and management of cutaneous masses in children should be aware of this association.
Url:
DOI: 10.1111/j.1525-1470.2008.00732.x
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ISTEX:5162F3CA873FC88D8C291FC188727241DAA03607Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Pilomatricomas in Turner Syndrome</title><author><name sortKey="Wood, Simon" sort="Wood, Simon" uniqKey="Wood S" first="Simon" last="Wood">Simon Wood</name><affiliation><mods:affiliation>Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, UK</mods:affiliation></affiliation></author><author><name sortKey="Nguyen, Dai" sort="Nguyen, Dai" uniqKey="Nguyen D" first="Dai" last="Nguyen">Dai Nguyen</name><affiliation><mods:affiliation>Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, UK</mods:affiliation></affiliation></author><author><name sortKey="Hutton, Kim" sort="Hutton, Kim" uniqKey="Hutton K" first="Kim" last="Hutton">Kim Hutton</name><affiliation><mods:affiliation>Department of Pediatric Surgery, University Hospital of Wales, Cardiff, UK</mods:affiliation></affiliation></author><author><name sortKey="Dickson, William" sort="Dickson, William" uniqKey="Dickson W" first="William" last="Dickson">William Dickson</name><affiliation><mods:affiliation>Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, UK</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:5162F3CA873FC88D8C291FC188727241DAA03607</idno><date when="2008" year="2008">2008</date><idno type="doi">10.1111/j.1525-1470.2008.00732.x</idno><idno type="url">https://api.istex.fr/document/5162F3CA873FC88D8C291FC188727241DAA03607/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">002547</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">002547</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main">Pilomatricomas in Turner Syndrome</title><author><name sortKey="Wood, Simon" sort="Wood, Simon" uniqKey="Wood S" first="Simon" last="Wood">Simon Wood</name><affiliation><mods:affiliation>Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, UK</mods:affiliation></affiliation></author><author><name sortKey="Nguyen, Dai" sort="Nguyen, Dai" uniqKey="Nguyen D" first="Dai" last="Nguyen">Dai Nguyen</name><affiliation><mods:affiliation>Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, UK</mods:affiliation></affiliation></author><author><name sortKey="Hutton, Kim" sort="Hutton, Kim" uniqKey="Hutton K" first="Kim" last="Hutton">Kim Hutton</name><affiliation><mods:affiliation>Department of Pediatric Surgery, University Hospital of Wales, Cardiff, UK</mods:affiliation></affiliation></author><author><name sortKey="Dickson, William" sort="Dickson, William" uniqKey="Dickson W" first="William" last="Dickson">William Dickson</name><affiliation><mods:affiliation>Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, UK</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Pediatric Dermatology</title><title level="j" type="alt">PEDIATRIC DERMATOLOGY</title><idno type="ISSN">0736-8046</idno><idno type="eISSN">1525-1470</idno><imprint><biblScope unit="vol">25</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="449">449</biblScope><biblScope unit="page" to="451">451</biblScope><biblScope unit="page-count">3</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2008-07">2008-07</date></imprint><idno type="ISSN">0736-8046</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0736-8046</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract">Abstract: Pilomatricomas are benign, cutaneous tumors of the hair matrix cells, which present predominantly in childhood. 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Although usually an isolated finding, they have been described in association with several inherited conditions. We report a 10‐year‐old girl with Turner syndrome who has two pilomatricomas, including one giant tumor. In combination with a previous report of pilomatricoma in two patients with Turner syndrome, our observation indicates that it is likely a real, although uncommon, association of pilomatricomas with Turner syndrome exists.. This apparent predisposition may be etiologically related to the abnormalities of hair‐bearing skin observed in Turner syndrome. Doctors involved in the diagnosis and management of cutaneous masses in children should be aware of this association.</p></abstract><textClass><classCode scheme="tocHeading1">CASE REPORTS</classCode></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/5162F3CA873FC88D8C291FC188727241DAA03607/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 Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1525-1470</doi><issn type="print">0736-8046</issn><issn type="electronic">1525-1470</issn><idGroup><id type="product" value="PDE"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="PEDIATRIC DERMATOLOGY">Pediatric Dermatology</title></titleGroup></publicationMeta><publicationMeta level="part" position="07004"><doi origin="wiley">10.1111/pde.2008.25.issue-4</doi><numberingGroup><numbering type="journalVolume" number="25">25</numbering><numbering type="journalIssue" number="4">4</numbering></numberingGroup><coverDate startDate="2008-07">July/August 2008</coverDate></publicationMeta><publicationMeta level="unit" type="caseStudy" position="5" status="forIssue"><doi origin="wiley">10.1111/j.1525-1470.2008.00732.x</doi><idGroup><id type="unit" value="PDE732"></id></idGroup><countGroup><count type="pageTotal" number="3"></count></countGroup><titleGroup><title type="tocHeading1">CASE REPORTS</title></titleGroup><copyright>© 2008 The Authors. Journal compilation © 2008 Wiley Periodicals, Inc.</copyright><eventGroup><event type="firstOnline" date="2008-08-07"></event><event type="publishedOnlineFinalForm" date="2008-08-07"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-04"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-06"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-11-03"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="449">449</numbering><numbering type="pageLast" number="451">451</numbering></numberingGroup><correspondenceTo>Address correspondence to Simon Wood, M.R.C.S., Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, United Kingdom, SA6 6NL, or e‐mail: <email>siwood@doctors.org.uk</email>.</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:PDE.PDE732.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="2"></count><count type="tableTotal" number="0"></count></countGroup><titleGroup><title type="main">Pilomatricomas in Turner Syndrome</title><title type="shortAuthors">Wood et al</title><title type="short">Pilomatricomas in Turner Syndrome</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>Simon</givenNames><familyName>Wood</familyName><degrees>M.R.C.S.</degrees></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>Dai</givenNames><familyName>Nguyen</familyName><degrees>M.R.C.S.</degrees></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a2"><personName><givenNames>Kim</givenNames><familyName>Hutton</familyName><degrees>F.R.C.S.</degrees></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a1"><personName><givenNames> William</givenNames><familyName>Dickson</familyName><degrees>F.R.C.S.</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="GB"><unparsedAffiliation>Department of Burns and Plastic Surgery, Morriston Hospital, Swansea, UK</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="GB"><unparsedAffiliation>Department of Pediatric Surgery, University Hospital of Wales, Cardiff, UK</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><p><b>Abstract: </b> Pilomatricomas are benign, cutaneous tumors of the hair matrix cells, which present predominantly in childhood. Although usually an isolated finding, they have been described in association with several inherited conditions. We report a 10‐year‐old girl with Turner syndrome who has two pilomatricomas, including one giant tumor. In combination with a previous report of pilomatricoma in two patients with Turner syndrome, our observation indicates that it is likely a real, although uncommon, association of pilomatricomas with Turner syndrome exists.. This apparent predisposition may be etiologically related to the abnormalities of hair‐bearing skin observed in Turner syndrome. 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Although usually an isolated finding, they have been described in association with several inherited conditions. We report a 10‐year‐old girl with Turner syndrome who has two pilomatricomas, including one giant tumor. In combination with a previous report of pilomatricoma in two patients with Turner syndrome, our observation indicates that it is likely a real, although uncommon, association of pilomatricomas with Turner syndrome exists.. This apparent predisposition may be etiologically related to the abnormalities of hair‐bearing skin observed in Turner syndrome. Doctors involved in the diagnosis and management of cutaneous masses in children should be aware of this association.</abstract><relatedItem type="host"><titleInfo><title>Pediatric Dermatology</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0736-8046</identifier><identifier type="eISSN">1525-1470</identifier><identifier type="DOI">10.1111/(ISSN)1525-1470</identifier><identifier type="PublisherID">PDE</identifier><part><date>2008</date><detail type="volume"><caption>vol.</caption><number>25</number></detail><detail type="issue"><caption>no.</caption><number>4</number></detail><extent unit="pages"><start>449</start><end>451</end><total>3</total></extent></part></relatedItem><identifier type="istex">5162F3CA873FC88D8C291FC188727241DAA03607</identifier><identifier type="DOI">10.1111/j.1525-1470.2008.00732.x</identifier><identifier type="ArticleID">PDE732</identifier><accessCondition type="use and reproduction" contentType="copyright">© 2008 The Authors. 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