Subcutaneous sarcoidosis—clinicopathological study of 10 cases
Identifieur interne : 002366 ( Istex/Corpus ); précédent : 002365; suivant : 002367Subcutaneous sarcoidosis—clinicopathological study of 10 cases
Auteurs : J. Marcoval ; J. Ma A ; A. Moreno ; J. PeyriSource :
- British Journal of Dermatology [ 0007-0963 ] ; 2005-10.
Abstract
Background Subcutaneous sarcoidosis is a specific cutaneous lesion of sarcoidosis that is rarely reported. Objective Our purpose was to analyse the clinicopathological features of 10 patients with subcutaneous sarcoidosis and its relationship with the systemic features of the disease. Patients and methods The patients with systemic sarcoidosis, diagnosed from 1974 to 2002 at a university hospital in Barcelona, Spain, who developed subcutaneous involvement, were included in the study. The diagnosis of systemic sarcoidosis was made according to conventional criteria. All the patients were monitored prospectively at the sarcoidosis clinic of the hospital. Skin biopsies were performed when granulomatous cutaneous involvement was suspected clinically. Results Granulomatous cutaneous involvement was demonstrated in 85 of 480 patients with systemic sarcoidosis. In 10 of these 85 patients subcutaneous sarcoidosis was diagnosed (11·8%). The lesions were most frequently located in the extremities, involving the forearms in nine patients. Indurated linear bands from the elbow to the hand were observed in five patients. In all of our patients the subcutaneous nodules appeared at the beginning of the disease. In six patients, the nodules remitted spontaneously in less than 2 years. In two cases foreign particles were detected under polarized light. Conclusions Subcutaneous sarcoidosis is a quite uniform clinicopathological entity usually appearing at the beginning of the disease. It usually heralds forms of sarcoidosis with nonsevere systemic involvement and is not associated with chronic fibrotic disease.
Url:
DOI: 10.1111/j.1365-2133.2005.06815.x
Links to Exploration step
ISTEX:84FA235B9B5DBFBDFDBCBEAAF3C7091160D2ED7ELe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
<author><name sortKey="Marcoval, J" sort="Marcoval, J" uniqKey="Marcoval J" first="J." last="Marcoval">J. Marcoval</name>
<affiliation><mods:affiliation>Departments of Dermatology, Internal Medicine</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Ma A, J" sort="Ma A, J" uniqKey="Ma A J" first="J." last="Ma A">J. Ma A</name>
<affiliation><mods:affiliation>Departments of Dermatology, Internal Medicine</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Moreno, A" sort="Moreno, A" uniqKey="Moreno A" first="A." last="Moreno">A. Moreno</name>
<affiliation><mods:affiliation>Pathology, Hospital de Bellvitge, c/Feixa Llarga s/n, Hospitalet de Llobregat, University of Barcelona, 08907 Barcelona, Spain</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Peyri, J" sort="Peyri, J" uniqKey="Peyri J" first="J." last="Peyri">J. Peyri</name>
<affiliation><mods:affiliation>Departments of Dermatology, Internal Medicine</mods:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:84FA235B9B5DBFBDFDBCBEAAF3C7091160D2ED7E</idno>
<date when="2005" year="2005">2005</date>
<idno type="doi">10.1111/j.1365-2133.2005.06815.x</idno>
<idno type="url">https://api.istex.fr/ark:/67375/WNG-P9N0TSXN-V/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002366</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">002366</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main">Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
<author><name sortKey="Marcoval, J" sort="Marcoval, J" uniqKey="Marcoval J" first="J." last="Marcoval">J. Marcoval</name>
<affiliation><mods:affiliation>Departments of Dermatology, Internal Medicine</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Ma A, J" sort="Ma A, J" uniqKey="Ma A J" first="J." last="Ma A">J. Ma A</name>
<affiliation><mods:affiliation>Departments of Dermatology, Internal Medicine</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Moreno, A" sort="Moreno, A" uniqKey="Moreno A" first="A." last="Moreno">A. Moreno</name>
<affiliation><mods:affiliation>Pathology, Hospital de Bellvitge, c/Feixa Llarga s/n, Hospitalet de Llobregat, University of Barcelona, 08907 Barcelona, Spain</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Peyri, J" sort="Peyri, J" uniqKey="Peyri J" first="J." last="Peyri">J. Peyri</name>
<affiliation><mods:affiliation>Departments of Dermatology, Internal Medicine</mods:affiliation>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j" type="main">British Journal of Dermatology</title>
<title level="j" type="alt">BRITISH JOURNAL OF DERMATOLOGY</title>
<idno type="ISSN">0007-0963</idno>
<idno type="eISSN">1365-2133</idno>
<imprint><biblScope unit="vol">153</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="790">790</biblScope>
<biblScope unit="page" to="794">794</biblScope>
<biblScope unit="page-count">5</biblScope>
<publisher>Blackwell Science Ltd</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="2005-10">2005-10</date>
</imprint>
<idno type="ISSN">0007-0963</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0007-0963</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Background Subcutaneous sarcoidosis is a specific cutaneous lesion of sarcoidosis that is rarely reported. Objective Our purpose was to analyse the clinicopathological features of 10 patients with subcutaneous sarcoidosis and its relationship with the systemic features of the disease. Patients and methods The patients with systemic sarcoidosis, diagnosed from 1974 to 2002 at a university hospital in Barcelona, Spain, who developed subcutaneous involvement, were included in the study. The diagnosis of systemic sarcoidosis was made according to conventional criteria. All the patients were monitored prospectively at the sarcoidosis clinic of the hospital. Skin biopsies were performed when granulomatous cutaneous involvement was suspected clinically. Results Granulomatous cutaneous involvement was demonstrated in 85 of 480 patients with systemic sarcoidosis. In 10 of these 85 patients subcutaneous sarcoidosis was diagnosed (11·8%). The lesions were most frequently located in the extremities, involving the forearms in nine patients. Indurated linear bands from the elbow to the hand were observed in five patients. In all of our patients the subcutaneous nodules appeared at the beginning of the disease. In six patients, the nodules remitted spontaneously in less than 2 years. In two cases foreign particles were detected under polarized light. Conclusions Subcutaneous sarcoidosis is a quite uniform clinicopathological entity usually appearing at the beginning of the disease. It usually heralds forms of sarcoidosis with nonsevere systemic involvement and is not associated with chronic fibrotic disease.</div>
</front>
</TEI>
<istex><corpusName>wiley</corpusName>
<keywords><teeft><json:string>sarcoidosis</json:string>
<json:string>subcutaneous</json:string>
<json:string>subcutaneous sarcoidosis</json:string>
<json:string>nodule</json:string>
<json:string>cutaneous</json:string>
<json:string>granulomatous</json:string>
<json:string>systemic sarcoidosis</json:string>
<json:string>lesion</json:string>
<json:string>granuloma</json:string>
<json:string>subcutaneous nodule</json:string>
<json:string>dermatol</json:string>
<json:string>marcoval</json:string>
<json:string>dermatology</json:string>
<json:string>corticosteroid</json:string>
<json:string>constitutional symptom</json:string>
<json:string>dermatologist</json:string>
<json:string>nodosum</json:string>
<json:string>erythema</json:string>
<json:string>foreign body</json:string>
<json:string>arch dermatol</json:string>
<json:string>linear band</json:string>
<json:string>erythema nodosum</json:string>
<json:string>british association</json:string>
<json:string>dermatologist british journal</json:string>
<json:string>indurated</json:string>
<json:string>clinicopathological</json:string>
<json:string>sarcoid</json:string>
<json:string>barcelona</json:string>
<json:string>systemic</json:string>
<json:string>indurated linear band</json:string>
<json:string>subcutaneous lesion</json:string>
<json:string>granulomatous cutaneous involvement</json:string>
<json:string>noncaseating granuloma</json:string>
<json:string>systemic involvement</json:string>
<json:string>specific cutaneous lesion</json:string>
<json:string>present study</json:string>
<json:string>systemic feature</json:string>
</teeft>
</keywords>
<author><json:item><name>J. Marcoval</name>
<affiliations><json:string>Departments of Dermatology, Internal Medicine</json:string>
</affiliations>
</json:item>
<json:item><name>J. Maña</name>
<affiliations><json:string>Departments of Dermatology, Internal Medicine</json:string>
</affiliations>
</json:item>
<json:item><name>A. Moreno</name>
<affiliations><json:string>Pathology, Hospital de Bellvitge, c/Feixa Llarga s/n, Hospitalet de Llobregat, University of Barcelona, 08907 Barcelona, Spain</json:string>
</affiliations>
</json:item>
<json:item><name>J. Peyri</name>
<affiliations><json:string>Departments of Dermatology, Internal Medicine</json:string>
</affiliations>
</json:item>
</author>
<subject><json:item><lang><json:string>eng</json:string>
</lang>
<value>sarcoidosis</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>skin</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>subcutaneous sarcoidosis</value>
</json:item>
</subject>
<articleId><json:string>BJD6815</json:string>
</articleId>
<arkIstex>ark:/67375/WNG-P9N0TSXN-V</arkIstex>
<language><json:string>eng</json:string>
</language>
<originalGenre><json:string>article</json:string>
</originalGenre>
<abstract>Background Subcutaneous sarcoidosis is a specific cutaneous lesion of sarcoidosis that is rarely reported. Objective Our purpose was to analyse the clinicopathological features of 10 patients with subcutaneous sarcoidosis and its relationship with the systemic features of the disease. Patients and methods The patients with systemic sarcoidosis, diagnosed from 1974 to 2002 at a university hospital in Barcelona, Spain, who developed subcutaneous involvement, were included in the study. The diagnosis of systemic sarcoidosis was made according to conventional criteria. All the patients were monitored prospectively at the sarcoidosis clinic of the hospital. Skin biopsies were performed when granulomatous cutaneous involvement was suspected clinically. Results Granulomatous cutaneous involvement was demonstrated in 85 of 480 patients with systemic sarcoidosis. In 10 of these 85 patients subcutaneous sarcoidosis was diagnosed (11·8%). The lesions were most frequently located in the extremities, involving the forearms in nine patients. Indurated linear bands from the elbow to the hand were observed in five patients. In all of our patients the subcutaneous nodules appeared at the beginning of the disease. In six patients, the nodules remitted spontaneously in less than 2 years. In two cases foreign particles were detected under polarized light. Conclusions Subcutaneous sarcoidosis is a quite uniform clinicopathological entity usually appearing at the beginning of the disease. It usually heralds forms of sarcoidosis with nonsevere systemic involvement and is not associated with chronic fibrotic disease.</abstract>
<qualityIndicators><score>6.953</score>
<pdfWordCount>2217</pdfWordCount>
<pdfCharCount>14277</pdfCharCount>
<pdfVersion>1.4</pdfVersion>
<pdfPageCount>5</pdfPageCount>
<pdfPageSize>595.307 x 782.307 pts</pdfPageSize>
<pdfWordsPerPage>443</pdfWordsPerPage>
<pdfText>true</pdfText>
<refBibsNative>true</refBibsNative>
<abstractWordCount>228</abstractWordCount>
<abstractCharCount>1625</abstractCharCount>
<keywordCount>3</keywordCount>
</qualityIndicators>
<title>Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
<pmid><json:string>16181462</json:string>
</pmid>
<genre><json:string>article</json:string>
</genre>
<host><title>British Journal of Dermatology</title>
<language><json:string>unknown</json:string>
</language>
<doi><json:string>10.1111/(ISSN)1365-2133</json:string>
</doi>
<issn><json:string>0007-0963</json:string>
</issn>
<eissn><json:string>1365-2133</json:string>
</eissn>
<publisherId><json:string>BJD</json:string>
</publisherId>
<volume>153</volume>
<issue>4</issue>
<pages><first>790</first>
<last>794</last>
<total>5</total>
</pages>
<genre><json:string>journal</json:string>
</genre>
</host>
<namedEntities><unitex><date><json:string>2005</json:string>
<json:string>1993</json:string>
</date>
<geogName></geogName>
<orgName><json:string>University Hospital of Bellvitge</json:string>
<json:string>Spain Summary Correspondence J Marcoval MD</json:string>
</orgName>
<orgName_funder></orgName_funder>
<orgName_provider></orgName_provider>
<persName><json:string>J. Mana</json:string>
<json:string>A. Moreno</json:string>
<json:string>J. Peyri</json:string>
</persName>
<placeName><json:string>Barcelona</json:string>
<json:string>Spain</json:string>
</placeName>
<ref_url></ref_url>
<ref_bibl><json:string>Kalb et al.</json:string>
<json:string>J. Marcoval et al.</json:string>
</ref_bibl>
<bibl></bibl>
</unitex>
</namedEntities>
<ark><json:string>ark:/67375/WNG-P9N0TSXN-V</json:string>
</ark>
<categories><wos><json:string>1 - science</json:string>
<json:string>2 - dermatology</json:string>
</wos>
<scienceMetrix><json:string>1 - health sciences</json:string>
<json:string>2 - clinical medicine</json:string>
<json:string>3 - dermatology & venereal diseases</json:string>
</scienceMetrix>
<scopus><json:string>1 - Health Sciences</json:string>
<json:string>2 - Medicine</json:string>
<json:string>3 - Dermatology</json:string>
</scopus>
<inist><json:string>1 - sciences appliquees, technologies et medecines</json:string>
<json:string>2 - sciences biologiques et medicales</json:string>
<json:string>3 - sciences medicales</json:string>
</inist>
</categories>
<publicationDate>2005</publicationDate>
<copyrightDate>2005</copyrightDate>
<doi><json:string>10.1111/j.1365-2133.2005.06815.x</json:string>
</doi>
<id>84FA235B9B5DBFBDFDBCBEAAF3C7091160D2ED7E</id>
<score>1</score>
<fulltext><json:item><extension>pdf</extension>
<original>true</original>
<mimetype>application/pdf</mimetype>
<uri>https://api.istex.fr/ark:/67375/WNG-P9N0TSXN-V/fulltext.pdf</uri>
</json:item>
<json:item><extension>zip</extension>
<original>false</original>
<mimetype>application/zip</mimetype>
<uri>https://api.istex.fr/ark:/67375/WNG-P9N0TSXN-V/bundle.zip</uri>
</json:item>
<istex:fulltextTEI uri="https://api.istex.fr/ark:/67375/WNG-P9N0TSXN-V/fulltext.tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main">Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
<title level="a" type="short">Subcutaneous sarcoidosis</title>
</titleStmt>
<publicationStmt><authority>ISTEX</authority>
<publisher>Blackwell Science Ltd</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="2005-10"></date>
</publicationStmt>
<notesStmt><note type="content-type" subtype="article" source="article" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</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="article"><analytic><title level="a" type="main">Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
<title level="a" type="short">Subcutaneous sarcoidosis</title>
<author xml:id="author-0000"><persName><forename type="first">J.</forename>
<surname>Marcoval</surname>
</persName>
<affiliation><orgName type="department">Departments of Dermatology</orgName>
<address><addrLine>Internal Medicine</addrLine>
</address>
</affiliation>
</author>
<author xml:id="author-0001"><persName><forename type="first">J.</forename>
<surname>Maña</surname>
</persName>
<affiliation><orgName type="department">Departments of Dermatology</orgName>
<address><addrLine>Internal Medicine</addrLine>
</address>
</affiliation>
</author>
<author xml:id="author-0002"><persName><forename type="first">A.</forename>
<surname>Moreno</surname>
</persName>
<affiliation><orgName type="department">Pathology</orgName>
<orgName type="institution">Hospital de Bellvitge</orgName>
<address><addrLine>c/Feixa Llarga s/n</addrLine>
<addrLine>Hospitalet de Llobregat, University of Barcelona, 08907 Barcelona, Spain</addrLine>
<country key="ES" xml:lang="en">SPAIN</country>
</address>
</affiliation>
</author>
<author xml:id="author-0003"><persName><forename type="first">J.</forename>
<surname>Peyri</surname>
</persName>
<affiliation><orgName type="department">Departments of Dermatology</orgName>
<address><addrLine>Internal Medicine</addrLine>
</address>
</affiliation>
</author>
<idno type="istex">84FA235B9B5DBFBDFDBCBEAAF3C7091160D2ED7E</idno>
<idno type="ark">ark:/67375/WNG-P9N0TSXN-V</idno>
<idno type="DOI">10.1111/j.1365-2133.2005.06815.x</idno>
<idno type="unit">BJD6815</idno>
<idno type="toTypesetVersion">file:BJD.BJD6815.pdf</idno>
</analytic>
<monogr><title level="j" type="main">British Journal of Dermatology</title>
<title level="j" type="alt">BRITISH JOURNAL OF DERMATOLOGY</title>
<idno type="pISSN">0007-0963</idno>
<idno type="eISSN">1365-2133</idno>
<idno type="book-DOI">10.1111/(ISSN)1365-2133</idno>
<idno type="book-part-DOI">10.1111/bjd.2005.153.issue-4</idno>
<idno type="product">BJD</idno>
<idno type="publisherDivision">ST</idno>
<imprint><biblScope unit="vol">153</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="790">790</biblScope>
<biblScope unit="page" to="794">794</biblScope>
<biblScope unit="page-count">5</biblScope>
<publisher>Blackwell Science Ltd</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="2005-10"></date>
</imprint>
</monogr>
</biblStruct>
</sourceDesc>
</fileDesc>
<encodingDesc><schemaRef type="ODD" url="https://xml-schema.delivery.istex.fr/tei-istex.odd"></schemaRef>
<appInfo><application ident="pub2tei" version="1.0.10" when="2019-12-20"><label>pub2TEI-ISTEX</label>
<desc>A set of style sheets for converting XML documents encoded in various scientific publisher formats into a common TEI format.
<ref target="http://www.tei-c.org/">We use TEI</ref>
</desc>
</application>
</appInfo>
</encodingDesc>
<profileDesc><abstract xml:lang="en" style="main"><head>Summary</head>
<p><hi rend="bold">Background </hi>
Subcutaneous sarcoidosis is a specific cutaneous lesion of sarcoidosis that is rarely reported.</p>
<p><hi rend="bold">Objective </hi>
Our purpose was to analyse the clinicopathological features of 10 patients with subcutaneous sarcoidosis and its relationship with the systemic features of the disease.</p>
<p><hi rend="bold">Patients and methods </hi>
The patients with systemic sarcoidosis, diagnosed from 1974 to 2002 at a university hospital in Barcelona, Spain, who developed subcutaneous involvement, were included in the study. The diagnosis of systemic sarcoidosis was made according to conventional criteria. All the patients were monitored prospectively at the sarcoidosis clinic of the hospital. Skin biopsies were performed when granulomatous cutaneous involvement was suspected clinically.</p>
<p><hi rend="bold">Results </hi>
Granulomatous cutaneous involvement was demonstrated in 85 of 480 patients with systemic sarcoidosis. In 10 of these 85 patients subcutaneous sarcoidosis was diagnosed (11·8%). The lesions were most frequently located in the extremities, involving the forearms in nine patients. Indurated linear bands from the elbow to the hand were observed in five patients. In all of our patients the subcutaneous nodules appeared at the beginning of the disease. In six patients, the nodules remitted spontaneously in less than 2 years. In two cases foreign particles were detected under polarized light.</p>
<p><hi rend="bold">Conclusions </hi>
Subcutaneous sarcoidosis is a quite uniform clinicopathological entity usually appearing at the beginning of the disease. It usually heralds forms of sarcoidosis with nonsevere systemic involvement and is not associated with chronic fibrotic disease.</p>
</abstract>
<textClass><keywords xml:lang="en"><term xml:id="k1">sarcoidosis</term>
<term xml:id="k2">skin</term>
<term xml:id="k3">subcutaneous sarcoidosis</term>
</keywords>
<keywords rend="tocHeading1"><term>Dermatopathology</term>
</keywords>
</textClass>
<langUsage><language ident="en"></language>
</langUsage>
</profileDesc>
<revisionDesc><change when="2019-12-20" who="#istex" xml:id="pub2tei">formatting</change>
</revisionDesc>
</teiHeader>
</istex:fulltextTEI>
<json:item><extension>txt</extension>
<original>false</original>
<mimetype>text/plain</mimetype>
<uri>https://api.istex.fr/ark:/67375/WNG-P9N0TSXN-V/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)1365-2133</doi>
<issn type="print">0007-0963</issn>
<issn type="electronic">1365-2133</issn>
<idGroup><id type="product" value="BJD"></id>
<id type="publisherDivision" value="ST"></id>
</idGroup>
<titleGroup><title type="main" sort="BRITISH JOURNAL OF DERMATOLOGY">British Journal of Dermatology</title>
</titleGroup>
</publicationMeta>
<publicationMeta level="part" position="10004"><doi origin="wiley">10.1111/bjd.2005.153.issue-4</doi>
<numberingGroup><numbering type="journalVolume" number="153">153</numbering>
<numbering type="journalIssue" number="4">4</numbering>
</numberingGroup>
<coverDate startDate="2005-10">October 2005</coverDate>
</publicationMeta>
<publicationMeta level="unit" type="article" position="15" status="forIssue"><doi origin="wiley">10.1111/j.1365-2133.2005.06815.x</doi>
<idGroup><id type="unit" value="BJD6815"></id>
</idGroup>
<countGroup><count type="pageTotal" number="5"></count>
</countGroup>
<titleGroup><title type="tocHeading1">Dermatopathology</title>
</titleGroup>
<eventGroup><event type="firstOnline" date="2005-08-11"></event>
<event type="publishedOnlineFinalForm" date="2005-09-16"></event>
<event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.9 mode:FullText source:FullText result:FullText" date="2010-06-24"></event>
<event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:4.0.1" date="2014-03-15"></event>
<event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-15"></event>
</eventGroup>
<numberingGroup><numbering type="pageFirst" number="790">790</numbering>
<numbering type="pageLast" number="794">794</numbering>
</numberingGroup>
<correspondenceTo>J Marcoval MD.
E‐mail: <email>jmarcoval@csub.scs.es</email>
</correspondenceTo>
<linkGroup><link type="toTypesetVersion" href="file:BJD.BJD6815.pdf"></link>
</linkGroup>
</publicationMeta>
<contentMeta><unparsedEditorialHistory>Accepted for publication 22 February 2005</unparsedEditorialHistory>
<countGroup><count type="figureTotal" number="2"></count>
<count type="tableTotal" number="1"></count>
<count type="formulaTotal" number="0"></count>
<count type="referenceTotal" number="16"></count>
<count type="wordTotal" number="2079"></count>
<count type="linksPubMed" number="0"></count>
<count type="linksCrossRef" number="0"></count>
</countGroup>
<titleGroup><title type="main">Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
<title type="shortAuthors">J. Marcoval <i>et al.</i>
</title>
<title type="short">Subcutaneous sarcoidosis</title>
</titleGroup>
<creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>J.</givenNames>
<familyName>Marcoval</familyName>
</personName>
</creator>
<creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>J.</givenNames>
<familyName>Maña</familyName>
</personName>
</creator>
<creator creatorRole="author" xml:id="cr3" affiliationRef="#a2"><personName><givenNames>A.</givenNames>
<familyName>Moreno</familyName>
</personName>
</creator>
<creator creatorRole="author" xml:id="cr4" affiliationRef="#a1"><personName><givenNames>J.</givenNames>
<familyName>Peyri</familyName>
</personName>
</creator>
</creators>
<affiliationGroup><affiliation xml:id="a1"><unparsedAffiliation>Departments of Dermatology, Internal Medicine</unparsedAffiliation>
</affiliation>
<affiliation xml:id="a2" countryCode="ES"><unparsedAffiliation>Pathology, Hospital de Bellvitge, c/Feixa Llarga s/n, Hospitalet de Llobregat, University of Barcelona, 08907 Barcelona, Spain</unparsedAffiliation>
</affiliation>
</affiliationGroup>
<keywordGroup xml:lang="en"><keyword xml:id="k1">sarcoidosis</keyword>
<keyword xml:id="k2">skin</keyword>
<keyword xml:id="k3">subcutaneous sarcoidosis</keyword>
</keywordGroup>
<abstractGroup><abstract type="main" xml:lang="en"><title type="main">Summary</title>
<p><b>Background </b>
Subcutaneous sarcoidosis is a specific cutaneous lesion of sarcoidosis that is rarely reported.</p>
<p><b>Objective </b>
Our purpose was to analyse the clinicopathological features of 10 patients with subcutaneous sarcoidosis and its relationship with the systemic features of the disease.</p>
<p><b>Patients and methods </b>
The patients with systemic sarcoidosis, diagnosed from 1974 to 2002 at a university hospital in Barcelona, Spain, who developed subcutaneous involvement, were included in the study. The diagnosis of systemic sarcoidosis was made according to conventional criteria. All the patients were monitored prospectively at the sarcoidosis clinic of the hospital. Skin biopsies were performed when granulomatous cutaneous involvement was suspected clinically.</p>
<p><b>Results </b>
Granulomatous cutaneous involvement was demonstrated in 85 of 480 patients with systemic sarcoidosis. In 10 of these 85 patients subcutaneous sarcoidosis was diagnosed (11·8%). The lesions were most frequently located in the extremities, involving the forearms in nine patients. Indurated linear bands from the elbow to the hand were observed in five patients. In all of our patients the subcutaneous nodules appeared at the beginning of the disease. In six patients, the nodules remitted spontaneously in less than 2 years. In two cases foreign particles were detected under polarized light.</p>
<p><b>Conclusions </b>
Subcutaneous sarcoidosis is a quite uniform clinicopathological entity usually appearing at the beginning of the disease. It usually heralds forms of sarcoidosis with nonsevere systemic involvement and is not associated with chronic fibrotic disease.</p>
</abstract>
</abstractGroup>
</contentMeta>
<noteGroup><note xml:id="fn1" numbered="no"><p>Conflicts of interest: None declared.</p>
</note>
</noteGroup>
</header>
</component>
</istex:document>
</istex:metadataXml>
<mods version="3.6"><titleInfo lang="en"><title>Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
</titleInfo>
<titleInfo type="abbreviated" lang="en"><title>Subcutaneous sarcoidosis</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en"><title>Subcutaneous sarcoidosis—clinicopathological study of 10 cases</title>
</titleInfo>
<name type="personal"><namePart type="given">J.</namePart>
<namePart type="family">Marcoval</namePart>
<affiliation>Departments of Dermatology, Internal Medicine</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">J.</namePart>
<namePart type="family">Maña</namePart>
<affiliation>Departments of Dermatology, Internal Medicine</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">A.</namePart>
<namePart type="family">Moreno</namePart>
<affiliation>Pathology, Hospital de Bellvitge, c/Feixa Llarga s/n, Hospitalet de Llobregat, University of Barcelona, 08907 Barcelona, Spain</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">J.</namePart>
<namePart type="family">Peyri</namePart>
<affiliation>Departments of Dermatology, Internal Medicine</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<typeOfResource>text</typeOfResource>
<genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre>
<originInfo><publisher>Blackwell Science Ltd</publisher>
<place><placeTerm type="text">Oxford, UK</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2005-10</dateIssued>
<edition>Accepted for publication 22 February 2005</edition>
<copyrightDate encoding="w3cdtf">2005</copyrightDate>
</originInfo>
<language><languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
</language>
<physicalDescription><extent unit="figures">2</extent>
<extent unit="tables">1</extent>
<extent unit="formulas">0</extent>
<extent unit="references">16</extent>
<extent unit="linksCrossRef">0</extent>
<extent unit="words">2079</extent>
</physicalDescription>
<abstract lang="en">Background Subcutaneous sarcoidosis is a specific cutaneous lesion of sarcoidosis that is rarely reported. Objective Our purpose was to analyse the clinicopathological features of 10 patients with subcutaneous sarcoidosis and its relationship with the systemic features of the disease. Patients and methods The patients with systemic sarcoidosis, diagnosed from 1974 to 2002 at a university hospital in Barcelona, Spain, who developed subcutaneous involvement, were included in the study. The diagnosis of systemic sarcoidosis was made according to conventional criteria. All the patients were monitored prospectively at the sarcoidosis clinic of the hospital. Skin biopsies were performed when granulomatous cutaneous involvement was suspected clinically. Results Granulomatous cutaneous involvement was demonstrated in 85 of 480 patients with systemic sarcoidosis. In 10 of these 85 patients subcutaneous sarcoidosis was diagnosed (11·8%). The lesions were most frequently located in the extremities, involving the forearms in nine patients. Indurated linear bands from the elbow to the hand were observed in five patients. In all of our patients the subcutaneous nodules appeared at the beginning of the disease. In six patients, the nodules remitted spontaneously in less than 2 years. In two cases foreign particles were detected under polarized light. Conclusions Subcutaneous sarcoidosis is a quite uniform clinicopathological entity usually appearing at the beginning of the disease. It usually heralds forms of sarcoidosis with nonsevere systemic involvement and is not associated with chronic fibrotic disease.</abstract>
<subject lang="en"><genre>keywords</genre>
<topic>sarcoidosis</topic>
<topic>skin</topic>
<topic>subcutaneous sarcoidosis</topic>
</subject>
<relatedItem type="host"><titleInfo><title>British Journal of Dermatology</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">0007-0963</identifier>
<identifier type="eISSN">1365-2133</identifier>
<identifier type="DOI">10.1111/(ISSN)1365-2133</identifier>
<identifier type="PublisherID">BJD</identifier>
<part><date>2005</date>
<detail type="volume"><caption>vol.</caption>
<number>153</number>
</detail>
<detail type="issue"><caption>no.</caption>
<number>4</number>
</detail>
<extent unit="pages"><start>790</start>
<end>794</end>
<total>5</total>
</extent>
</part>
</relatedItem>
<relatedItem type="references" displayLabel="cit1"><titleInfo><title>ATS/ERS/WASOG statement on sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">GW</namePart>
<namePart type="family">Hunninghake</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">U</namePart>
<namePart type="family">Costabel</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">M</namePart>
<namePart type="family">Ando</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Hunninghake GW, Costabel U, Ando M et al. ATS/ERS/WASOG statement on sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis 1999; 16: 149–73.</note>
<part><date>1999</date>
<detail type="volume"><caption>vol.</caption>
<number>16</number>
</detail>
<extent unit="pages"><start>149</start>
<end>73</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Sarcoidosis Vasc Diffuse Lung Dis</title>
</titleInfo>
<part><date>1999</date>
<detail type="volume"><caption>vol.</caption>
<number>16</number>
</detail>
<extent unit="pages"><start>149</start>
<end>73</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit2"><titleInfo><title>Cutaneous involvement in sarcoidosis. Relationship to systemic disease</title>
</titleInfo>
<name type="personal"><namePart type="given">J</namePart>
<namePart type="family">Mañá</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">J</namePart>
<namePart type="family">Marcoval</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">J</namePart>
<namePart type="family">Graells</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Mañá J, Marcoval J, Graells J et al. Cutaneous involvement in sarcoidosis. Relationship to systemic disease. Arch Dermatol 1997; 133: 882–8.</note>
<part><date>1997</date>
<detail type="volume"><caption>vol.</caption>
<number>133</number>
</detail>
<extent unit="pages"><start>882</start>
<end>8</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Arch Dermatol</title>
</titleInfo>
<part><date>1997</date>
<detail type="volume"><caption>vol.</caption>
<number>133</number>
</detail>
<extent unit="pages"><start>882</start>
<end>8</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit3"><titleInfo><title>Dermatological aspects of sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">DG</namePart>
<namePart type="family">James</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">James DG. Dermatological aspects of sarcoidosis. Quart J Med 1959; 28: 109–24.</note>
<part><date>1959</date>
<detail type="volume"><caption>vol.</caption>
<number>28</number>
</detail>
<extent unit="pages"><start>109</start>
<end>24</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Quart J Med</title>
</titleInfo>
<part><date>1959</date>
<detail type="volume"><caption>vol.</caption>
<number>28</number>
</detail>
<extent unit="pages"><start>109</start>
<end>24</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit4"><titleInfo><title>Sarcoidosis of the skin</title>
</titleInfo>
<name type="personal"><namePart type="given">JG</namePart>
<namePart type="family">Scadding</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">DN</namePart>
<namePart type="family">Mitchell</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>book-chapter</genre>
<relatedItem type="host"><titleInfo><title>Sarcoidosis</title>
</titleInfo>
<originInfo><publisher>Chapman & Hall Medical</publisher>
</originInfo>
<part><date>1985</date>
<extent unit="pages"><start>181</start>
<end>206</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit5"><titleInfo><title>Cutaneous sarcoidosis: definitions and types of lesions</title>
</titleInfo>
<name type="personal"><namePart type="given">ML</namePart>
<namePart type="family">Elgart</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Elgart ML. Cutaneous sarcoidosis: definitions and types of lesions. Clin Dermatol 1986; 4: 35–45.</note>
<part><date>1986</date>
<detail type="volume"><caption>vol.</caption>
<number>4</number>
</detail>
<extent unit="pages"><start>35</start>
<end>45</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Clin Dermatol</title>
</titleInfo>
<part><date>1986</date>
<detail type="volume"><caption>vol.</caption>
<number>4</number>
</detail>
<extent unit="pages"><start>35</start>
<end>45</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit6"><titleInfo><title>Sarcoidosis with subcutaneous nodules</title>
</titleInfo>
<name type="personal"><namePart type="given">RF</namePart>
<namePart type="family">Kalb</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">W</namePart>
<namePart type="family">Epstein</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">ME</namePart>
<namePart type="family">Grossman</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Kalb RF, Epstein W, Grossman ME. Sarcoidosis with subcutaneous nodules. Am J Med 1988; 85: 731–6.</note>
<part><date>1988</date>
<detail type="volume"><caption>vol.</caption>
<number>85</number>
</detail>
<extent unit="pages"><start>731</start>
<end>6</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Am J Med</title>
</titleInfo>
<part><date>1988</date>
<detail type="volume"><caption>vol.</caption>
<number>85</number>
</detail>
<extent unit="pages"><start>731</start>
<end>6</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit7"><titleInfo><title>Manifestations of sarcoidosis: analysis of 145 patients with a review of nine series selected from the literature</title>
</titleInfo>
<name type="personal"><namePart type="given">RL</namePart>
<namePart type="family">Mayock</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">P</namePart>
<namePart type="family">Bertrand</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">CE</namePart>
<namePart type="family">Morrison</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">JH</namePart>
<namePart type="family">Scott</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Mayock RL, Bertrand P, Morrison CE, Scott JH. Manifestations of sarcoidosis: analysis of 145 patients with a review of nine series selected from the literature. Am J Med 1963; 35: 67–89.</note>
<part><date>1963</date>
<detail type="volume"><caption>vol.</caption>
<number>35</number>
</detail>
<extent unit="pages"><start>67</start>
<end>89</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Am J Med</title>
</titleInfo>
<part><date>1963</date>
<detail type="volume"><caption>vol.</caption>
<number>35</number>
</detail>
<extent unit="pages"><start>67</start>
<end>89</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit8"><titleInfo><title>Subcutaneous sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">D</namePart>
<namePart type="family">Vainsencher</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">RK</namePart>
<namePart type="family">Winkelmann</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Vainsencher D, Winkelmann RK. Subcutaneous sarcoidosis. Arch Dermatol 1984; 120: 1028–31.</note>
<part><date>1984</date>
<detail type="volume"><caption>vol.</caption>
<number>120</number>
</detail>
<extent unit="pages"><start>1028</start>
<end>31</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Arch Dermatol</title>
</titleInfo>
<part><date>1984</date>
<detail type="volume"><caption>vol.</caption>
<number>120</number>
</detail>
<extent unit="pages"><start>1028</start>
<end>31</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit9"><titleInfo><title>Subcutaneous sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">EM</namePart>
<namePart type="family">Higgins</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">JR</namePart>
<namePart type="family">Salisbury</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">AWP</namePart>
<namePart type="family">Du Vivier</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Higgins EM, Salisbury JR, Du Vivier AWP. Subcutaneous sarcoidosis. Clin Exp Dermatol 1993; 18: 65–6.</note>
<part><date>1993</date>
<detail type="volume"><caption>vol.</caption>
<number>18</number>
</detail>
<extent unit="pages"><start>65</start>
<end>6</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Clin Exp Dermatol</title>
</titleInfo>
<part><date>1993</date>
<detail type="volume"><caption>vol.</caption>
<number>18</number>
</detail>
<extent unit="pages"><start>65</start>
<end>6</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit10"><titleInfo><title>Subcutaneous sarcoidosis with dactylitis</title>
</titleInfo>
<name type="personal"><namePart type="given">N</namePart>
<namePart type="family">Curcó</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">X</namePart>
<namePart type="family">Pagerols</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">P</namePart>
<namePart type="family">Vives</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Curcó N, Pagerols X, Vives P. Subcutaneous sarcoidosis with dactylitis. Clin Exp Dermatol 1995; 20: 434–5.</note>
<part><date>1995</date>
<detail type="volume"><caption>vol.</caption>
<number>20</number>
</detail>
<extent unit="pages"><start>434</start>
<end>5</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Clin Exp Dermatol</title>
</titleInfo>
<part><date>1995</date>
<detail type="volume"><caption>vol.</caption>
<number>20</number>
</detail>
<extent unit="pages"><start>434</start>
<end>5</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit11"><titleInfo><title>Coexistence of subcutaneous sarcoidosis and scar sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">T</namePart>
<namePart type="family">Ohi</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">S</namePart>
<namePart type="family">Saijo</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">H</namePart>
<namePart type="family">Tagami</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Ohi T, Saijo S, Tagami H. Coexistence of subcutaneous sarcoidosis and scar sarcoidosis. Acta Derm Venereol 1996; 76: 500.</note>
<part><date>1996</date>
<detail type="volume"><caption>vol.</caption>
<number>76</number>
</detail>
<extent unit="pages"><start>500</start>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Acta Derm Venereol</title>
</titleInfo>
<part><date>1996</date>
<detail type="volume"><caption>vol.</caption>
<number>76</number>
</detail>
<extent unit="pages"><start>500</start>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit12"><titleInfo><title>The natural history of the sarcoid granuloma</title>
</titleInfo>
<name type="personal"><namePart type="given">HJ</namePart>
<namePart type="family">Barrier</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">A</namePart>
<namePart type="family">Bogoch</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Barrier HJ, Bogoch A. The natural history of the sarcoid granuloma. Am J Pathol 1953; 29: 451–69.</note>
<part><date>1953</date>
<detail type="volume"><caption>vol.</caption>
<number>29</number>
</detail>
<extent unit="pages"><start>451</start>
<end>69</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Am J Pathol</title>
</titleInfo>
<part><date>1953</date>
<detail type="volume"><caption>vol.</caption>
<number>29</number>
</detail>
<extent unit="pages"><start>451</start>
<end>69</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit13"><titleInfo><title>Foreign bodies in granulomatous cutaneous lesions of patients with systemic sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">J</namePart>
<namePart type="family">Marcoval</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">J</namePart>
<namePart type="family">Mañá</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">A</namePart>
<namePart type="family">Moreno</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Marcoval J, Mañá J, Moreno A et al. Foreign bodies in granulomatous cutaneous lesions of patients with systemic sarcoidosis. Arch Dermatol 2001; 137: 427–30.</note>
<part><date>2001</date>
<detail type="volume"><caption>vol.</caption>
<number>137</number>
</detail>
<extent unit="pages"><start>427</start>
<end>30</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Arch Dermatol</title>
</titleInfo>
<part><date>2001</date>
<detail type="volume"><caption>vol.</caption>
<number>137</number>
</detail>
<extent unit="pages"><start>427</start>
<end>30</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit14"><titleInfo><title>Foreign bodies in sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">YC</namePart>
<namePart type="family">Kim</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">MK</namePart>
<namePart type="family">Triffet</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">LE</namePart>
<namePart type="family">Gibson</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Kim YC, Triffet MK, Gibson LE. Foreign bodies in sarcoidosis. Am J Dermatopathol 2000; 22: 408–12.</note>
<part><date>2000</date>
<detail type="volume"><caption>vol.</caption>
<number>22</number>
</detail>
<extent unit="pages"><start>408</start>
<end>12</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Am J Dermatopathol</title>
</titleInfo>
<part><date>2000</date>
<detail type="volume"><caption>vol.</caption>
<number>22</number>
</detail>
<extent unit="pages"><start>408</start>
<end>12</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit15"><titleInfo><title>The presence of foreign bodies does not exclude the diagnosis of sarcoidosis</title>
</titleInfo>
<name type="personal"><namePart type="given">JP</namePart>
<namePart type="family">Callen</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Callen JP. The presence of foreign bodies does not exclude the diagnosis of sarcoidosis. Arch Dermatol 2001; 137: 485–6.</note>
<part><date>2001</date>
<detail type="volume"><caption>vol.</caption>
<number>137</number>
</detail>
<extent unit="pages"><start>485</start>
<end>6</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Arch Dermatol</title>
</titleInfo>
<part><date>2001</date>
<detail type="volume"><caption>vol.</caption>
<number>137</number>
</detail>
<extent unit="pages"><start>485</start>
<end>6</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<relatedItem type="references" displayLabel="cit16"><titleInfo><title>Subcutaneous nodules in a patient with hydrocephalus</title>
</titleInfo>
<name type="personal"><namePart type="given">JK</namePart>
<namePart type="family">Chiang</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">LC</namePart>
<namePart type="family">Ortiz‐Ferrer</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">K</namePart>
<namePart type="family">Remlinger</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">DM</namePart>
<namePart type="family">Bronson</namePart>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<genre>journal-article</genre>
<note type="citation/reference">Chiang JK, Ortiz‐Ferrer LC, Remlinger K, Bronson DM. Subcutaneous nodules in a patient with hydrocephalus. Arch Dermatol 2002; 138: 259–64.</note>
<part><date>2002</date>
<detail type="volume"><caption>vol.</caption>
<number>138</number>
</detail>
<extent unit="pages"><start>259</start>
<end>64</end>
</extent>
</part>
<relatedItem type="host"><titleInfo><title>Arch Dermatol</title>
</titleInfo>
<part><date>2002</date>
<detail type="volume"><caption>vol.</caption>
<number>138</number>
</detail>
<extent unit="pages"><start>259</start>
<end>64</end>
</extent>
</part>
</relatedItem>
</relatedItem>
<identifier type="istex">84FA235B9B5DBFBDFDBCBEAAF3C7091160D2ED7E</identifier>
<identifier type="ark">ark:/67375/WNG-P9N0TSXN-V</identifier>
<identifier type="DOI">10.1111/j.1365-2133.2005.06815.x</identifier>
<identifier type="ArticleID">BJD6815</identifier>
<accessCondition type="use and reproduction" contentType="copyright">© Wiley. All rights reserved.</accessCondition>
<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>Converted from (version ) to MODS version 3.6.</recordOrigin>
<recordCreationDate encoding="w3cdtf">2019-11-13</recordCreationDate>
</recordInfo>
</mods>
<json:item><extension>json</extension>
<original>false</original>
<mimetype>application/json</mimetype>
<uri>https://api.istex.fr/ark:/67375/WNG-P9N0TSXN-V/record.json</uri>
</json:item>
</metadata>
<serie></serie>
</istex>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002366 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 002366 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= ChloroquineV1 |flux= Istex |étape= Corpus |type= RBID |clé= ISTEX:84FA235B9B5DBFBDFDBCBEAAF3C7091160D2ED7E |texte= Subcutaneous sarcoidosis—clinicopathological study of 10 cases }}
![]() | This area was generated with Dilib version V0.6.33. | ![]() |