Interstitial granulomatous dermatitis: a misdiagnosed cutaneous form of systemic lupus erythematosus?
Identifieur interne : 002236 ( Istex/Corpus ); précédent : 002235; suivant : 002237Interstitial granulomatous dermatitis: a misdiagnosed cutaneous form of systemic lupus erythematosus?
Auteurs : S. Blaise ; D. Salameire ; P. H. CarpentierSource :
- Clinical and Experimental Dermatology [ 0307-6938 ] ; 2008-11.
English descriptors
- Teeft :
- Acad, Acad dermatol, Adverse event, Aetiology, Antiphospholipid, Antiphospholipid syndrome, Atypical, Autoimmune, Autoimmune diseases, Blaise, British association, Clinical presentation, Cutaneous, Cutaneous lesions, Dermatitis, Dermatol, Dermatology, Erythematous, Experimental dermatology, Focal collagen necrosis, Granulomatous, Granulomatous dermatitis, Grenoble, Grenoble university hospital, Histological, Histological features, Immunological features, Interstitial, Interstitial granulomatous dermatitis, Journal compilation, Lupus, Macular eruption, Misdiagnosed, Misdiagnosed cutaneous form, Neutrophilic, Palisaded, Palisaded histiocytic granuloma, Palisaded neutrophilic, Primary antiphospholipid syndrome, Reticular, Rheumatoid, Rheumatoid factor, Systemic lupus erythematosus, Vascular medicine, Violaceous centre.
Abstract
Interstitial granulomatous dermatitis (IGD) is a recently described, rare dermatological entity. The clinical features are diverse and the precise aetiology is unknown. We present a rare and atypical case of IGD in a patient with systemic lupus erythematosus (SLE). A 26‐year‐old woman had been diagnosed with SLE when she was 15 years old. The diagnosis was based on cutaneous, articular, pulmonary, haematological and immunological features. The patient presented with a cutaneous diffuse macular eruption on the limbs, appearing in a cockade (rosette) pattern with a violaceous centre and erythematous surround. The face and trunk were spared. The cutaneous histological features led us to consider a diagnosis of IGD. The lesions disappeared after 15 days of systemic steroid therapy. This case is a new clinical form of IGD with an atypical location and clinical presentation. IGD has usually been associated with drug‐related adverse reactions and autoimmune diseases. Reports in the literature of IGD in patients with SLE are rare.
Url:
DOI: 10.1111/j.1365-2230.2008.02774.x
Links to Exploration step
ISTEX:B69BB28B046EBCDBD2F679BF23D72F9AD99B6DF6Le document en format XML
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H.</forename><surname>Carpentier</surname></persName><affiliation><orgName type="division">Department of Vascular Medicine</orgName></affiliation></author><idno type="istex">B69BB28B046EBCDBD2F679BF23D72F9AD99B6DF6</idno><idno type="ark">ark:/67375/WNG-S1HG82T2-4</idno><idno type="DOI">10.1111/j.1365-2230.2008.02774.x</idno><idno type="unit">CED2774</idno><idno type="toTypesetVersion">file:CED.CED2774.pdf</idno></analytic><monogr><title level="j" type="main">Clinical and Experimental Dermatology</title><title level="j" type="alt">CLINICAL EXPERIMENTAL DERMATOLOGY</title><idno type="pISSN">0307-6938</idno><idno type="eISSN">1365-2230</idno><idno type="book-DOI">10.1111/(ISSN)1365-2230</idno><idno type="book-part-DOI">10.1111/ced.2008.33.issue-6</idno><idno type="product">CED</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">33</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="712">712</biblScope><biblScope unit="page" to="714">714</biblScope><biblScope unit="page-count">3</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2008-11"></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.
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E‐mail: <email normalForm="sblaise@chu-grenoble.fr">sblaise@chu‐grenoble.fr</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CED.CED2774.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Accepted for publication 1 December 2007</unparsedEditorialHistory><countGroup><count type="figureTotal" number="3"></count><count type="tableTotal" number="0"></count></countGroup><titleGroup><title type="main">Interstitial granulomatous dermatitis: a misdiagnosed cutaneous form of systemic lupus erythematosus?</title><title type="shortAuthors"><i>S. Blaise</i> et al.</title><title type="short">Interstitial granulomatous dermatitis: a misdiagnosed cutaneous form of SLE?</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>S.</givenNames><familyName>Blaise</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a2"><personName><givenNames>D.</givenNames><familyName>Salameire</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a1"><personName><givenNames>P. H.</givenNames><familyName>Carpentier</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1"><unparsedAffiliation>Department of Vascular Medicine</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="FR"><unparsedAffiliation>Laboratory of Anatomopathology, Grenoble University Hospital, Grenoble, France</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Summary</title><p>Interstitial granulomatous dermatitis (IGD) is a recently described, rare dermatological entity. The clinical features are diverse and the precise aetiology is unknown. We present a rare and atypical case of IGD in a patient with systemic lupus erythematosus (SLE). A 26‐year‐old woman had been diagnosed with SLE when she was 15 years old. The diagnosis was based on cutaneous, articular, pulmonary, haematological and immunological features. The patient presented with a cutaneous diffuse macular eruption on the limbs, appearing in a cockade (rosette) pattern with a violaceous centre and erythematous surround. The face and trunk were spared. The cutaneous histological features led us to consider a diagnosis of IGD. The lesions disappeared after 15 days of systemic steroid therapy. This case is a new clinical form of IGD with an atypical location and clinical presentation. IGD has usually been associated with drug‐related adverse reactions and autoimmune diseases. Reports in the literature of IGD in patients with SLE are rare.</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn1" numbered="no"><p>Conflict of interest: none declared.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Interstitial granulomatous dermatitis: a misdiagnosed cutaneous form of systemic lupus erythematosus?</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Interstitial granulomatous dermatitis: a misdiagnosed cutaneous form of SLE?</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Interstitial granulomatous dermatitis: a misdiagnosed cutaneous form of systemic lupus erythematosus?</title></titleInfo><name type="personal"><namePart type="given">S.</namePart><namePart type="family">Blaise</namePart><affiliation>Department of Vascular Medicine</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D.</namePart><namePart type="family">Salameire</namePart><affiliation>Laboratory of Anatomopathology, Grenoble University Hospital, Grenoble, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">P. H.</namePart><namePart type="family">Carpentier</namePart><affiliation>Department of Vascular Medicine</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="brief-communication" displayLabel="shortCommunication" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-S9SX2MFS-0">brief-communication</genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2008-11</dateIssued><edition>Accepted for publication 1 December 2007</edition><copyrightDate encoding="w3cdtf">2008</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></physicalDescription><abstract lang="en">Interstitial granulomatous dermatitis (IGD) is a recently described, rare dermatological entity. The clinical features are diverse and the precise aetiology is unknown. We present a rare and atypical case of IGD in a patient with systemic lupus erythematosus (SLE). A 26‐year‐old woman had been diagnosed with SLE when she was 15 years old. The diagnosis was based on cutaneous, articular, pulmonary, haematological and immunological features. The patient presented with a cutaneous diffuse macular eruption on the limbs, appearing in a cockade (rosette) pattern with a violaceous centre and erythematous surround. The face and trunk were spared. The cutaneous histological features led us to consider a diagnosis of IGD. The lesions disappeared after 15 days of systemic steroid therapy. This case is a new clinical form of IGD with an atypical location and clinical presentation. IGD has usually been associated with drug‐related adverse reactions and autoimmune diseases. 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