Reticular erythematous mucinosis and thrombocytopenic purpura
Identifieur interne : 000370 ( Istex/Corpus ); précédent : 000369; suivant : 000371Reticular erythematous mucinosis and thrombocytopenic purpura
Auteurs : Suzanne W. Braddock ; Catharine S. Davis ; Richard B. DavisSource :
- Journal of the American Academy of Dermatology [ 0190-9622 ] ; 1988.
English descriptors
- Teeft :
- Abdomen chest, Alcian, American academy, Antimalarial drugs, Arch dermatol, Braddock, Chest chest, Cutaneous, Dermal, Dermatol, Dermis, Discoid lupus erythematosus, Electron microscopy, Eruption, Erythematous, Fibroblast, Hautkr, Hyperthyroidism, Idiopathic, Idiopathic thrombocytopenic purpura, Immune, Immune complexes, Immune function, Mucin, Mucinosis, Other diseases, Photosensitivity, Plaquelike, Plaquelike cutaneous mucinosis, Platelet, Pruritus, Purpura, Rash, Reticular, Reticular erythematous mucinosis, Reticular erythematous mucinosis syndrome, Solar sensitivity, Solar simulator, Steigleder, Syndrome, Thrombocytopenic, Thrombocytopenic purpura, Viral, World literature.
Abstract
A case of reticular erythematous mucinosis associated with chronic idiopathic thrombocytopenic purpura and circulating immune complexes is described. We compare reticular erythematous mucinosis with the similar plaquelike cutaneous mucinosis. We discuss the apparent photosensitivity of reticular erythematous mucinosis and its possible relationship with altered states of immune function such as diabetes, thyroid disease, and neoplasia. The somewhat varied but characteristic histopathologic findings and staining are reviewed, including the characteristic perivascular and occasional perifollicular lymphocytic infiltrate and Alcian blue-positive dermal mucin. Treatment with antimalarial drugs still appears to be the most uniformly successful therapeutic approach to the management of this chronic dermatosis. Further research efforts should be directed at understanding its link with altered states of immune function.
Url:
DOI: 10.1016/S0190-9622(88)70246-7
Links to Exploration step
ISTEX:DA2BB316F69C20EB9E106EA3640EB7DEE2F279DFLe document en format XML
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Braddock</name><affiliation><mods:affiliation>From the Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA</mods:affiliation></affiliation></author><author><name sortKey="Davis, Catharine S" sort="Davis, Catharine S" uniqKey="Davis C" first="Catharine S." last="Davis">Catharine S. Davis</name><affiliation><mods:affiliation>Department of Pediatrics, University of North Carolina Medical School, Chapel Hill, NC, USA</mods:affiliation></affiliation></author><author><name sortKey="Davis, Richard B" sort="Davis, Richard B" uniqKey="Davis R" first="Richard B." last="Davis">Richard B. Davis</name><affiliation><mods:affiliation>From the Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Journal of the American Academy of Dermatology</title><title level="j" type="abbrev">YMJD</title><idno type="ISSN">0190-9622</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1988">1988</date><biblScope unit="volume">19</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="supplement">P1</biblScope><biblScope unit="page" from="859">859</biblScope><biblScope unit="page" to="868">868</biblScope></imprint><idno type="ISSN">0190-9622</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0190-9622</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Abdomen chest</term><term>Alcian</term><term>American academy</term><term>Antimalarial drugs</term><term>Arch dermatol</term><term>Braddock</term><term>Chest chest</term><term>Cutaneous</term><term>Dermal</term><term>Dermatol</term><term>Dermis</term><term>Discoid lupus erythematosus</term><term>Electron microscopy</term><term>Eruption</term><term>Erythematous</term><term>Fibroblast</term><term>Hautkr</term><term>Hyperthyroidism</term><term>Idiopathic</term><term>Idiopathic thrombocytopenic purpura</term><term>Immune</term><term>Immune complexes</term><term>Immune function</term><term>Mucin</term><term>Mucinosis</term><term>Other diseases</term><term>Photosensitivity</term><term>Plaquelike</term><term>Plaquelike cutaneous mucinosis</term><term>Platelet</term><term>Pruritus</term><term>Purpura</term><term>Rash</term><term>Reticular</term><term>Reticular erythematous mucinosis</term><term>Reticular erythematous mucinosis syndrome</term><term>Solar sensitivity</term><term>Solar simulator</term><term>Steigleder</term><term>Syndrome</term><term>Thrombocytopenic</term><term>Thrombocytopenic purpura</term><term>Viral</term><term>World literature</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract">A case of reticular erythematous mucinosis associated with chronic idiopathic thrombocytopenic purpura and circulating immune complexes is described. We compare reticular erythematous mucinosis with the similar plaquelike cutaneous mucinosis. We discuss the apparent photosensitivity of reticular erythematous mucinosis and its possible relationship with altered states of immune function such as diabetes, thyroid disease, and neoplasia. The somewhat varied but characteristic histopathologic findings and staining are reviewed, including the characteristic perivascular and occasional perifollicular lymphocytic infiltrate and Alcian blue-positive dermal mucin. Treatment with antimalarial drugs still appears to be the most uniformly successful therapeutic approach to the management of this chronic dermatosis. 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Braddock M.D.</name><affiliations><json:string>From the Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA</json:string></affiliations></json:item><json:item><name>Catharine S. Davis M.D.</name><affiliations><json:string>Department of Pediatrics, University of North Carolina Medical School, Chapel Hill, NC, USA</json:string></affiliations></json:item><json:item><name>Richard B. Davis M.D.</name><affiliations><json:string>From the Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA</json:string></affiliations></json:item></author><articleId><json:string>80372</json:string></articleId><arkIstex>ark:/67375/6H6-1T69G1WJ-1</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Review article</json:string></originalGenre><abstract>A case of reticular erythematous mucinosis associated with chronic idiopathic thrombocytopenic purpura and circulating immune complexes is described. 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We compare reticular erythematous mucinosis with the similar plaquelike cutaneous mucinosis. We discuss the apparent photosensitivity of reticular erythematous mucinosis and its possible relationship with altered states of immune function such as diabetes, thyroid disease, and neoplasia. The somewhat varied but characteristic histopathologic findings and staining are reviewed, including the characteristic perivascular and occasional perifollicular lymphocytic infiltrate and Alcian blue-positive dermal mucin. Treatment with antimalarial drugs still appears to be the most uniformly successful therapeutic approach to the management of this chronic dermatosis. Further research efforts should be directed at understanding its link with altered states of immune function.</p></abstract></profileDesc><revisionDesc><change when="1988">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-1T69G1WJ-1/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier doc found" wicri:toSee="Elsevier, no converted or simple article"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 5.0.1//EN//XML" URI="art501.dtd" name="istex:docType"></istex:docType><istex:document><article version="5.0" xml:lang="en" docsubtype="rev"><item-info><jid>YMJD</jid><aid>80372</aid><ce:pii>S0190-9622(88)70246-7</ce:pii><ce:doi>10.1016/S0190-9622(88)70246-7</ce:doi><ce:copyright type="unknown" year="1988">American Academy of Dermatology, Inc.</ce:copyright></item-info><head><ce:title>Reticular erythematous mucinosis and thrombocytopenic purpura</ce:title><ce:subtitle>Report of a case and review of the world literature, including plaquelike cutaneous mucinosis</ce:subtitle><ce:author-group><ce:author><ce:given-name>Suzanne W.</ce:given-name><ce:surname>Braddock</ce:surname><ce:degrees>M.D.</ce:degrees><ce:cross-ref refid="cor1"><ce:sup>†</ce:sup></ce:cross-ref><ce:cross-ref refid="aff1"><ce:sup>1</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Catharine S.</ce:given-name><ce:surname>Davis</ce:surname><ce:degrees>M.D.</ce:degrees><ce:cross-ref refid="aff2"><ce:sup>*</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Richard B.</ce:given-name><ce:surname>Davis</ce:surname><ce:degrees>M.D.</ce:degrees><ce:cross-ref refid="aff1"><ce:sup>1</ce:sup></ce:cross-ref></ce:author><ce:affiliation id="aff1"><ce:label>1</ce:label><ce:textfn>From the Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA</ce:textfn></ce:affiliation><ce:affiliation id="aff2"><ce:label>*</ce:label><ce:textfn>Department of Pediatrics, University of North Carolina Medical School, Chapel Hill, NC, USA</ce:textfn></ce:affiliation><ce:correspondence id="cor1"><ce:label>†</ce:label><ce:text>Reprint requests to: Dr. Suzanne Braddock, Dermatology, CH 4010, University of Nebraska Medical Center, 42nd and Dewey Streets, Omaha, NE 68105-1065.</ce:text></ce:correspondence></ce:author-group><ce:abstract id="ab1"><ce:abstract-sec><ce:simple-para>A case of reticular erythematous mucinosis associated with chronic idiopathic thrombocytopenic purpura and circulating immune complexes is described. We compare reticular erythematous mucinosis with the similar plaquelike cutaneous mucinosis. We discuss the apparent photosensitivity of reticular erythematous mucinosis and its possible relationship with altered states of immune function such as diabetes, thyroid disease, and neoplasia. The somewhat varied but characteristic histopathologic findings and staining are reviewed, including the characteristic perivascular and occasional perifollicular lymphocytic infiltrate and Alcian blue-positive dermal mucin. Treatment with antimalarial drugs still appears to be the most uniformly successful therapeutic approach to the management of this chronic dermatosis. Further research efforts should be directed at understanding its link with altered states of immune function.</ce:simple-para></ce:abstract-sec></ce:abstract></head><tail><ce:bibliography><ce:section-title>References</ce:section-title><ce:bibliography-sec><ce:bib-reference id="bib1"><ce:label>1.</ce:label><sb:reference><sb:contribution><sb:authors><sb:author><ce:given-name>HO</ce:given-name><ce:surname>Perry</ce:surname></sb:author><sb:author><ce:given-name>RR</ce:given-name><ce:surname>Kierland</ce:surname></sb:author><sb:author><ce:given-name>H</ce:given-name><ce:surname>Montgomery</ce:surname></sb:author></sb:authors><sb:title><sb:maintitle>Plaque-like form of cutaneous mucinosis</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Arch Dermatol</sb:maintitle></sb:title><sb:volume-nr>82</sb:volume-nr></sb:series><sb:date>1960</sb:date></sb:issue><sb:pages><sb:first-page>980</sb:first-page><sb:last-page>985</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference><ce:bib-reference id="bib2"><ce:label>2.</ce:label><sb:reference><sb:contribution><sb:authors><sb:author><ce:given-name>GK</ce:given-name><ce:surname>Steigleder</ce:surname></sb:author><sb:author><ce:given-name>H</ce:given-name><ce:surname>Gartmann</ce:surname></sb:author><sb:author><ce:given-name>U</ce:given-name><ce:surname>Linker</ce:surname></sb:author></sb:authors><sb:title><sb:maintitle>REM syndrom: retikulare erythematose mucinosis (Rundzellerythema-tosus)</sb:maintitle></sb:title></sb:contribution><sb:host><sb:issue><sb:series><sb:title><sb:maintitle>Z 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Haematol</sb:maintitle></sb:title><sb:volume-nr>55</sb:volume-nr></sb:series><sb:date>1983</sb:date></sb:issue><sb:pages><sb:first-page>533</sb:first-page><sb:last-page>545</sb:last-page></sb:pages></sb:host></sb:reference></ce:bib-reference></ce:bibliography-sec></ce:bibliography></tail></article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Reticular erythematous mucinosis and thrombocytopenic purpura</title><subTitle>Report of a case and review of the world literature, including plaquelike cutaneous mucinosis</subTitle></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>Reticular erythematous mucinosis and thrombocytopenic purpura</title><subTitle>Report of a case and review of the world literature, including plaquelike cutaneous mucinosis</subTitle></titleInfo><name type="personal"><namePart type="given">Suzanne W.</namePart><namePart type="family">Braddock</namePart><namePart type="termsOfAddress">M.D.</namePart><affiliation>From the Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA</affiliation><description>Reprint requests to: Dr. Suzanne Braddock, Dermatology, CH 4010, University of Nebraska Medical Center, 42nd and Dewey Streets, Omaha, NE 68105-1065.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Catharine S.</namePart><namePart type="family">Davis</namePart><namePart type="termsOfAddress">M.D.</namePart><affiliation>Department of Pediatrics, University of North Carolina Medical School, Chapel Hill, NC, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Richard B.</namePart><namePart type="family">Davis</namePart><namePart type="termsOfAddress">M.D.</namePart><affiliation>From the Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article" displayLabel="Review article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-L5L7X3NF-P">review-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1988</dateIssued><copyrightDate encoding="w3cdtf">1988</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract>A case of reticular erythematous mucinosis associated with chronic idiopathic thrombocytopenic purpura and circulating immune complexes is described. We compare reticular erythematous mucinosis with the similar plaquelike cutaneous mucinosis. We discuss the apparent photosensitivity of reticular erythematous mucinosis and its possible relationship with altered states of immune function such as diabetes, thyroid disease, and neoplasia. The somewhat varied but characteristic histopathologic findings and staining are reviewed, including the characteristic perivascular and occasional perifollicular lymphocytic infiltrate and Alcian blue-positive dermal mucin. Treatment with antimalarial drugs still appears to be the most uniformly successful therapeutic approach to the management of this chronic dermatosis. Further research efforts should be directed at understanding its link with altered states of immune function.</abstract><relatedItem type="host"><titleInfo><title>Journal of the American Academy of Dermatology</title></titleInfo><titleInfo type="abbreviated"><title>YMJD</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><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1988</dateIssued></originInfo><identifier type="ISSN">0190-9622</identifier><identifier type="PII">S0190-9622(05)X7113-4</identifier><part><date>1988</date><detail type="volume"><number>19</number><caption>vol.</caption></detail><detail type="issue"><number>5</number><caption>no.</caption></detail><detail type="supplement"><number>P1</number><caption>Suppl.</caption></detail><extent unit="issue-pages"><start>767</start><end>928</end></extent><extent unit="pages"><start>859</start><end>868</end></extent></part></relatedItem><identifier type="istex">DA2BB316F69C20EB9E106EA3640EB7DEE2F279DF</identifier><identifier type="ark">ark:/67375/6H6-1T69G1WJ-1</identifier><identifier type="DOI">10.1016/S0190-9622(88)70246-7</identifier><identifier type="PII">S0190-9622(88)70246-7</identifier><identifier type="ArticleID">80372</identifier><accessCondition type="use and reproduction" contentType="copyright">©1988 American Academy of Dermatology, Inc.</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource><recordOrigin>American Academy of Dermatology, Inc., ©1988</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-1T69G1WJ-1/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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