Paraneoplastic pemphigus with negative direct immunofluorescence in epidermis or mucosa but positive findings in adnexal structures
Introduction: Paraneoplastic pemphigus (PNP) is considered an autoimmune, multiorgan disease caused by antiplakin antibodies. We present three PNP patients who had negative epithelial direct immunofluorescence (DIF) findings in one or more biopsies. Patients: An early lip biopsy of uninvolved oral...
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description | Introduction: Paraneoplastic pemphigus (PNP) is considered an autoimmune, multiorgan disease caused by antiplakin antibodies. We present three PNP patients who had negative epithelial direct immunofluorescence (DIF) findings in one or more biopsies.
Patients: An early lip biopsy of uninvolved oral epithelia in patient 1 was negative. A later biopsy from foreskin showed intense intercellular immunoglobulin G (IgG) deposits in the epithelia. In the early phase of the disease in patient 2, the intercellular fluorescence was negative in the epidermis, while intercellular IgG and C3 were observed in the sweat ducts. A later biopsy showed weak intercellular epidermal IgG and C3 fluorescence. Patient 3 showed intercellular IgG and/or C3 in follicular, sebaceous and sweat duct structures in several biopsies. No intercellular IgG or C3 was observed in the epithelia.
Discussion: The presence of immunoreactants in adnexal structures suggests that desmoplakins can be more strongly expressed in adnexa than in the epidermis, facilitating visualization of antibody deposits.
Conclusions: Negative DIF findings in epithelia do not rule out the diagnosis of PNP, and the presence of IgG and/or C3 at the intercellular level of adnexal structures can help establish this diagnosis. |
doi_str_mv | 10.1111/j.1600-0560.2008.00993.x |
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Patients: An early lip biopsy of uninvolved oral epithelia in patient 1 was negative. A later biopsy from foreskin showed intense intercellular immunoglobulin G (IgG) deposits in the epithelia. In the early phase of the disease in patient 2, the intercellular fluorescence was negative in the epidermis, while intercellular IgG and C3 were observed in the sweat ducts. A later biopsy showed weak intercellular epidermal IgG and C3 fluorescence. Patient 3 showed intercellular IgG and/or C3 in follicular, sebaceous and sweat duct structures in several biopsies. No intercellular IgG or C3 was observed in the epithelia.
Discussion: The presence of immunoreactants in adnexal structures suggests that desmoplakins can be more strongly expressed in adnexa than in the epidermis, facilitating visualization of antibody deposits.
Conclusions: Negative DIF findings in epithelia do not rule out the diagnosis of PNP, and the presence of IgG and/or C3 at the intercellular level of adnexal structures can help establish this diagnosis.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/j.1600-0560.2008.00993.x</identifier><identifier>PMID: 18564282</identifier><identifier>CODEN: JCUPBN</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Autoantibodies - analysis ; Autoantibodies - immunology ; Autoantigens - immunology ; Autoimmune Diseases - immunology ; Autoimmune Diseases - pathology ; Biological and medical sciences ; Bullous diseases of the skin ; Complement C3 - analysis ; Complement C3 - immunology ; Dermatology ; Desmoplakins - immunology ; Female ; Fluorescent Antibody Technique, Direct ; Humans ; Immunoglobulin G - analysis ; Immunoglobulin G - immunology ; Male ; Medical sciences ; Middle Aged ; Paraneoplastic Syndromes - immunology ; Paraneoplastic Syndromes - pathology ; Pemphigus - immunology ; Pemphigus - pathology ; Sweat Glands - immunology ; Sweat Glands - pathology</subject><ispartof>Journal of cutaneous pathology, 2009-01, Vol.36 (1), p.34-38</ispartof><rights>2008 John Wiley & Sons A/S</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4343-fc837fbbbd317513c71bc08565832aa1b9717d780ecb88469077f1a50f265c03</citedby><cites>FETCH-LOGICAL-c4343-fc837fbbbd317513c71bc08565832aa1b9717d780ecb88469077f1a50f265c03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1600-0560.2008.00993.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-0560.2008.00993.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,4012,27906,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20976310$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18564282$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barnadas, Maria A.</creatorcontrib><creatorcontrib>Curell, Román</creatorcontrib><creatorcontrib>Alomar, Agustín</creatorcontrib><creatorcontrib>Gelpí, Carmen</creatorcontrib><title>Paraneoplastic pemphigus with negative direct immunofluorescence in epidermis or mucosa but positive findings in adnexal structures</title><title>Journal of cutaneous pathology</title><addtitle>J Cutan Pathol</addtitle><description>Introduction: Paraneoplastic pemphigus (PNP) is considered an autoimmune, multiorgan disease caused by antiplakin antibodies. We present three PNP patients who had negative epithelial direct immunofluorescence (DIF) findings in one or more biopsies.
Patients: An early lip biopsy of uninvolved oral epithelia in patient 1 was negative. A later biopsy from foreskin showed intense intercellular immunoglobulin G (IgG) deposits in the epithelia. In the early phase of the disease in patient 2, the intercellular fluorescence was negative in the epidermis, while intercellular IgG and C3 were observed in the sweat ducts. A later biopsy showed weak intercellular epidermal IgG and C3 fluorescence. Patient 3 showed intercellular IgG and/or C3 in follicular, sebaceous and sweat duct structures in several biopsies. No intercellular IgG or C3 was observed in the epithelia.
Discussion: The presence of immunoreactants in adnexal structures suggests that desmoplakins can be more strongly expressed in adnexa than in the epidermis, facilitating visualization of antibody deposits.
Conclusions: Negative DIF findings in epithelia do not rule out the diagnosis of PNP, and the presence of IgG and/or C3 at the intercellular level of adnexal structures can help establish this diagnosis.</description><subject>Aged</subject><subject>Autoantibodies - analysis</subject><subject>Autoantibodies - immunology</subject><subject>Autoantigens - immunology</subject><subject>Autoimmune Diseases - immunology</subject><subject>Autoimmune Diseases - pathology</subject><subject>Biological and medical sciences</subject><subject>Bullous diseases of the skin</subject><subject>Complement C3 - analysis</subject><subject>Complement C3 - immunology</subject><subject>Dermatology</subject><subject>Desmoplakins - immunology</subject><subject>Female</subject><subject>Fluorescent Antibody Technique, Direct</subject><subject>Humans</subject><subject>Immunoglobulin G - analysis</subject><subject>Immunoglobulin G - immunology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Paraneoplastic Syndromes - immunology</subject><subject>Paraneoplastic Syndromes - pathology</subject><subject>Pemphigus - immunology</subject><subject>Pemphigus - pathology</subject><subject>Sweat Glands - immunology</subject><subject>Sweat Glands - pathology</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtv1DAURi0EokPhLyBvYJdwHSe2I7GBER2QKhihoi4tx3GmHvLCDzpd88dxOqNhize25PPdx0EIE8hJOu_2OWEAGVQM8gJA5AB1TfPDE7Q6fzxFK6BAM1YLfoFeeL8HIEyw6jm6IKJiZSGKFfqzVU6NZpp75YPVeDbDfGd30eN7G-7waHYq2N8Gt9YZHbAdhjhOXR8nZ7w2ozbYjtjMtjVusB5PDg9RT17hJgY8T94-pjs7tnbc-QVW7WgOqsc-uKhDTHVeomed6r15dbov0c3Vp5v15-z62-bL-sN1pkta0qzTgvKuaZqWEl4RqjlpNKRNKkELpUhTc8JbLsDoRoiS1cB5R1QFXcEqDfQSvT2Wnd30KxofZJpYm75f9o9eMsZrXlKSQHEEtZu8d6aTs7ODcg-SgFz8y71cNMtFs1z8y0f_8pCir089YjOY9l_wJDwBb06A8lr1XZKvrT9zBdScUbIM-_7I3dvePPz3AHL9Y5seKZ4d49YHczjHlfspGae8krdfN_L71S1j281afqR_AQKVsvU</recordid><startdate>200901</startdate><enddate>200901</enddate><creator>Barnadas, Maria A.</creator><creator>Curell, Román</creator><creator>Alomar, Agustín</creator><creator>Gelpí, Carmen</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200901</creationdate><title>Paraneoplastic pemphigus with negative direct immunofluorescence in epidermis or mucosa but positive findings in adnexal structures</title><author>Barnadas, Maria A. ; Curell, Román ; Alomar, Agustín ; Gelpí, Carmen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4343-fc837fbbbd317513c71bc08565832aa1b9717d780ecb88469077f1a50f265c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Autoantibodies - analysis</topic><topic>Autoantibodies - immunology</topic><topic>Autoantigens - immunology</topic><topic>Autoimmune Diseases - immunology</topic><topic>Autoimmune Diseases - pathology</topic><topic>Biological and medical sciences</topic><topic>Bullous diseases of the skin</topic><topic>Complement C3 - analysis</topic><topic>Complement C3 - immunology</topic><topic>Dermatology</topic><topic>Desmoplakins - immunology</topic><topic>Female</topic><topic>Fluorescent Antibody Technique, Direct</topic><topic>Humans</topic><topic>Immunoglobulin G - analysis</topic><topic>Immunoglobulin G - immunology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Paraneoplastic Syndromes - immunology</topic><topic>Paraneoplastic Syndromes - pathology</topic><topic>Pemphigus - immunology</topic><topic>Pemphigus - pathology</topic><topic>Sweat Glands - immunology</topic><topic>Sweat Glands - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barnadas, Maria A.</creatorcontrib><creatorcontrib>Curell, Román</creatorcontrib><creatorcontrib>Alomar, Agustín</creatorcontrib><creatorcontrib>Gelpí, Carmen</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barnadas, Maria A.</au><au>Curell, Román</au><au>Alomar, Agustín</au><au>Gelpí, Carmen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Paraneoplastic pemphigus with negative direct immunofluorescence in epidermis or mucosa but positive findings in adnexal structures</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>2009-01</date><risdate>2009</risdate><volume>36</volume><issue>1</issue><spage>34</spage><epage>38</epage><pages>34-38</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><coden>JCUPBN</coden><abstract>Introduction: Paraneoplastic pemphigus (PNP) is considered an autoimmune, multiorgan disease caused by antiplakin antibodies. We present three PNP patients who had negative epithelial direct immunofluorescence (DIF) findings in one or more biopsies.
Patients: An early lip biopsy of uninvolved oral epithelia in patient 1 was negative. A later biopsy from foreskin showed intense intercellular immunoglobulin G (IgG) deposits in the epithelia. In the early phase of the disease in patient 2, the intercellular fluorescence was negative in the epidermis, while intercellular IgG and C3 were observed in the sweat ducts. A later biopsy showed weak intercellular epidermal IgG and C3 fluorescence. Patient 3 showed intercellular IgG and/or C3 in follicular, sebaceous and sweat duct structures in several biopsies. No intercellular IgG or C3 was observed in the epithelia.
Discussion: The presence of immunoreactants in adnexal structures suggests that desmoplakins can be more strongly expressed in adnexa than in the epidermis, facilitating visualization of antibody deposits.
Conclusions: Negative DIF findings in epithelia do not rule out the diagnosis of PNP, and the presence of IgG and/or C3 at the intercellular level of adnexal structures can help establish this diagnosis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18564282</pmid><doi>10.1111/j.1600-0560.2008.00993.x</doi><tpages>5</tpages></addata></record> |
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subjects | Aged Autoantibodies - analysis Autoantibodies - immunology Autoantigens - immunology Autoimmune Diseases - immunology Autoimmune Diseases - pathology Biological and medical sciences Bullous diseases of the skin Complement C3 - analysis Complement C3 - immunology Dermatology Desmoplakins - immunology Female Fluorescent Antibody Technique, Direct Humans Immunoglobulin G - analysis Immunoglobulin G - immunology Male Medical sciences Middle Aged Paraneoplastic Syndromes - immunology Paraneoplastic Syndromes - pathology Pemphigus - immunology Pemphigus - pathology Sweat Glands - immunology Sweat Glands - pathology |
title | Paraneoplastic pemphigus with negative direct immunofluorescence in epidermis or mucosa but positive findings in adnexal structures |
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