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Dermatomyositis in patients with autoimmune blistering diseases☆☆☆

Identifieur interne : 000A37 ( Pmc/Curation ); précédent : 000A36; suivant : 000A38

Dermatomyositis in patients with autoimmune blistering diseases☆☆☆

Auteurs : Aikaterini Patsatsi ; David R. Pearson ; Victoria P. Werth

Source :

RBID : PMC:6831793

Abstract

It is common for multiple autoimmune diseases to occur in the same patient. However, autoimmune blistering diseases (AIBD) do not commonly associate with dermatomyositis (DM). We performed a literature review and found 12 previous reports that may be attributed to misdiagnosis, underreporting, or true rarity of association. Herein, we present a case of pemphigus vulgaris and a case of mucous membrane pemphigoid associated with DM and review the related literature. AIBD-associated interstitial lung disease, genetic predisposition, potential environmental triggers of both AIBD and DM, drug-related triggers, and paraneoplastic processes are discussed. Dermatologists must be vigilant for a second autoimmune disease in patients with AIBD that may have therapeutic implications.


Url:
DOI: 10.1016/j.ijwd.2019.05.009
PubMed: 31700982
PubMed Central: 6831793

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PMC:6831793

Le document en format XML

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<title xml:lang="en">Dermatomyositis in patients with autoimmune blistering diseases
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<xref ref-type="fn" rid="d31e671">☆☆</xref>
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<name sortKey="Patsatsi, Aikaterini" sort="Patsatsi, Aikaterini" uniqKey="Patsatsi A" first="Aikaterini" last="Patsatsi">Aikaterini Patsatsi</name>
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<xref ref-type="fn" rid="d31e671">☆☆</xref>
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<p>It is common for multiple autoimmune diseases to occur in the same patient. However, autoimmune blistering diseases (AIBD) do not commonly associate with dermatomyositis (DM). We performed a literature review and found 12 previous reports that may be attributed to misdiagnosis, underreporting, or true rarity of association. Herein, we present a case of pemphigus vulgaris and a case of mucous membrane pemphigoid associated with DM and review the related literature. AIBD-associated interstitial lung disease, genetic predisposition, potential environmental triggers of both AIBD and DM, drug-related triggers, and paraneoplastic processes are discussed. Dermatologists must be vigilant for a second autoimmune disease in patients with AIBD that may have therapeutic implications.</p>
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<journal-id journal-id-type="nlm-ta">Int J Womens Dermatol</journal-id>
<journal-id journal-id-type="iso-abbrev">Int J Womens Dermatol</journal-id>
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<journal-title>International Journal of Women's Dermatology</journal-title>
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<article-title>Dermatomyositis in patients with autoimmune blistering diseases
<sup>
<xref ref-type="fn" rid="d31e663"></xref>
</sup>
<sup>
<xref ref-type="fn" rid="d31e671">☆☆</xref>
</sup>
</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" id="au0005">
<name>
<surname>Patsatsi</surname>
<given-names>Aikaterini</given-names>
</name>
<email>apatsats@auth.gr</email>
<xref rid="cr0005" ref-type="corresp"></xref>
</contrib>
<contrib contrib-type="author" id="au0010">
<name>
<surname>Pearson</surname>
<given-names>David R.</given-names>
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<contrib contrib-type="author" id="au0015">
<name>
<surname>Werth</surname>
<given-names>Victoria P.</given-names>
</name>
</contrib>
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<aff id="af0005">Corporal Michael J. Crescenz VAMC, Philadelphia, Pennsylvania</aff>
<aff id="af0010">Department of Dermatology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania</aff>
<author-notes>
<corresp id="cr0005">
<label></label>
Corresponding Author.
<email>apatsats@auth.gr</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release">
<day>04</day>
<month>6</month>
<year>2019</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="collection">
<month>9</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>04</day>
<month>6</month>
<year>2019</year>
</pub-date>
<volume>5</volume>
<issue>4</issue>
<fpage>256</fpage>
<lpage>260</lpage>
<history>
<date date-type="received">
<day>26</day>
<month>12</month>
<year>2018</year>
</date>
<date date-type="rev-recd">
<day>16</day>
<month>4</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>24</day>
<month>5</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>© 2019 Published by Elsevier Inc. on behalf of Women's Dermatologic Society.</copyright-statement>
<copyright-year>2019</copyright-year>
<copyright-holder></copyright-holder>
<license license-type="CC BY-NC-ND" xlink:href="http://creativecommons.org/licenses/by-nc-nd/4.0/">
<license-p>This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).</license-p>
</license>
</permissions>
<abstract id="ab0005">
<p>It is common for multiple autoimmune diseases to occur in the same patient. However, autoimmune blistering diseases (AIBD) do not commonly associate with dermatomyositis (DM). We performed a literature review and found 12 previous reports that may be attributed to misdiagnosis, underreporting, or true rarity of association. Herein, we present a case of pemphigus vulgaris and a case of mucous membrane pemphigoid associated with DM and review the related literature. AIBD-associated interstitial lung disease, genetic predisposition, potential environmental triggers of both AIBD and DM, drug-related triggers, and paraneoplastic processes are discussed. Dermatologists must be vigilant for a second autoimmune disease in patients with AIBD that may have therapeutic implications.</p>
</abstract>
<kwd-group id="ks0005">
<title>Keywords</title>
<kwd>Dermatomyositis</kwd>
<kwd>interstitial lung disease</kwd>
<kwd>pemphigus</kwd>
<kwd>pemphigoid</kwd>
<kwd>autoimmune</kwd>
<kwd>blistering</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
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}}

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HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Curation/RBID.i   -Sk "pubmed:31700982" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Curation/biblio.hfd   \
       | NlmPubMed2Wicri -a ChloroquineV1 

Wicri

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