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<xml><records><record><database name="MyLibrary">MyLibrary</database><source-app name="Zotero">Zotero</source-app><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Diabaté, Almamy</author><author>Naqi, Ali</author><author>Pittoni, Julien</author></authors></contributors><titles><title>Atypical paraneoplastic pemphigus associated with pulmonary adenocarcinoma</title><secondary-title>Our Dermatology Online</secondary-title></titles><periodical><full-title>Our Dermatology Online</full-title></periodical><pages>349-351</pages><volume>10</volume><number>4</number><issue>4</issue><dates><year>2019</year><pub-dates><date>2019-10-03</date></pub-dates></dates><isbn>20819390</isbn><electronic-resource-num>10.7241/ourd.20194.7</electronic-resource-num><abstract>Paraneoplastic pemphigus (PNP) is a muco-cutaneous autoimmune disease associated with several types of internal malignancy. We report a case of a 57-year-old male with an atypical form of PNP associated with pulmonary adenocarcinoma. There was no involvement of the mucous membranes. Although the macroscopic and histological appearances were typical of a pemphigus, the direct immunofluorescence was positive for the IgG staining and the C3 intercellular. Circulating antibodies were detected with envoplakin, periplakin and desmoplakins 1 and 2; but the Ac anti desmoglein 1 IgG and 3 IgG, BP 180 and BP 230 and auto Ac anti-epidermis were negative. The clinical evolvement was observed with a combination of systemic corticosteroids and radiotherapy associated with Cisplatin-Alimta chemotherapy.</abstract><remote-database-name>Crossref</remote-database-name><language>en</language><urls><web-urls><url>http://www.odermatol.com/issue-in-html/2019-4-7-pemphigus/</url></web-urls><pdf-urls><url>D:\OurDermatolOnline\2019\numer 2019 4\pdf\7.Atypical-DiabateA.pdf</url></pdf-urls></urls><access-date>2019-10-12 11:37:45</access-date></record></records></xml>