{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,6]],"date-time":"2026-01-06T05:21:20Z","timestamp":1767676880812,"version":"3.40.4"},"reference-count":15,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2018,3,19]]},"abstract":"<jats:p>Pemphigoid gestationis (PG), also known as<jats:italic>herpes gestationis<\/jats:italic>, is a rare autoimmune blistering disease specific to pregnancy, which usually presents in the second or third trimesters and, in 15%\u201325% of cases, during the immediate postpartum period.<jats:sup>1<\/jats:sup>Although the ethiopathogeny of PG is not fully clarified, most patients develop antibodies against a 180\u2009kDa transmembrane hemidesmosomal protein (BP180; BPAG2; collagen XVII).<jats:sup>2<\/jats:sup>PG has a strong association with human leucocyte antigens DR3 and DR4.<jats:sup>3<\/jats:sup><\/jats:p><jats:p>We report a case of a 29-year-old female patient with PG successfully treated with intravenous immunoglobulin.<\/jats:p>","DOI":"10.1136\/bcr-2018-224346","type":"journal-article","created":{"date-parts":[[2018,4,7]],"date-time":"2018-04-07T14:25:11Z","timestamp":1523111111000},"page":"bcr-2018-224346","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":8,"title":["Pemphigoid gestationis successfully treated with intravenous immunoglobulin"],"prefix":"10.1136","volume":"2018","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6561-5338","authenticated-orcid":false,"given":"Filipa 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