{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,19]],"date-time":"2026-08-19T05:48:39Z","timestamp":1787118519326,"version":"build-2736575974"},"reference-count":17,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2022,1,20]],"date-time":"2022-01-20T00:00:00Z","timestamp":1642636800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Int J Dermatology"],"published-print":{"date-parts":[[2022,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Brunsting\u2010Perry pemphigoid (BPP) is a rare, autoimmune bullous skin disorder classified within the spectrum of mucous membrane pemphigoid (MMP).<\/jats:p><\/jats:sec><jats:sec><jats:title>Materials and Methods<\/jats:title><jats:p>An <jats:italic>a priori<\/jats:italic> protocol was designed based on PRISMA guidelines. PubMed and Scopus databases were searched for English\u2010language articles concerning BPP published between 1950 and July 2021.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Thirty\u2010six articles including 63 BPP patients were analyzed. The mean age at diagnosis was 62.9\u2009years (range: 27\u201086). BPP was shown to be characterized by vesiculobullous lesions (46\/63, 73.0%) on an erythematous base, erosions or ulcerations (27\/63, 42.9%), atrophic scars (49\/63, 77.8%), and milia (4\/63, 6.3%). Exclusive oral mucosal involvement was documented in 22.2% of cases, usually manifesting after the cutaneous onset of the disease. Subepidermal blistering was a constant finding, often with an eosinophil\u2010rich inflammatory infiltrate (21\/58, 36.2%). Positive direct immunofluorescence was found in 92.0% of patients, almost always with linear IgG\u2009\u00b1\u2009C3 deposits along the basement membrane (43\/46, 93.5%). BP180 (12\/15, 80.0%), BP230 (5\/15, 33.3%), and laminin 332 (3\/15, 20.0%) were the most frequently identified target antigens.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>BPP nosologic position remains uncertain, given the overlap with other autoimmune bullous diseases, such as MMP, bullous pemphigoid, and epidermolysis bullosa acquisita, particularly in its BPP\u2010like variant. Nonpredominant oral mucosal lesions may appear during the course of the disease, generally after cutaneous manifestations. Positivity of DIF and anti\u2010BP180\/230 autoantibodies detected on ELISA\/immunoblotting in the absence of anticollagen VII antibodies may provide guidance in diagnosing BPP.<\/jats:p><\/jats:sec>","DOI":"10.1111\/ijd.16045","type":"journal-article","created":{"date-parts":[[2022,1,20]],"date-time":"2022-01-20T11:39:37Z","timestamp":1642678777000},"page":"1353-1358","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":22,"title":["Brunsting\u2010Perry pemphigoid: a systematic review"],"prefix":"10.1111","volume":"61","author":[{"given":"Italo Francesco","family":"Aromolo","sequence":"first","affiliation":[{"name":"Dermatology Unit Fondazione IRCCS Ca\u2019 Granda Ospedale Maggiore Policlinico Milan Italy"},{"name":"Department of Pathophysiology and Transplantation Universit\u00e0 degli Studi di Milano Milan 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