{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,12]],"date-time":"2026-11-12T06:08:31Z","timestamp":1794463711394,"version":"4.9.1"},"reference-count":39,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2012,9,14]],"date-time":"2012-09-14T00:00:00Z","timestamp":1347580800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["The Journal of Dermatology"],"published-print":{"date-parts":[[2012,12]]},"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:p>Pyoderma gangrenosum (<jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content>) is an ulcerative skin disorder characterized by neutrophilic infiltrations. <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content> is generally classified into four types: (i) ulcerative; (ii) pustular; (iii) bullous; and (iv) vegetative. Among them, bullous <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content> is known as a rare type. Herein, we report a case of bullous <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content> together with a summary of the 12 <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content> cases treated in our department over the previous 15\u00a0years, and we review 38 well\u2010documented bullous <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content> cases (65.8% female; aged 18\u201380\u00a0years [mean\u00a0\u00b1\u00a0standard deviation, 51.6\u00a0\u00b1\u00a016.8]) in the published work, including the present case, from 1972\u20132011. Although the disease most frequently associated with <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content> is inflammatory bowel disease, bullous <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content> is most commonly associated with hematological disorders (25\/38, 65.8%), which indicates the characteristic pathophysiology specific to bullous <jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/j.1346-8138.2012.01676.x","type":"journal-article","created":{"date-parts":[[2012,9,15]],"date-time":"2012-09-15T02:52:44Z","timestamp":1347677564000},"page":"1010-1015","source":"Crossref","is-referenced-by-count":31,"title":["Bullous pyoderma gangrenosum: A case report and review of the published work"],"prefix":"10.1111","volume":"39","author":[{"given":"Masayuki","family":"Sakiyama","sequence":"first","affiliation":[{"name":"Department of Dermatology National Defense Medical College Tokorozawa Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Takashi","family":"Kobayashi","sequence":"additional","affiliation":[{"name":"Department of Dermatology National Defense Medical College Tokorozawa Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuiko","family":"Nagata","sequence":"additional","affiliation":[{"name":"Department of Dermatology National Defense Medical College Tokorozawa Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Norihiro","family":"Fujimoto","sequence":"additional","affiliation":[{"name":"Department of Dermatology National Defense Medical College Tokorozawa Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Takahiro","family":"Satoh","sequence":"additional","affiliation":[{"name":"Department of Dermatology National Defense Medical College Tokorozawa 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