{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,19]],"date-time":"2026-08-19T19:14:39Z","timestamp":1787166879790,"version":"build-2736575974"},"reference-count":39,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2013,3,12]],"date-time":"2013-03-12T00:00:00Z","timestamp":1363046400000},"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":[[2013,6]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Eosinophilic pustular folliculitis (\n                    <jats:styled-content style=\"fixed-case\">EPF<\/jats:styled-content>\n                    ) is an inflammatory disease characterized by repeated pruritic follicular papules and pustules arranged in arcuate plaques, and folliculotropic infiltration of eosinophils. The diagnosis of\n                    <jats:styled-content style=\"fixed-case\">EPF<\/jats:styled-content>\n                    is occasionally difficult and problematic because\n                    <jats:styled-content style=\"fixed-case\">EPF<\/jats:styled-content>\n                    may share the clinical appearance and histological findings with other diseases. Moreover,\n                    <jats:styled-content style=\"fixed-case\">EPF<\/jats:styled-content>\n                    has several clinical subtypes, including the classical type, infantile type and immunosuppression\u2010associated type. Because the therapies of\n                    <jats:styled-content style=\"fixed-case\">EPF<\/jats:styled-content>\n                    are relatively specific as compared to eczematous disorders, accurate diagnosis is essential for the management of\n                    <jats:styled-content style=\"fixed-case\">EPF<\/jats:styled-content>\n                    . Clinical differential diagnoses include tinea, acne, rosacea, eczematous dermatitis, granuloma faciale, autoimmune annular erythema, infestations and pustular dermatosis. Histologically, cutaneous diseases with eosinophilic infiltrates can be differentially diagnosed. Follicular mucinosis, mycosis fungoides and other cutaneous\n                    <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>\n                    \u2010cell lymphomas are the most important differential diagnoses both clinically and histopathologically. It should be kept in mind particularly that the initial lesions of cutaneous\n                    <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>\n                    \u2010cell lymphoma resemble\n                    <jats:styled-content style=\"fixed-case\">EPF<\/jats:styled-content>\n                    .\n                  <\/jats:p>","DOI":"10.1111\/1346-8138.12125","type":"journal-article","created":{"date-parts":[[2013,3,13]],"date-time":"2013-03-13T20:34:54Z","timestamp":1363206894000},"page":"419-423","source":"Crossref","is-referenced-by-count":44,"title":["Clinical and histopathological differential diagnosis of eosinophilic pustular folliculitis"],"prefix":"10.1111","volume":"40","author":[{"given":"Toshiharu","family":"Fujiyama","sequence":"first","affiliation":[{"name":"Department of Dermatology Hamamatsu University School of Medicine Hamamatsu 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