{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,28]],"date-time":"2025-09-28T11:05:17Z","timestamp":1759057517909},"reference-count":12,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2014,8,11]],"date-time":"2014-08-11T00:00:00Z","timestamp":1407715200000},"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":[[2014,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Familial Mediterranean Fever (<jats:styled-content style=\"fixed-case\">FMF<\/jats:styled-content>) is a hereditary autoinflammatory disease, which is characterized by recurrent and paroxysmal fever, peritonitis, arthritis, myalgia, and skin rashes. Although various skin lesions such as \u201cerysipelas\u2010like erythema\u201d, urticaria, nonspecific purpura, and subcutaneous nodules have been described, cutaneous vasculitis is rare. We report a Japanese case of sporadic <jats:styled-content style=\"fixed-case\">FMF<\/jats:styled-content> accompanied by cutaneous arteritis at the time of febrile attacks of <jats:styled-content style=\"fixed-case\">FMF<\/jats:styled-content>. Gene analysis revealed M694I mutation in a single allele of the <jats:italic><jats:styled-content style=\"fixed-case\">MEFV<\/jats:styled-content><\/jats:italic> gene, and oral colchicine successfully controlled both periodic fever and subcutaneous nodules of arteritis. Cutaneous necrotizing vasculitis repeatedly emerging with febrile attacks should be included among the skin manifestations of <jats:styled-content style=\"fixed-case\">FMF<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/1346-8138.12588","type":"journal-article","created":{"date-parts":[[2014,8,11]],"date-time":"2014-08-11T09:58:11Z","timestamp":1407751091000},"page":"827-829","source":"Crossref","is-referenced-by-count":11,"title":["Cutaneous necrotizing vasculitis as a manifestation of familial <scp>M<\/scp>editerranean fever"],"prefix":"10.1111","volume":"41","author":[{"given":"Shigetsuna","family":"Komatsu","sequence":"first","affiliation":[{"name":"Department of Dermatology Asahikawa Medical University Asahikawa Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masaru","family":"Honma","sequence":"additional","affiliation":[{"name":"Department of Dermatology Asahikawa Medical University Asahikawa 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Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,8,11]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(97)09408-7"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1097\/MD.0b013e318277cf75"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2249.2011.04438.x"},{"key":"e_1_2_5_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9343(67)90167-2"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/art.1780401023"},{"key":"e_1_2_5_7_1","doi-asserted-by":"publisher","DOI":"10.1097\/00005792-200209000-00002"},{"key":"e_1_2_5_8_1","doi-asserted-by":"publisher","DOI":"10.1067\/mjd.2000.103048"},{"key":"e_1_2_5_9_1","first-page":"323","article-title":"Vasculitis in familial Mediterranean fever","volume":"24","author":"Ozdogan H","year":"1997","journal-title":"J 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