{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,26]],"date-time":"2023-09-26T18:43:53Z","timestamp":1695753833698},"reference-count":14,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2015,5,11]],"date-time":"2015-05-11T00:00:00Z","timestamp":1431302400000},"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":[[2015,9]]},"abstract":"Abstract<\/jats:title>Familial Mediterranean fever (FMF<\/jats:styled-content>) is characterized by self\u2010limited bouts of fever and polyserositis. Skin involvement is not common in FMF<\/jats:styled-content>, and erysipelas\u2010like erythema is found to be the most frequent skin eruption which is often accompanied by arthritis and fever, and disappears within 12\u201372\u00a0h. We report a 40\u2010year\u2010old Japanese woman who presented with a 2\u2010year history of recurrent fever with general fatigue, polyarthralgia and transient maculopapular eruptions on her lower extremities and trunk. The histological findings of the maculopapular eruption showed lymphocyte infiltration around the capillaries in the entire dermis. Mutation analysis showed a heterozygous E148Q\u2010P369S mutation of MEFV<\/jats:styled-content><\/jats:italic>. These findings suggested a diagnosis of late\u2010onset FMF<\/jats:styled-content> variant with atypical skin eruptions. The patient was successfully treated with colchicine. Thus, we should pay attention to repeated atypical skin eruptions for the early detection of atypical FMF<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/1346-8138.12929","type":"journal-article","created":{"date-parts":[[2015,5,11]],"date-time":"2015-05-11T05:53:04Z","timestamp":1431323584000},"page":"903-905","source":"Crossref","is-referenced-by-count":6,"title":["Familial Mediterranean fever variant with repeated atypical skin eruptions"],"prefix":"10.1111","volume":"42","author":[{"given":"Tomoko","family":"Takahashi","sequence":"first","affiliation":[{"name":"Department of Dermatology Gifu University Graduate School of Medicine Gifu Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tomomi","family":"Fujisawa","sequence":"additional","affiliation":[{"name":"Department of Dermatology Gifu University Graduate School of Medicine Gifu Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masaki","family":"Kimura","sequence":"additional","affiliation":[{"name":"Department of General and Cardiothoracic Surgery Gifu University Graduate School of Medicine Gifu Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hidenori","family":"Ohnishi","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Gifu University Graduate School of Medicine Gifu Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mariko","family":"Seishima","sequence":"additional","affiliation":[{"name":"Department of Dermatology Gifu University Graduate School of Medicine Gifu Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2015,5,11]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/art.1780401023"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1093\/qjmed\/90.1.37"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1007\/s10067-009-1138-7"},{"key":"e_1_2_5_5_1","doi-asserted-by":"publisher","DOI":"10.1097\/MD.0000000000000029"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00296-009-1073-6"},{"key":"e_1_2_5_7_1","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1096-8628(19991105)87:1<30::AID-AJMG6>3.0.CO;2-B"},{"key":"e_1_2_5_8_1","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.143.8.1080"},{"key":"e_1_2_5_9_1","doi-asserted-by":"publisher","DOI":"10.1093\/rheumatology\/keq157"},{"key":"e_1_2_5_10_1","doi-asserted-by":"publisher","DOI":"10.1097\/MD.0b013e318277cf75"},{"key":"e_1_2_5_11_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11033-009-9543-1"},{"key":"e_1_2_5_12_1","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.134.8.929"},{"key":"e_1_2_5_13_1","doi-asserted-by":"publisher","DOI":"10.1067\/mjd.2000.103048"},{"key":"e_1_2_5_14_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2012.09.038"},{"key":"e_1_2_5_15_1","first-page":"607","article-title":"The cutaneous manifestations in children with familial Mediterranean fever (recurrent hereditary polyserositis). A six\u2010year study","volume":"75","author":"Majeed HA","year":"1990","journal-title":"Q J Med"}],"container-title":["The Journal of Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2F1346-8138.12929","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/1346-8138.12929","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,24]],"date-time":"2023-09-24T06:27:02Z","timestamp":1695536822000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/1346-8138.12929"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,5,11]]},"references-count":14,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2015,9]]}},"alternative-id":["10.1111\/1346-8138.12929"],"URL":"https:\/\/doi.org\/10.1111\/1346-8138.12929","archive":["Portico"],"relation":{},"ISSN":["0385-2407","1346-8138"],"issn-type":[{"value":"0385-2407","type":"print"},{"value":"1346-8138","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015,5,11]]}}}