{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,27]],"date-time":"2025-09-27T11:40:08Z","timestamp":1758973208550,"version":"3.44.0"},"reference-count":28,"publisher":"Elsevier BV","issue":"8-9","license":[{"start":{"date-parts":[[2018,8,1]],"date-time":"2018-08-01T00:00:00Z","timestamp":1533081600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2018,8,1]],"date-time":"2018-08-01T00:00:00Z","timestamp":1533081600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Annales de Dermatologie et de V\u00e9n\u00e9r\u00e9ologie"],"published-print":{"date-parts":[[2018,8]]},"DOI":"10.1016\/j.annder.2017.11.016","type":"journal-article","created":{"date-parts":[[2018,5,24]],"date-time":"2018-05-24T20:06:25Z","timestamp":1527192385000},"page":"500-504","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"title":["\u00c9tat scl\u00e9reux r\u00e9v\u00e9lant une porphyrie cutan\u00e9e tardive"],"prefix":"10.1016","volume":"145","author":[{"given":"A.","family":"Brunet","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Hainaut","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.annder.2017.11.016_bib0145","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1111\/j.1440-0960.1983.tb00266.x","article-title":"Porphyria and scleroderma: a clinical and laboratory review of 12\u00a0patients","volume":"24","author":"Doyle","year":"1983","journal-title":"Australas J Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0150","doi-asserted-by":"crossref","first-page":"272","DOI":"10.1007\/s00105-014-2783-6","article-title":"[Porphyria cutanea tarda with sclerodermatous changes and hemochromatosis]","volume":"65","author":"Wallaeys","year":"2014","journal-title":"Hautarzt"},{"key":"10.1016\/j.annder.2017.11.016_bib0155","doi-asserted-by":"crossref","first-page":"S117","DOI":"10.1016\/S0923-1811(98)83696-7","article-title":"Morphological investigation of desquamated corneocytes from sensitive skin panels","volume":"16","author":"Yanagi","year":"1998","journal-title":"J Dermatol Sci"},{"key":"10.1016\/j.annder.2017.11.016_bib0160","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1016\/0002-9343(79)90403-0","article-title":"Porphyria cutanea tarda. Clinical features and laboratory findings in 40\u00a0patients","volume":"67","author":"Grossman","year":"1979","journal-title":"Am J Med"},{"key":"10.1016\/j.annder.2017.11.016_bib0165","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1097\/MD.0b013e3181d50928","article-title":"Familial and sporadic porphyria cutanea tarda: clinical and biochemical features and risk factors in 152\u00a0patients","volume":"89","author":"Mu\u00f1oz-Santos","year":"2010","journal-title":"Medicine (Baltimore)"},{"key":"10.1016\/j.annder.2017.11.016_bib0170","doi-asserted-by":"crossref","first-page":"205","DOI":"10.2169\/internalmedicine.49.2888","article-title":"A sclerodermiform porphyria cutanea tarda","volume":"49","author":"Amezyane","year":"2010","journal-title":"Intern Med"},{"key":"10.1016\/j.annder.2017.11.016_bib0175","doi-asserted-by":"crossref","first-page":"422","DOI":"10.1111\/j.1365-2230.2007.02579.x","article-title":"Sclerodermatous changes of face, neck and scalp associated with familial porphyria cutanea tarda","volume":"33","author":"Thomas","year":"2008","journal-title":"Clin Exp Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0180","doi-asserted-by":"crossref","first-page":"589","DOI":"10.1016\/j.annder.2013.04.092","article-title":"L\u00e9sions scl\u00e9rodermiformes dans la porphyrie cutan\u00e9e tardive\u00a0: six observations","volume":"140","author":"Khayat","year":"2013","journal-title":"Ann Dermatol Venereol"},{"key":"10.1016\/j.annder.2017.11.016_bib0185","doi-asserted-by":"crossref","first-page":"1317","DOI":"10.1001\/archderm.148.11.1317-b","article-title":"Progressive sclerotic skin lesions in a 49-year-old man","volume":"148","author":"Cohen","year":"2012","journal-title":"Arch Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0190","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1111\/j.1365-2133.1993.tb03176.x","article-title":"Generalized morphoea secondary to porphyria cutanea tarda","volume":"129","author":"Stevens","year":"1993","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0195","first-page":"203","article-title":"Porphyria cutanea tarda presenting as scleroderma","volume":"85","author":"Zemtsov","year":"2010","journal-title":"Cutis"},{"key":"10.1016\/j.annder.2017.11.016_bib0200","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1111\/j.1365-2230.1990.tb02091.x","article-title":"Porphyria cutanea tarda and scleroderma \u2013\u00a0chance association or related disease: a case report","volume":"15","author":"Sigal-Nahum","year":"1990","journal-title":"Clin Exp Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0205","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1016\/j.autrev.2007.12.004","article-title":"Scleroderma-like disorders","volume":"7","author":"Foti","year":"2008","journal-title":"Autoimmun Rev"},{"key":"10.1016\/j.annder.2017.11.016_bib0210","doi-asserted-by":"crossref","first-page":"1124","DOI":"10.1111\/j.1468-3083.2006.02111.x","article-title":"Laminaria ochroleuca extract reduces skin inflammation","volume":"21","author":"Bonneville","year":"2007","journal-title":"J Eur Acad Dermatol Venereol"},{"key":"10.1016\/j.annder.2017.11.016_bib0215","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1016\/j.bpg.2010.07.002","article-title":"Porphyria cutanea tarda \u2013\u00a0When skin meets liver","volume":"24","author":"Frank","year":"2010","journal-title":"Best Pract Res Clin Gastroenterol"},{"key":"10.1016\/j.annder.2017.11.016_bib0220","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1172\/JCI110423","article-title":"stimulation of collagen biosynthesis in human skin fibroblasts. A unique dark effect of porphyrin","volume":"69","author":"Varigos","year":"1982","journal-title":"J Clin Invest"},{"issue":"Suppl 2","key":"10.1016\/j.annder.2017.11.016_bib0225","doi-asserted-by":"crossref","first-page":"S75","DOI":"10.33549\/physiolres.930000.55.S2.75","article-title":"Hemochromatosis gene sequence deviations in German patients with porphyria cutanea tarda","volume":"55","author":"Frank","year":"2006","journal-title":"Physiol Res"},{"key":"10.1016\/j.annder.2017.11.016_bib0230","doi-asserted-by":"crossref","first-page":"530","DOI":"10.1590\/abd1806-4841.20132048","article-title":"Precipitating factors of porphyria cutanea tarda in Brazil with emphasis on hemochromatosis gene (HFE) mutations. Study of 60\u00a0patients","volume":"88","author":"Vieira","year":"2013","journal-title":"An Bras Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0235","doi-asserted-by":"crossref","first-page":"868","DOI":"10.1046\/j.1523-1747.2000.00148.x","article-title":"Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tarda","volume":"115","author":"Brady","year":"2000","journal-title":"J Invest Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0240","doi-asserted-by":"crossref","first-page":"564","DOI":"10.1016\/S0168-8278(96)80141-3","article-title":"Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overload","volume":"24","author":"Fargion","year":"1996","journal-title":"J Hepatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0245","doi-asserted-by":"crossref","first-page":"533","DOI":"10.1046\/j.1365-2133.2001.04079.x","article-title":"HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36\u00a0cases from southern France","volume":"144","author":"Dereure","year":"2001","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0250","first-page":"600","article-title":"R\u00f4le du g\u00e8ne de l\u2019h\u00e9mochromatose (HFE) dans la porphyrie cutan\u00e9e tardive","volume":"128","author":"Skowron","year":"2001","journal-title":"Ann Dermatol Venereol"},{"key":"10.1016\/j.annder.2017.11.016_bib0255","doi-asserted-by":"crossref","first-page":"1565","DOI":"10.1182\/blood.V95.5.1565.005k42_1565_1571","article-title":"Hemochromatosis genes and other factors contributing to the pathogenesis of porphyria cutanea tarda","volume":"95","author":"Bulaj","year":"2000","journal-title":"Blood"},{"key":"10.1016\/j.annder.2017.11.016_bib0260","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1006\/bcmd.1997.0143","article-title":"Compound heterozygotes for hemochromatosis gene mutations: may they help to understand the pathophysiology of the disease?","volume":"23","author":"Aguilar Martinez","year":"1997","journal-title":"Blood Cells Mol Dis"},{"key":"10.1016\/j.annder.2017.11.016_bib0265","first-page":"918","article-title":"Activation of uroporphyrinogen decarboxylase by ferrous iron in porphyria cutanea tarda","volume":"56","author":"Blekkenhorst","year":"1979","journal-title":"South Afr Med J"},{"key":"10.1016\/j.annder.2017.11.016_bib0270","doi-asserted-by":"crossref","first-page":"1116","DOI":"10.1046\/j.1365-2133.2000.03874.x","article-title":"Iron overload in porphyria cutanea tarda","volume":"143","author":"Bygum","year":"2000","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.annder.2017.11.016_bib0275","first-page":"37","article-title":"Iron storage in porphyria cutanea tarda","volume":"188","author":"Lundvall","year":"1970","journal-title":"J Intern Med"},{"key":"10.1016\/j.annder.2017.11.016_bib0140","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1016\/j.jaad.2003.08.015","article-title":"Association of porphyria cutanea tarda with hereditary hemochromatosis","volume":"51","author":"Mehrany","year":"2004","journal-title":"J Am Acad Dermatol"}],"container-title":["Annales de Dermatologie et de V\u00e9n\u00e9r\u00e9ologie"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0151963818303892?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0151963818303892?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,27]],"date-time":"2025-09-27T11:06:13Z","timestamp":1758971173000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0151963818303892"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,8]]},"references-count":28,"journal-issue":{"issue":"8-9","published-print":{"date-parts":[[2018,8]]}},"alternative-id":["S0151963818303892"],"URL":"https:\/\/doi.org\/10.1016\/j.annder.2017.11.016","relation":{},"ISSN":["0151-9638"],"issn-type":[{"type":"print","value":"0151-9638"}],"subject":[],"published":{"date-parts":[[2018,8]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"\u00c9tat scl\u00e9reux r\u00e9v\u00e9lant une porphyrie cutan\u00e9e tardive","name":"articletitle","label":"Article Title"},{"value":"Annales de Dermatologie et de V\u00e9n\u00e9r\u00e9ologie","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.annder.2017.11.016","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}