{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T05:54:24Z","timestamp":1791957264646,"version":"4.3.4"},"reference-count":132,"publisher":"Elsevier BV","issue":"9","license":[{"start":{"date-parts":[[2019,11,1]],"date-time":"2019-11-01T00:00:00Z","timestamp":1572566400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,11,1]],"date-time":"2019-11-01T00:00:00Z","timestamp":1572566400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.es","elsevier.es","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Actas Dermo-Sifiliogr\u00e1ficas"],"published-print":{"date-parts":[[2019,11]]},"DOI":"10.1016\/j.ad.2019.02.012","type":"journal-article","created":{"date-parts":[[2019,6,4]],"date-time":"2019-06-04T01:50:10Z","timestamp":1559613010000},"page":"710-727","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["La biopsia cut\u00e1nea en el contexto de la enfermedad sist\u00e9mica"],"prefix":"10.1016","volume":"110","author":[{"given":"A.","family":"Fernandez-Flores","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.ad.2019.02.012_bib0695","doi-asserted-by":"crossref","first-page":"520","DOI":"10.1016\/j.clindermatol.2015.05.002","article-title":"Cutaneous manifestations of systemic autoinflammatory disorders","volume":"33","author":"B\u00f6l\u00fckbasi","year":"2015","journal-title":"Clin Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0700","doi-asserted-by":"crossref","first-page":"614","DOI":"10.1097\/DAD.0000000000000288","article-title":"Interstitial granulomatous dermatitis: A clinicopathological study","volume":"37","author":"Coutinho","year":"2015","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0705","doi-asserted-by":"crossref","first-page":"482","DOI":"10.1111\/bjd.14364","article-title":"Hidradenitis suppurativa, neutrophilic dermatoses and autoinflammation: What's the link?","volume":"174","author":"Marzano","year":"2016","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0710","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1016\/j.jaad.2010.12.025","article-title":"Pyoderma gangrenosum, acne, and suppurative hidradenitis (PASH) \u2014 A new autoinflammatory syndrome distinct from PAPA syndrome","volume":"66","author":"Braun-Falco","year":"2012","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0715","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1111\/cup.13096","article-title":"Lymphocytes in Sweet syndrome: A potential diagnostic pitfall","volume":"45","author":"Kazlouskaya","year":"2018","journal-title":"J Cutan Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0720","doi-asserted-by":"crossref","first-page":"526","DOI":"10.1111\/j.1600-0560.2006.00654.x","article-title":"Clonality in the setting of Sweet's syndrome and pyoderma gangrenosum is not limited to underlying myeloproliferative disease","volume":"34","author":"Magro","year":"2007","journal-title":"J Cutan Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0725","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1097\/MD.0000000000000021","article-title":"Adult-onset still disease: Manifestations, treatment, outcome, and prognostic factors in 57 patients","volume":"93","author":"Gerfaud-Valentin","year":"2014","journal-title":"Medicine (Baltimore)."},{"key":"10.1016\/j.ad.2019.02.012_bib0730","doi-asserted-by":"crossref","first-page":"144","DOI":"10.1016\/j.semarthrit.2006.07.001","article-title":"Pathogenesis and management of adult-onset Still's disease","volume":"36","author":"Efthimiou","year":"2006","journal-title":"Semin Arthritis Rheum."},{"key":"10.1016\/j.ad.2019.02.012_bib0735","doi-asserted-by":"crossref","first-page":"e6318","DOI":"10.1097\/MD.0000000000006318","article-title":"Adult-onset Still's disease with atypical cutaneous manifestations","volume":"96","author":"Narv\u00e1ez Garcia","year":"2017","journal-title":"Medicine (Baltimore)."},{"key":"10.1016\/j.ad.2019.02.012_bib0740","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1111\/1346-8138.12426","article-title":"Persistent pruritic papules and plaques associated with adult-onset Still's disease: Report of six cases","volume":"41","author":"Kikuchi","year":"2014","journal-title":"J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0745","doi-asserted-by":"crossref","first-page":"710","DOI":"10.1046\/j.1365-2133.1999.03115.x","article-title":"Adult-onset Still's disease with persistent plaques","volume":"141","author":"L\u00fcbbe","year":"1999","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0750","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1159\/000247150","article-title":"Persistent dermal plaque lesions in adult onset Still's disease","volume":"188","author":"Kaur","year":"1994","journal-title":"Dermatology."},{"key":"10.1016\/j.ad.2019.02.012_bib0755","doi-asserted-by":"crossref","first-page":"e154","DOI":"10.1111\/ijd.12608","article-title":"Atypical eruption but still Still's: Case report and review of the literature","volume":"54","author":"Kavusi","year":"2015","journal-title":"Int J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0760","doi-asserted-by":"crossref","first-page":"793","DOI":"10.1111\/cup.13320","article-title":"An atypical persistent eruption of Adult-onset Still's disease with neutrophilic urticarial dermatosis-like dermal features: A case report and review of the literature","volume":"45","author":"Nassereddine","year":"2018","journal-title":"J Cutan Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0765","doi-asserted-by":"crossref","first-page":"906","DOI":"10.1046\/j.1365-2133.1998.02237.x","article-title":"Urticaria as a presentation of adult Still's disease","volume":"138","author":"Setterfield","year":"1998","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0770","doi-asserted-by":"crossref","first-page":"102","DOI":"10.2340\/00015555-1615","article-title":"Prurigo pigmentosa-like persistent papules and plaques in a patient with adult-onset Still's disease","volume":"94","author":"Cho","year":"2014","journal-title":"Acta Derm Venereol."},{"key":"10.1016\/j.ad.2019.02.012_bib0775","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1016\/j.jdcr.2017.12.009","article-title":"Atypical Still disease with necrotic keratinocytes: A histologic mimicker of erythema multiforme","volume":"4","author":"Khanna","year":"2018","journal-title":"JAAD Case Rep."},{"key":"10.1016\/j.ad.2019.02.012_bib0780","doi-asserted-by":"crossref","first-page":"1003","DOI":"10.1016\/j.jaad.2005.02.032","article-title":"Histopathology of persistent papules and plaques in adult-onset Still's disease","volume":"52","author":"Lee","year":"2005","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0785","doi-asserted-by":"crossref","first-page":"294","DOI":"10.1016\/j.jaad.2015.04.063","article-title":"Updates in adult-onset Still disease: Atypical cutaneous manifestations and associations with delayed malignancy","volume":"73","author":"Sun","year":"2015","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0790","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1097\/DAD.0b013e3180332826","article-title":"Unique histopathologic findings in a patient with adult-onset Still disease","volume":"29","author":"Wolgamot","year":"2007","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0795","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1590\/abd1806-4841.20186836","article-title":"Oral mucosa lesions as atypical manifestation of adult-onset Still's disease","volume":"93","author":"Brance","year":"2018","journal-title":"An Bras Dermatol."},{"issue":"4 Suppl 98","key":"10.1016\/j.ad.2019.02.012_bib0800","first-page":"66","article-title":"IgG4-related disease: Pathophysiologic insights drive emerging treatment approaches","volume":"34","author":"Stone","year":"2016","journal-title":"Clin Exp Rheumatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0805","doi-asserted-by":"crossref","first-page":"473","DOI":"10.1007\/s11926-011-0213-7","article-title":"The clinical and pathological features of IgG(4)-related disease","volume":"13","author":"Khosroshahi","year":"2011","journal-title":"Curr Rheumatol Rep."},{"key":"10.1016\/j.ad.2019.02.012_bib0810","first-page":"217","article-title":"IgG4-related disease","volume":"16","author":"Umehara","year":"2015","journal-title":"JOP"},{"key":"10.1016\/j.ad.2019.02.012_bib0815","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1136\/jcp.2010.085613","article-title":"Numerous IgG4-positive plasma cells are ubiquitous in diverse localised non-specific chronic inflammatory conditions and need to be distinguished from IgG4-related systemic disorders","volume":"64","author":"Strehl","year":"2011","journal-title":"J Clin Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0820","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1007\/s00251-006-0178-2","article-title":"Two critical genes (HLA-DRB1 and ABCF1)in the HLA region are associated with the susceptibility to autoimmune pancreatitis","volume":"59","author":"Ota","year":"2007","journal-title":"Immunogenetics."},{"key":"10.1016\/j.ad.2019.02.012_bib0825","doi-asserted-by":"crossref","first-page":"573","DOI":"10.1016\/S0016-5085(00)70264-2","article-title":"Autoimmune-related pancreatitis is associated with autoantibodies and a Th1\/Th2-type cellular immune response","volume":"118","author":"Okazaki","year":"2000","journal-title":"Gastroenterology."},{"key":"10.1016\/j.ad.2019.02.012_bib0830","doi-asserted-by":"crossref","first-page":"1538","DOI":"10.1002\/hep.21697","article-title":"Th2 and regulatory immune reactions are increased in immunoglobin G4-related sclerosing pancreatitis and cholangitis","volume":"45","author":"Zen","year":"2007","journal-title":"Hepatology."},{"key":"10.1016\/j.ad.2019.02.012_bib0835","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1146\/annurev.immunol.26.021607.090344","article-title":"T follicular helper (TFH) cells in normal and dysregulated immune responses","volume":"26","author":"King","year":"2008","journal-title":"Annu Rev Immunol."},{"key":"10.1016\/j.ad.2019.02.012_bib0840","doi-asserted-by":"crossref","first-page":"59","DOI":"10.3409\/fb64_2.59","article-title":"Prediction of developmentally competent chromatin conformation in mouse antral oocytes","volume":"64","author":"Daszkiewicz","year":"2016","journal-title":"Folia Biol (Krakow)."},{"key":"10.1016\/j.ad.2019.02.012_bib0845","doi-asserted-by":"crossref","first-page":"580814","DOI":"10.1155\/2012\/580814","article-title":"Cutoff values of serum IgG4 and histopathological IgG4+ plasma cells for diagnosis of patients with IgG4-related disease","volume":"2012","author":"Masaki","year":"2012","journal-title":"Int J Rheumatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0850","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1016\/j.jaad.2016.01.046","article-title":"Cutaneous manifestations of IgG4-related disease (RD): A systematic review","volume":"75","author":"Charrow","year":"2016","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0855","doi-asserted-by":"crossref","first-page":"1314","DOI":"10.1001\/archderm.1986.01660230106022","article-title":"Systemic plasmacytosis. A syndrome of peculiar multiple skin eruptions, generalized lymphadenopathy, and polyclonal hypergammaglobulinemia","volume":"122","author":"Watanabe","year":"1986","journal-title":"Arch Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0860","doi-asserted-by":"crossref","first-page":"959","DOI":"10.1111\/bjd.13296","article-title":"IgG4-related skin disease","volume":"171","author":"Tokura","year":"2014","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0865","doi-asserted-by":"crossref","first-page":"1269","DOI":"10.1016\/j.humpath.2009.01.013","article-title":"High ratio of IgG4-positive plasma cell infiltration in cutaneous plasmacytosis \u2014 Is this a cutaneous manifestation of IgG4-related disease?","volume":"40","author":"Miyagawa-Hayashino","year":"2009","journal-title":"Hum Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0870","doi-asserted-by":"crossref","first-page":"255","DOI":"10.1684\/ejd.2013.1962","article-title":"IgG4-positive cells in skin lesions of cutaneous and systemic plasmacytosis","volume":"23","author":"Kato","year":"2013","journal-title":"Eur J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0875","doi-asserted-by":"crossref","first-page":"1095","DOI":"10.1007\/s00277-018-3272-2","article-title":"Adult T cell leukemia\/lymphoma with different pathological features in each tumor site","volume":"97","author":"Nakayama","year":"2018","journal-title":"Ann Hematol."},{"key":"10.1016\/j.ad.2019.02.012_bib0880","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1111\/j.1365-2133.2009.09401.x","article-title":"Lupus erythematosus tumidus is a separate subtype of cutaneous lupus erythematosus","volume":"162","author":"Schmitt","year":"2010","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0885","doi-asserted-by":"crossref","first-page":"e0375","DOI":"10.1097\/MD.0000000000010375","article-title":"A case report of lupus erythematosus tumidus converted from discoid lupus erythematosus","volume":"97","author":"Chen","year":"2018","journal-title":"Medicine (Baltimore)."},{"key":"10.1016\/j.ad.2019.02.012_bib0890","series-title":"Histologic Diagnosis of Inflammatory Skin Diseases","first-page":"170","article-title":"Inflammatory diseases","author":"Ackerman","year":"1997"},{"key":"10.1016\/j.ad.2019.02.012_bib0895","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.jaut.2018.07.007","article-title":"A comprehensive review of immune-mediated dermatopathology in systemic lupus erythematosus","volume":"93","author":"Li","year":"2018","journal-title":"J Autoimmun."},{"key":"10.1016\/j.ad.2019.02.012_bib0900","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1136\/mp.50.1.9","article-title":"Intracellular staining of Mx proteins in cells from peripheral blood, bone marrow and skin","volume":"50","author":"Al-Masri","year":"1997","journal-title":"Mol Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0905","doi-asserted-by":"crossref","first-page":"958","DOI":"10.1046\/j.1365-2133.2001.04182.x","article-title":"Apoptosis in different cutaneous manifestations of lupus erythematosus","volume":"144","author":"Baima","year":"2001","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0910","doi-asserted-by":"crossref","first-page":"794","DOI":"10.1177\/0961203307081895","article-title":"Translocation of the novel cytokine HMGB1 to the cytoplasm and extracellular space coincides with the peak of clinical activity in experimentally UV-induced lesions of cutaneous lupus erythematosus","volume":"16","author":"Barkauskaite","year":"2007","journal-title":"Lupus."},{"key":"10.1016\/j.ad.2019.02.012_bib0915","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.semarthrit.2017.11.003","article-title":"Clinical, histological, immunological presentations and outcomes of bullous systemic lupus erythematosus: 10 new cases and a literature review of 118 cases","volume":"48","author":"de Risi-Pugliese","year":"2018","journal-title":"Semin Arthritis Rheum."},{"key":"10.1016\/j.ad.2019.02.012_bib0920","doi-asserted-by":"crossref","first-page":"866","DOI":"10.1016\/j.autrev.2018.03.011","article-title":"Classification of primary antiphospholipid syndrome as systemic lupus erythematosus: Analysis of a cohort of 214 patients","volume":"17","author":"Paule","year":"2018","journal-title":"Autoimmun Rev."},{"key":"10.1016\/j.ad.2019.02.012_bib0925","doi-asserted-by":"crossref","first-page":"e0186","DOI":"10.1097\/MD.0000000000010186","article-title":"Hidradenitis suppurativa associated with systemic lupus erythematosus: A case report","volume":"97","author":"Ben David","year":"2018","journal-title":"Medicine (Baltimore)."},{"key":"10.1016\/j.ad.2019.02.012_bib0930","doi-asserted-by":"crossref","first-page":"1152","DOI":"10.1111\/exd.13754","article-title":"Ex vivo fluorescence confocal microscopy for intraoperative, real-time diagnosis of cutaneous inflammatory diseases: A preliminary study","volume":"27","author":"Bertoni","year":"2018","journal-title":"Exp Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0935","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1016\/j.jid.2018.06.185","article-title":"Chronic inflammation promotes skin carcinogenesis in cancer-prone discoid lupus erythematosus","volume":"139","author":"Zaalberg","year":"2019","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib0940","first-page":"35","article-title":"Clinical manifestations of Kikuchi's disease in southern Taiwan","volume":"38","author":"Yu","year":"2005","journal-title":"J Microbiol Immunol Infect."},{"key":"10.1016\/j.ad.2019.02.012_bib0945","first-page":"1791627","article-title":"A challenging case of Kikuchi-Fujimoto disease associated with systemic lupus erythematosus and review of the literature","volume":"2018","author":"G\u0103man","year":"2018","journal-title":"Case Rep Hematol."},{"key":"10.1016\/j.ad.2019.02.012_bib0950","doi-asserted-by":"crossref","first-page":"798","DOI":"10.1097\/00000478-199507000-00008","article-title":"Kikuchi's disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic subtypes, immunohistology, and DNA ploidy","volume":"19","author":"Kuo","year":"1995","journal-title":"Am J Surg Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0955","doi-asserted-by":"crossref","first-page":"613","DOI":"10.1046\/j.1365-2141.1996.d01-1964.x","article-title":"Elevated serum interferon gamma and interleukin-6 in patients with necrotizing lymphadenitis (Kikuchi's disease)","volume":"95","author":"Kubota","year":"1996","journal-title":"Br J Haematol."},{"key":"10.1016\/j.ad.2019.02.012_bib0960","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1007\/BF02981907","article-title":"Elevated serum-soluble Fas ligand in histiocytic necrotizing lymphadenitis","volume":"73","author":"Kato","year":"2001","journal-title":"Int J Hematol."},{"key":"10.1016\/j.ad.2019.02.012_bib0965","doi-asserted-by":"crossref","first-page":"805","DOI":"10.1136\/ard.51.6.805","article-title":"Histiocytic necrotising lymphadenitis in systemic lupus erythematosus","volume":"51","author":"Litwin","year":"1992","journal-title":"Ann Rheum Dis."},{"key":"10.1016\/j.ad.2019.02.012_bib0970","first-page":"163","article-title":"Kikuchi-Fujimoto disease and systemic lupus erythematosus","volume":"9","author":"Baenas","year":"2016","journal-title":"Int Med Case Rep J."},{"key":"10.1016\/j.ad.2019.02.012_bib0975","doi-asserted-by":"crossref","first-page":"900","DOI":"10.1016\/j.semarthrit.2011.11.001","article-title":"Autoimmune manifestations of Kikuchi disease","volume":"41","author":"Sope\u00f1a","year":"2012","journal-title":"Semin Arthritis Rheum."},{"key":"10.1016\/j.ad.2019.02.012_bib0980","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1016\/j.semarthrit.2017.01.011","article-title":"Clinical association between Kikuchi's disease and systemic lupus erythematosus: A systematic literature review","volume":"47","author":"Sope\u00f1a","year":"2017","journal-title":"Semin Arthritis Rheum."},{"key":"10.1016\/j.ad.2019.02.012_bib0985","doi-asserted-by":"crossref","first-page":"1245","DOI":"10.1016\/j.humpath.2010.02.002","article-title":"The cutaneous lesions of Kikuchi's disease: A comprehensive analysis of 16 cases based on the clinicopathologic, immunohistochemical, and immunofluorescence studies with an emphasis on the differential diagnosis","volume":"41","author":"Kim","year":"2010","journal-title":"Hum Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0990","doi-asserted-by":"crossref","first-page":"731","DOI":"10.1093\/ajcp\/90.6.731","article-title":"Hematoxylin-stained bodies and tissue LE cells in a skeletal muscle biopsy","volume":"90","author":"McMullan","year":"1988","journal-title":"Am J Clin Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib0995","doi-asserted-by":"crossref","first-page":"300","DOI":"10.1177\/1093526617734948","article-title":"Hematoxylin bodies in pediatric bone marrow aspirates and their utility in the diagnosis of systemic lupus erythematosus","volume":"21","author":"Xu","year":"2018","journal-title":"Pediatr Dev Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1000","doi-asserted-by":"crossref","first-page":"202","DOI":"10.1097\/PAI.0b013e318074c94c","article-title":"The histiocytic component of cutaneous manifestations of Kikuchi disease expresses myeloperoxidase","volume":"16","author":"Fernandez-Flores","year":"2008","journal-title":"Appl Immunohistochem Mol Morphol."},{"key":"10.1016\/j.ad.2019.02.012_bib1005","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1016\/j.jaad.2008.03.012","article-title":"Kikuchi's disease: Case report and systematic review of cutaneous and histopathologic presentations","volume":"59","author":"Atwater","year":"2008","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1010","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1177\/0961203309345793","article-title":"Necrotizing lymphadenitis: Kikuchi-Fujimoto disease alias lupus lymphadenitis?","volume":"19","author":"Cramer","year":"2010","journal-title":"Lupus."},{"key":"10.1016\/j.ad.2019.02.012_bib1015","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1016\/S0049-0172(96)80028-X","article-title":"Necrotizing lymphadenitis associated with systemic lupus erythematosus","volume":"26","author":"Eisner","year":"1996","journal-title":"Semin Arthritis Rheum."},{"key":"10.1016\/j.ad.2019.02.012_bib1020","doi-asserted-by":"crossref","DOI":"10.3390\/nu10050602","article-title":"Dermatitis herpetiformis: A common extraintestinal manifestation of coeliac disease","volume":"10","author":"Reunala","year":"2018","journal-title":"Nutrients."},{"key":"10.1016\/j.ad.2019.02.012_bib1025","first-page":"4","article-title":"Gluten intolerance and skin diseases","volume":"16","author":"Humbert","year":"2006","journal-title":"Eur J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1030","doi-asserted-by":"crossref","first-page":"1199","DOI":"10.1016\/j.jaci.2004.03.012","article-title":"Allergy prevalence in adult celiac disease","volume":"113","author":"Ciacci","year":"2004","journal-title":"J Allergy Clin Immunol."},{"key":"10.1016\/j.ad.2019.02.012_bib1035","doi-asserted-by":"crossref","first-page":"681","DOI":"10.1684\/ejd.2013.2158","article-title":"Does urticaria risk increase in patients with celiac disease? A large population-based cohort study","volume":"23","author":"Ludvigsson","year":"2013","journal-title":"Eur J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1040","doi-asserted-by":"crossref","first-page":"2010","DOI":"10.1038\/jid.2011.162","article-title":"Psoriasis in a nationwide cohort study of patients with celiac disease","volume":"131","author":"Ludvigsson","year":"2011","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1045","doi-asserted-by":"crossref","first-page":"e329","DOI":"10.1111\/bjd.15684","article-title":"The association between psoriasis and coeliac disease","volume":"177","author":"Egeberg","year":"2017","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1050","doi-asserted-by":"crossref","first-page":"41","DOI":"10.4103\/0019-5154.198031","article-title":"Psoriasis and risk of celiac disease: A systematic review and meta-analysis","volume":"62","author":"Ungprasert","year":"2017","journal-title":"Indian J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1055","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1016\/j.jaad.2014.03.017","article-title":"Diet and psoriasis, part II: Celiac disease and role of a gluten-free diet","volume":"71","author":"Bhatia","year":"2014","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1060","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.jdent.2017.07.001","article-title":"Enamel defects and aphthous stomatitis in celiac and healthy subjects: Systematic review and meta-analysis of controlled studies","volume":"65","author":"Nieri","year":"2017","journal-title":"J Dent."},{"key":"10.1016\/j.ad.2019.02.012_bib1065","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1111\/bjd.14930","article-title":"Rosacea and gastrointestinal disorders: A population-based cohort study","volume":"176","author":"Egeberg","year":"2017","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1070","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1093\/ecco-jcc\/jjx178","article-title":"Cutaneous morbidity among inflammatory bowel disease patients: A cohort study","volume":"12","author":"Vide","year":"2018","journal-title":"J Crohns Colitis."},{"key":"10.1016\/j.ad.2019.02.012_bib1075","first-page":"225","article-title":"Dermatologic manifestations of inflammatory bowel disease: A review","volume":"25","author":"Keyal","year":"2018","journal-title":"Discov Med."},{"key":"10.1016\/j.ad.2019.02.012_bib1080","first-page":"E16","article-title":"Metastatic vulvovaginal Crohn disease in the setting of well-controlled intestinal disease","volume":"102","author":"Woody","year":"2018","journal-title":"Cutis."},{"key":"10.1016\/j.ad.2019.02.012_bib1085","doi-asserted-by":"crossref","first-page":"580","DOI":"10.1136\/pgmj.2004.031633","article-title":"Important cutaneous manifestations of inflammatory bowel disease","volume":"81","author":"Trost","year":"2005","journal-title":"Postgrad Med J."},{"key":"10.1016\/j.ad.2019.02.012_bib1090","doi-asserted-by":"crossref","first-page":"394","DOI":"10.1007\/s12016-017-8649-9","article-title":"Skin manifestations associated with autoimmune liver diseases: A systematic review","volume":"53","author":"Terziroli Beretta-Piccoli","year":"2017","journal-title":"Clin Rev Allergy Immunol."},{"key":"10.1016\/j.ad.2019.02.012_bib1095","doi-asserted-by":"crossref","first-page":"e0004","DOI":"10.1097\/MD.0000000000010004","article-title":"Primary cutaneous amyloidosis associated with autoimmune hepatitis-primary biliary cirrhosis overlap syndrome and Sj\u00f6gren syndrome: A case report","volume":"97","author":"Yan","year":"2018","journal-title":"Medicine (Baltimore)."},{"key":"10.1016\/j.ad.2019.02.012_bib1100","doi-asserted-by":"crossref","first-page":"1334","DOI":"10.1016\/j.jhep.2017.08.011","article-title":"Hepatitis E virus-induced primary cutaneous CD30(+) T cell lymphoproliferative disorder","volume":"67","author":"Mallet","year":"2017","journal-title":"J Hepatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1105","doi-asserted-by":"crossref","first-page":"e129","DOI":"10.1111\/jdv.15330","article-title":"Subacute cutaneous lupus erythematosus triggered by an antiviral treatment combination for hepatitis C virus infection","volume":"33","author":"Prenner","year":"2019","journal-title":"J Eur Acad Dermatol Venereol."},{"key":"10.1016\/j.ad.2019.02.012_bib1110","first-page":"CD011403","article-title":"Treatment for hepatitis C virus-associated mixed cryoglobulinaemia","volume":"5","author":"Montero","year":"2018","journal-title":"Cochrane Database Syst Rev."},{"key":"10.1016\/j.ad.2019.02.012_bib1115","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1097\/DAD.0b013e31823465c7","article-title":"Cutaneous amyloidosis: A concept review","volume":"34","author":"Fernandez-Flores","year":"2012","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1120","doi-asserted-by":"crossref","first-page":"20","DOI":"10.4103\/idoj.IDOJ_160_17","article-title":"Mucocutaneous manifestations in patients with chronic kidney disease: A cross-sectional study","volume":"9","author":"Rashpa","year":"2018","journal-title":"Indian Dermatol Online J."},{"key":"10.1016\/j.ad.2019.02.012_bib1125","doi-asserted-by":"crossref","first-page":"859","DOI":"10.1111\/cup.12396","article-title":"Fumarate hydratase immunohistochemical staining may help to identify patients with multiple cutaneous and uterine leiomyomatosis (MCUL) and hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome","volume":"41","author":"Llamas-Velasco","year":"2014","journal-title":"J Cutan Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1130","doi-asserted-by":"crossref","first-page":"697","DOI":"10.1111\/j.1346-8138.2011.01206.x","article-title":"Cutaneous silica granuloma with generalized involvement of lymph nodes","volume":"38","author":"Hou","year":"2011","journal-title":"J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1135","doi-asserted-by":"crossref","first-page":"198","DOI":"10.1111\/jdv.15167","article-title":"Physicochemical characterization of inorganic deposits associated with granulomas in cutaneous sarcoidosis","volume":"33","author":"Colboc","year":"2019","journal-title":"J Eur Acad Dermatol Venereol."},{"key":"10.1016\/j.ad.2019.02.012_bib1140","doi-asserted-by":"crossref","first-page":"692","DOI":"10.1001\/archderm.1991.01680040100011","article-title":"Cutaneous silica granuloma. A rare entity or rarely diagnosed? Report of two cases with review of the literature","volume":"127","author":"Mowry","year":"1991","journal-title":"Arch Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1145","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1097\/00000372-199306000-00002","article-title":"Cutaneous sarcoidosis and foreign bodies","volume":"15","author":"Walsh","year":"1993","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1150","doi-asserted-by":"crossref","first-page":"408","DOI":"10.1097\/00000372-200010000-00004","article-title":"Foreign bodies in sarcoidosis","volume":"22","author":"Kim","year":"2000","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1155","first-page":"405","article-title":"Foreign-body granulomas and sarcoidosis; a clinical and histo-pathological study","volume":"108","author":"Lofgren","year":"1955","journal-title":"Acta Chir Scand."},{"key":"10.1016\/j.ad.2019.02.012_bib1160","first-page":"427","article-title":"Foreign bodies in granulomatous cutaneous lesions of patients with systemic sarcoidosis","volume":"137","author":"Marcoval","year":"2001","journal-title":"Arch Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1165","first-page":"69","article-title":"Silicon granuloma of skin and subcutaneous tissue","volume":"Suppl 248","author":"Eskeland","year":"1974","journal-title":"Acta Pathol Microbiol Scand Suppl."},{"key":"10.1016\/j.ad.2019.02.012_bib1170","first-page":"328","article-title":"Birefringent particles in granulomatous dermatitis, sarcoidal-type, as well as in other non-granulomatous skin disorders in patients without sarcoidosis","volume":"110","author":"Fernandez-Flores","year":"2009","journal-title":"Bratisl Med J \/ Bratisl Lek Listy."},{"key":"10.1016\/j.ad.2019.02.012_bib1175","first-page":"321","article-title":"Does cutaneous silica granuloma develop mainly in predisposed patients?","volume":"16","author":"Fernandez-Flores","year":"2006","journal-title":"Eur J Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1180","first-page":"900","article-title":"Sarcoidal granulomas in a cosmetic tattoo in association with pulmonary sarcoidosis","volume":"8","author":"Baumgartner","year":"2010","journal-title":"J Dtsch Dermatol Ges."},{"key":"10.1016\/j.ad.2019.02.012_bib1185","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1111\/j.1524-4725.2008.01053.x","article-title":"Cutaneous granulomatous reaction from mesotherapy","volume":"35","author":"Gokdemir","year":"2009","journal-title":"Dermatol Surg."},{"issue":"2 Suppl","key":"10.1016\/j.ad.2019.02.012_bib1190","doi-asserted-by":"crossref","first-page":"S54","DOI":"10.1016\/j.jaad.2006.05.055","article-title":"Silica granuloma induced by indwelling catheter","volume":"57","author":"Kenmochi","year":"2007","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1195","doi-asserted-by":"crossref","first-page":"362","DOI":"10.1097\/DAD.0000000000000928","article-title":"Specific skin lesions of sarcoidosis located at venipuncture points for blood sample collection","volume":"40","author":"Marcoval","year":"2018","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1200","doi-asserted-by":"crossref","first-page":"e11","DOI":"10.1164\/rccm.201104-0640IM","article-title":"Diffuse talc granulomatosis in a patient with Crohn's disease","volume":"186","author":"Weiner","year":"2012","journal-title":"Am J Respir Crit Care Med."},{"key":"10.1016\/j.ad.2019.02.012_bib1205","doi-asserted-by":"crossref","first-page":"1607","DOI":"10.1093\/jnci\/djt277","article-title":"Cowden syndrome and the PTEN hamartoma tumor syndrome: Systematic review and revised diagnostic criteria","volume":"105","author":"Pilarski","year":"2013","journal-title":"J Natl Cancer Inst."},{"key":"10.1016\/j.ad.2019.02.012_bib1210","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1016\/j.oooo.2018.08.016","article-title":"Variable expressivity and novel PTEN mutations in Cowden syndrome","volume":"127","author":"Machado","year":"2019","journal-title":"Oral Surg Oral Med Oral Pathol Oral Radiol."},{"key":"10.1016\/j.ad.2019.02.012_bib1215","doi-asserted-by":"crossref","first-page":"97","DOI":"10.2169\/internalmedicine.9052-17","article-title":"Cowden syndrome with a novel PTEN mutation presenting with partial epilepsy related to focal cortical dysplasia","volume":"57","author":"Adachi","year":"2018","journal-title":"Intern Med."},{"key":"10.1016\/j.ad.2019.02.012_bib1220","doi-asserted-by":"crossref","first-page":"512","DOI":"10.4103\/2229-5178.193911","article-title":"Mucocutaneous manifestations of Cowden's syndrome","volume":"7","author":"Reddy","year":"2016","journal-title":"Indian Dermatol Online J."},{"key":"10.1016\/j.ad.2019.02.012_bib1225","doi-asserted-by":"crossref","first-page":"306","DOI":"10.5021\/ad.2015.27.3.306","article-title":"Cowden syndrome with a novel germline PTEN mutation and an unusual clinical course","volume":"27","author":"Seol","year":"2015","journal-title":"Ann Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1230","doi-asserted-by":"crossref","first-page":"493","DOI":"10.1111\/j.1600-0560.2012.01888.x","article-title":"Trichilemmomas show loss of PTEN in Cowden syndrome but only rarely in sporadic tumors","volume":"39","author":"Al-Zaid","year":"2012","journal-title":"J Cutan Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1235","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1097\/DAD.0b013e31827e28f7","article-title":"Phosphatase and tensin homolog immunohistochemical staining and clinical criteria for Cowden syndrome in patients with trichilemmoma or associated lesions","volume":"35","author":"Jin","year":"2013","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1240","doi-asserted-by":"crossref","first-page":"e1007352","DOI":"10.1371\/journal.pgen.1007352","article-title":"Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations","volume":"14","author":"Yehia","year":"2018","journal-title":"PLoS Genet."},{"key":"10.1016\/j.ad.2019.02.012_bib1245","doi-asserted-by":"crossref","first-page":"e253","DOI":"10.1111\/pde.13535","article-title":"Segmental storiform collagenomas: Expanding the spectrum of PTEN hamartoma tumor syndrome in children","volume":"35","author":"Habeshian","year":"2018","journal-title":"Pediatr Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1250","first-page":"32","article-title":"Hereditary nonpolyposis colorectal cancer (HNPCC)\/Lynch syndrome","volume":"110","author":"Steinke","year":"2013","journal-title":"Dtsch Arztebl Int."},{"key":"10.1016\/j.ad.2019.02.012_bib1255","doi-asserted-by":"crossref","first-page":"479","DOI":"10.1097\/DAD.0000000000001067","volume":"40","author":"Wiedemeyer","year":"2018","journal-title":"Am J Dermatopathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1260","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1016\/j.ad.2013.02.017","article-title":"Microsatellite and genetic instability in patients with Muir-Torre syndrome","volume":"104","author":"Lorente-Lavirgen","year":"2013","journal-title":"Actas Dermosifiliogr."},{"key":"10.1016\/j.ad.2019.02.012_bib1265","doi-asserted-by":"crossref","first-page":"90","DOI":"10.1016\/0190-9622(95)90017-9","article-title":"The Muir-Torre syndrome: A 25-year retrospect","volume":"33","author":"Schwartz","year":"1995","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1270","first-page":"5248","article-title":"A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer","volume":"58","author":"Boland","year":"1998","journal-title":"Cancer Res."},{"key":"10.1016\/j.ad.2019.02.012_bib1275","doi-asserted-by":"crossref","first-page":"567","DOI":"10.1136\/jmg.2003.012997","article-title":"A genotype-phenotype correlation in HNPCC: Strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome","volume":"41","author":"Mangold","year":"2004","journal-title":"J Med Genet."},{"key":"10.1016\/j.ad.2019.02.012_bib1280","doi-asserted-by":"crossref","first-page":"393","DOI":"10.1007\/s10897-012-9552-4","article-title":"Screening for Muir-Torre syndrome using mismatch repair protein immunohistochemistry of sebaceous neoplasms","volume":"22","author":"Roberts","year":"2013","journal-title":"J Genet Couns."},{"key":"10.1016\/j.ad.2019.02.012_bib1285","doi-asserted-by":"crossref","first-page":"381","DOI":"10.1016\/j.jdcr.2015.08.011","article-title":"Glioblastoma multiforme as initial internal malignancy in Muir-Torre syndrome (MTS)","volume":"1","author":"Lehrer","year":"2015","journal-title":"JAAD Case Rep."},{"key":"10.1016\/j.ad.2019.02.012_bib1290","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1097\/DSS.0000000000000376","article-title":"Muir-Torre syndrome and central nervous system malignancy: Highlighting an uncommon association","volume":"41","author":"Kurtzman","year":"2015","journal-title":"Dermatol Surg."},{"key":"10.1016\/j.ad.2019.02.012_bib1295","doi-asserted-by":"crossref","DOI":"10.5070\/D32311037239","article-title":"Lynch syndrome and Muir-Torre syndrome: An update and review on the genetics, epidemiology, and management of two related disorders","volume":"23","author":"Le","year":"2017","journal-title":"Dermatol Online J."},{"key":"10.1016\/j.ad.2019.02.012_bib1300","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1093\/jnci\/djk077","article-title":"Toward a consensus in molecular diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome)","volume":"99","author":"Lynch","year":"2007","journal-title":"J Natl Cancer Inst."},{"key":"10.1016\/j.ad.2019.02.012_bib1305","doi-asserted-by":"crossref","first-page":"1213","DOI":"10.1016\/j.humpath.2014.02.001","article-title":"BRAF\/KRAS gene sequencing of sebaceous neoplasms after mismatch repair protein analysis","volume":"45","author":"Cornejo","year":"2014","journal-title":"Hum Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1310","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1136\/jmedgenet-2011-100714","article-title":"Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: A literature review assessing utility of tumour features for MMR variant classification","volume":"49","author":"Parsons","year":"2012","journal-title":"J Med Genet."},{"key":"10.1016\/j.ad.2019.02.012_bib1315","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1111\/j.1749-6632.1999.tb09414.x","article-title":"BAP1, a candidate tumor suppressor protein that interacts with BRCA1","volume":"886","author":"Jensen","year":"1999","journal-title":"Ann N Y Acad Sci."},{"key":"10.1016\/j.ad.2019.02.012_bib1320","doi-asserted-by":"crossref","first-page":"1018","DOI":"10.1038\/ng.910","article-title":"Germline mutations in BAP1 predispose to melanocytic tumors","volume":"43","author":"Wiesner","year":"2011","journal-title":"Nat Genet."},{"key":"10.1016\/j.ad.2019.02.012_bib1325","doi-asserted-by":"crossref","first-page":"549","DOI":"10.1016\/j.jaad.2013.10.032","article-title":"Histopathologic clues for the diagnosis of Wiesner nevus","volume":"70","author":"Llamas-Velasco","year":"2014","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1330","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1001\/jamadermatol.2013.1529","article-title":"Multiple epithelioid Spitz nevi or tumors with loss of BAP1 expression: A clue to a hereditary tumor syndrome","volume":"149","author":"Busam","year":"2013","journal-title":"JAMA Dermatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1335","doi-asserted-by":"crossref","first-page":"564","DOI":"10.1111\/cup.12519","article-title":"BAP1-deficient and VE1-negative atypical Spitz tumor","volume":"42","author":"Requena","year":"2015","journal-title":"J Cutan Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1340","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1038\/nrgastro.2012.187","article-title":"Diagnosis of hepatitis E","volume":"10","author":"Aggarwal","year":"2013","journal-title":"Nat Rev Gastroenterol Hepatol."},{"key":"10.1016\/j.ad.2019.02.012_bib1345","doi-asserted-by":"crossref","first-page":"818","DOI":"10.1097\/PAS.0b013e3182498be5","article-title":"A distinct subset of atypical Spitz tumors is characterized by BRAF mutation and loss of BAP1 expression","volume":"36","author":"Wiesner","year":"2012","journal-title":"Am J Surg Pathol."},{"key":"10.1016\/j.ad.2019.02.012_bib1350","article-title":"Clinical and dermoscopic features of cutaneous BAP1 inactivated melanocytic tumors: Results of a multicenter case-control study by the International Dermoscopy Society (IDS)","author":"Y\u00e9lamos","year":"2018","journal-title":"J Am Acad Dermatol."}],"container-title":["Actas Dermo-Sifiliogr\u00e1ficas"],"original-title":[],"language":"es","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0001731019301772?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0001731019301772?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,11]],"date-time":"2025-09-11T01:09:41Z","timestamp":1757552981000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0001731019301772"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,11]]},"references-count":132,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2019,11]]}},"alternative-id":["S0001731019301772"],"URL":"https:\/\/doi.org\/10.1016\/j.ad.2019.02.012","relation":{},"ISSN":["0001-7310"],"issn-type":[{"value":"0001-7310","type":"print"}],"subject":[],"published":{"date-parts":[[2019,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"La biopsia cut\u00e1nea en el contexto de la enfermedad sist\u00e9mica","name":"articletitle","label":"Article Title"},{"value":"Actas Dermo-Sifiliogr\u00e1ficas","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ad.2019.02.012","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 AEDV. Published by Elsevier Espa\u00f1a, S.L.U. All rights reserved.","name":"copyright","label":"Copyright"}]}}