Kridin K, Sagi S, Bergman R. Mortality and cause of death in Israeli patients with pemphigus. Acta Derm. Venereol. [Internet]. 2017 [cited 2017 Mar 9];0. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28093595
Hsu DY, Brieva J, Sinha AA, Langan SM, Silverberg JI. Comorbidities and inpatient mortality for pemphigus in the USA. Br J Dermatol. 2016;174:1290–8.
CAS
Article
PubMed
Google Scholar
Tsunoda K, Ota T, Saito M, Hata T, Shimizu A, Ishiko A, et al. Pathogenic relevance of IgG and IgM antibodies against desmoglein 3 in blister formation in pemphigus vulgaris. Am. J. Pathol. [Internet]. 2011 [cited 2016 Feb 17];179:795–806. Available from: http://www.sciencedirect.com/science/article/pii/S0002944011004196
Pan M, Liu X, Zheng J. The pathogenic role of autoantibodies in pemphigus vulgaris. Clin. Exp. Dermatol. 2011. p. 703–7.
Joly P, Litrowski N. Pemphigus group (vulgaris, vegetans, foliaceus, herpetiformis, brasiliensis). Clin Dermatol. 2011;29:432–6.
Article
PubMed
Google Scholar
Amber KT, Staropoli P, Shiman MI, Elgart GW, Hertl M. Autoreactive T cells in the immune pathogenesis of pemphigus vulgaris. Exp Dermatol. 2013;22:699–704.
CAS
Article
PubMed
Google Scholar
Bystryn JC, Rudolph JL. Pemphigus. Lancet. 2005. p. 61–73.
Hammers CM, Stanley JR. Mechanisms of disease: pemphigus and bullous pemphigoid. Annu Rev Pathol Mech Dis [Internet]. 2016;11:175–97. Available from:. https://doi.org/10.1146/annurev-pathol-012615-044313.
CAS
Article
Google Scholar
Amagai M, Hashimoto T, Shimizu N, Nishikawa T. Absorption of pathogenic autoantibodies by the extracellular domain of pemphigus vulgaris antigen (Dsg3) produced by baculovirus. J Clin Invest. 1994;94:59–67.
CAS
Article
PubMed
PubMed Central
Google Scholar
Ahmed AR, Blose DA. Pemphigus vegetans: Neumann type and Hallopeau type. Int J Dermatol. 1984;23:135–41.
CAS
Article
PubMed
Google Scholar
Becker BA, Gaspari AA. Pemphigus vulgaris and vegetans. Dermatol Clin. 1993;11:429–52.
CAS
PubMed
Google Scholar
Hietanen J, Salo OP. Pemphigus: an epidemiological study of patients treated in Finnish hospitals between 1969 and 1978. Acta Derm Venereol. 1982;62:491–6.
CAS
PubMed
Google Scholar
Pisanti S, Sharav Y, Kaufman E, Posner LN. Pemphigus vulgaris: incidence in Jews of different ethnic groups, according to age, sex, and initial lesion. Oral Surg Oral Med Oral Pathol. 1974;38:382–7.
CAS
Article
PubMed
Google Scholar
Simon DG, Krutchkoff D, Kaslow RA, Zarbo R. Pemphigus in Hartford County, Connecticut, from 1972 to 1977. Arch Dermatol. 1980;116:1035–7.
CAS
Article
PubMed
Google Scholar
Adam BA. Bullous diseases in Malaysia: epidemiology and natural history. Int. J. Dermatol. [Internet]. 1992 [cited 2017 Dec 6];31:42–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1737688
Bastuji-Garin S, Souissi R, Blum L, Turki H, Nouira R, Jomaa B, et al. Comparative epidemiology of pemphigus in Tunisia and France: unusual incidence of pemphigus foliaceus in young Tunisian women. J Invest Dermatol [Internet]. 1995 [cited 2016 Feb 17];104:302–5. Available from: http://www.sciencedirect.com/science/article/pii/S0022202X15420500
Mahé A. Pemphigus in Mali: a study of 30 cases. Br J Dermatol. 1996;134:114–9.
Article
PubMed
Google Scholar
Micali G, Musumeci ML, Nasca MR. Epidemiologic analysis and clinical course of 84 consecutive cases of pemphigus in eastern Sicily. Int J Dermatol. 1998;37:197–200.
CAS
Article
PubMed
Google Scholar
Tsankov N, Vassileva S, Kamarashev J, Kazandjieva J, Kuzeva V. Epidemiology of pemphigus in Sofia, Bulgaria. A 16-year retrospective study (1980–1995). Int J Dermatol. 2000;39:104–8.
CAS
Article
PubMed
Google Scholar
Tallab T, Joharji H, Bahamdan K, Karkashan E, Mourad M, Ibrahim K. The incidence of pemphigus in the southern region of Saudi Arabia. Int J Dermatol. 2001;40:570–2.
CAS
Article
PubMed
Google Scholar
Hahn-Ristic K, Rzany B, Amagai M, Bröcker EB, Zillikens D. Increased incidence of pemphigus vulgaris in southern Europeans living in Germany compared with native Germans. J Eur Acad Dermatol Venereol. 2002;16:68–71.
CAS
Article
PubMed
Google Scholar
Nanda A, Dvorak R, Al-Saeed K, Al-Sabah H, Alsaleh QA. Spectrum of autoimmune bullous diseases in Kuwait. Int J Dermatol. 2004;43:876–81.
Article
PubMed
Google Scholar
Chams-Davatchi C, Valikhani M, Daneshpazhooh M, Esmaili N, Balighi K, Hallaji Z, et al. Pemphigus: analysis of 1209 cases. Int J Dermatol. 2005;44:470–6.
Article
PubMed
Google Scholar
Golušin Z, Poljački M, Jovanović M, Duran V, Stojanović S, Rajić N. Some epidemiological features of pemphigus chronicus in South Vojvodina: a 12-year retrospective study [2]. Int. J. Dermatol. 2005. p. 792–3.
Uzun S, Durdu M, Akman A, Gunasti S, Uslular C, Memisoglu HR, et al. Pemphigus in the Mediterranean region of Turkey: a study of 148 cases. Int. J. Dermatol. [Internet]. 2006 [cited 2016 Feb 17];45:523–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16700784
Salmanpour R, Shahkar H, Namazi MR, Rahman-Shenas MR. Epidemiology of pemphigus in south-western Iran: a 10-year retrospective study (1991-2000). Int. J. Dermatol. [Internet]. 2006 [cited 2017 Dec 2];45:103–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16445496
Michailidou EZ, Belazi MA, Markopoulos AK, Tsatsos MI, Mourellou ON, Antoniades DZ. Epidemiologic survey of pemphigus vulgaris with oral manifestations in northern Greece: retrospective study of 129 patients. Int J Dermatol. 2007;46:356–61.
Article
PubMed
Google Scholar
V’lckova-Laskoska MT, Laskoski DS, Kamberova S, Caca-Biljanovska N, Volckova N. Epidemiology of pemphigus in Macedonia: a 15-year retrospective study (1990–2004). Int J Dermatol. 2007;46:253–8.
Article
PubMed
Google Scholar
Langan SM, Smeeth L, Hubbard R, Fleming KM, Smith CJP, West J. Bullous pemphigoid and pemphigus vulgaris—incidence and mortality in the UK: population based cohort study. BMJ [Internet]. 2008;337:160–3. Available from: http://www.embase.com/search/results?subaction=viewrecord&from=export&id=L352039867
Google Scholar
Kumar KA. Incidence of pemphigus in Thrissur district, south India. Indian J Dermatol Venereol Leprol. 2008;74:349–51.
Article
PubMed
Google Scholar
Bertram F, Bröcker E-B, Zillikens D, Schmidt E. Prospective analysis of the incidence of autoimmune bullous disorders in Lower Franconia, Germany. J Dtsch Dermatol Ges [Internet]. 2009;7:434–40. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19170813
Google Scholar
Marazza G, Pham HC, Schärer L, Pedrazzetti PP, Hunziker T, Trüeb RM, et al. Incidence of bullous pemphigoid and pemphigus in Switzerland: A 2-year prospective study. Br. J Dermatol. 2009;161:861–8.
CAS
Article
PubMed
Google Scholar
Baican A, Baican C, Chiriac G, Chiriac MT, Macovei V, Zillikens D, et al. Pemphigus vulgaris is the most common autoimmune bullous disease in northwestern Romania. Int J Dermatol. 2010;49:768–74.
Article
PubMed
Google Scholar
Zaraa I, Kerkeni N, Ishak F, Zribi H, El Euch D, Mokni M, et al. Spectrum of autoimmune blistering dermatoses in Tunisia: an 11-year study and a review of the literature. Int. J. Dermatol. [Internet]. 2011 [cited 2016 Feb 17];50:939–44. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21781064
Marinovic B, Lipozencic J, Jukic IL. Autoimmune blistering diseases: incidence and treatment in Croatia. Dermatol. Clin. 2011. p. 677–9.
Huang Y-H, Kuo C-F, Chen Y-H, Yang Y-W. Incidence, mortality, and causes of death of patients with pemphigus in Taiwan: a nationwide population-based study. J Invest Dermatol. [Internet]. 2012;132:92–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21850023
CAS
Article
Google Scholar
Bozdag K, Bilgin İ. Epidemiology of pemphigus in the western region of Turkey: retrospective analysis of 87 patients. Cutan Ocul Toxicol [Internet]. 2012;31:280–5. Available from:. https://doi.org/10.3109/15569527.2011.653598.
CAS
Article
Google Scholar
Kridin K, Zelber-Sagi S, Khamaisi M, Cohen AD, Bergman R. Remarkable differences in the epidemiology of pemphigus among two ethnic populations in the same geographic region. J. Am. Acad. Dermatol. [Internet]. 2016 [cited 2016 Oct 14]; Available from: http://www.ncbi.nlm.nih.gov/pubmed/27614531
Milinković M V., Janković S, Medenica L, Nikolić M, Reljić V, Popadić S, et al. Incidence of autoimmune bullous diseases in Serbia: a 20-year retrospective study. JDDG J. der Dtsch. Dermatologischen Gesellschaft [Internet]. 2016 [cited 2017 Sep 3];14:995–1005. Available from: http://www.ncbi.nlm.nih.gov/pubmed/27767273
Kridin K, Zelber-Sagi S, Bergman R. Pemphigus vulgaris and pemphigus foliaceus: differences in epidemiology and mortality. Acta Derm. Venereol. [Internet]. 2017;0. Available from: https://doi.org/10.2340/00015555-2706
Ahmed AR, Wagner R, Khatri K, Notani G, Awdeh Z, Alper CA, et al. Major histocompatibility complex haplotypes and class II genes in non-Jewish patients with pemphigus vulgaris. Proc. Natl. Acad. Sci. U. S. A. [Internet]. 1991;88:5056–60. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=51806&tool=pmcentrez&rendertype=abstract
CAS
Article
Google Scholar
Ahmed AR, Yunis EJ, Khatri K, Wagner R, Notani G, Awdeh Z, et al. Major histocompatibility complex haplotype studies in Ashkenazi Jewish patients with pemphigus vulgaris. Proc Natl Acad Sci U S A. 1990;87:7658–62.
CAS
Article
PubMed
PubMed Central
Google Scholar
Krain LS. Increased frequency of HL-A10 in pemphigus vulgaris. Arch. Dermatol. [Internet]. American Medical Association; 1973 [cited 2016 Feb 17];108:803. Available from: http://archderm.jamanetwork.com/article.aspx?articleid=533634
Mobini N, Yunis EJ, Alper CA, Yunis JJ, Delgado JC, Yunis DE, et al. Identical MHC markers in non-Jewish Iranian and Ashkenazi Jewish patients with pernphigus vulgaris: possible common central Asian ancestral origin. Hum Immunol. 1997;57:62–7.
CAS
Article
PubMed
Google Scholar
Sarig O, Bercovici S, Zoller L, Goldberg I, Indelman M, Nahum S, et al. Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. J Invest Dermatol. [Internet]. 2012;132:1798–805. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22437316
CAS
Article
Google Scholar
Bystryn JC, Steinman NM. The adjuvant therapy of pemphigus. An update. Arch Dermatol. [Internet]. 1996;132:203–12. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8629830
CAS
Article
Google Scholar
Risser J, Lewis K, Weinstock MA. Mortality of bullous skin disorders from 1979 through 2002 in the United States. Arch Dermatol. 2009;145:1005–8.
Article
PubMed
Google Scholar
Ahmed AR, Moy R. Death in pemphigus. J Am Acad Dermatol. 1982;7:221–8.
CAS
Article
PubMed
Google Scholar
Anhalt GJ. Making sense of antigens and antibodies in pemphigus. J Am Acad Dermatol. 1999;40:763–6.
CAS
Article
PubMed
Google Scholar
Mahoney MG, Wang Z, Rothenberger K, Koch PJ, Amagai M, Stanley JR. Explanations for the clinical and microscopic localization of lesions in pemphigus foliaceus and vulgaris. J Clin Invest. 1999;103:461–8.
CAS
Article
PubMed
PubMed Central
Google Scholar
Scott JE, Ahmed AR. The blistering diseases. Med Clin North Am. 1998. p. 1239–83.
Khachemoune A, Guldbakke KK, Ehrsam E. Pemphigus foliaceus: a case report and short review. Cutis [Internet]. 2006 [cited 2017 Nov 24];78:105–10. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16983898
Amerian ML, Ahmed AR. Pemphigus erythematosus: Senear-Usher syndrome. Int. J. Dermatol. 1985. p. 16–25.
Diaz LA, Sampaio SAP, Rivitti EA, Martins CR, Cunha PR, Lombardi C, et al. Endemic pemphigus foliaceus (fogo selvagem): II. Current and historic epidemiologic studies. J Invest Dermatol [Internet]. 1989;92:4–12. Available from: http://linkinghub.elsevier.com/retrieve/pii/S0022202X89906829
CAS
Article
Google Scholar
Korman NJ. New immunomodulating drugs in autoimmune blistering diseases. Dermatol Clin. 2001. p. 637–48.
Amagai M. Pemphigus. In: Bolognia JL, Jorizzo JL, Schaffer J V, editors. Dermatology. Third. Elsevier; 2012. p. 461–73.
Abreau-Velez AM, Hashimoto T, Bollag WB, Arroyave ST, Abreau-Velez CE, Londoeo ML, et al. A unique form of endemic pemphigus in northern Colombia. J Am Acad Dermatol. 2003;49:599–608.
Article
Google Scholar
Stanley J. Pemphigus. In: Wolff K, Goldsmith LA, Katz SI, et al., editors. Fitzpatrick’s dermatology in general medicine. New York, McGraw-Hill; 2008. p. 459–68.
Del Mar Sáez-de-Ocariz M, Vega-Memije ME, Zúñiga J, Salgado N, Ruíz J, Balbuena A, et al. HLA-DRB1*0101 is associated with foliaceous pemphigus in Mexicans. Int. J. Dermatol. 2005. p. 350.
De Sena Nogueira Maehara L, De-Souza-Santana FC, Porro AM, Marcos EVC, Ura S, Nolte IM, et al. HLA class II alleles of susceptibility and protection in Brazilian and Dutch pemphigus foliaceus. Br. J. Dermatol. [Internet]. 2017 [cited 2017 Nov 25]; Available from: https://doi.org/10.1111/bjd.16022
Lombardi ML, Mercuro O, Ruocco V, Lo Schiavo A, Lombari V, Guerrera V, et al. Common human leukocyte antigen alleles in pemphigus vulgaris and pemphigus foliaceus Italian patients. J Invest Dermatol [Internet]. 1999;113:107–10. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10417627
CAS
Article
Google Scholar
Loiseau P, Lecleach L, Prost C, Lepage V, Busson M, Bastuji-Garin S, et al. HLA class II polymorphism contributes to specify desmoglein derived peptides in pemphigus vulgaris and pemphigus foliaceus. J Autoimmun. 2000;15:67–73.
CAS
Article
PubMed
Google Scholar
Diaz LA, Sampaio SA, Rivitti EA, Martins CR, Cunha PR, Lombardi C, et al. Endemic pemphigus foliaceus (fogo selvagem). I. Clinical features and immunopathology. J Am Acad Dermatol. 1989;20:657–69.
CAS
Article
PubMed
Google Scholar
Empinotti JC, Aoki V, Filgueira A, Sampaio SAP, Rivitti EA, Sanches JA, et al. Clinical and serological follow-up studies of endemic pemphigus foliaceus (fogo selvagem) in western Parana, Brazil (2001–2002). Br J Dermatol. 2006;155:446–50.
CAS
Article
PubMed
Google Scholar
Culton DA, Qian Y, Li N, Rubenstein D, Aoki V, Filhio GH, et al. Advances in pemphigus and its endemic pemphigus foliaceus (fogo selvagem) phenotype: a paradigm of human autoimmunity. J Autoimmun. 2008;31:311–24.
CAS
Article
PubMed
PubMed Central
Google Scholar
Diaz LA, Arteaga LA, Hilario-Vargas J, Valenzuela JG, Li N, Warren S, et al. Anti-desmoglein-1 antibodies in onchocerciasis, leishmaniasis and chagas disease suggest a possible etiological link to fogo selvagem. J Invest Dermatol. 2004;123:1045–51.
CAS
Article
PubMed
Google Scholar
Qian Y, Clarke SH, Aoki V, Hans-Filhio G, Rivitti EA, Diaz LA. Antigen selection of anti-DSG1 autoantibodies during and before the onset of endemic pemphigus foliaceus. J Invest Dermatol. 2009;129:2823–34.
CAS
Article
PubMed
PubMed Central
Google Scholar
Aoki V, Rivitti EA, Diaz LA, Cooperative Group on Fogo Selvagem Research. Update on fogo selvagem, an endemic form of pemphigus foliaceus. J. Dermatol. [Internet]. 2015 [cited 2017 Nov 27];42:18–26. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25558948
Robledo MA, Prada S, Jaramillo D, Leon W. South American pemphigus foliaceus: study of an epidemic in El Bagre and Nechi, Colombia 1982 to 1986. Br. J Dermatol. 1988;118:737–44.
CAS
Article
PubMed
Google Scholar
Abida O, Zitouni M, Kallel-Sellami M, Mahfoudh N, Kammoun A, Ben Ayed M, et al. Tunisian endemic pemphigus foliaceus is associated with the HLA-DR3 gene: anti-desmoglein 1 antibody-positive healthy subjects bear protective alleles. Br J Dermatol. 2009;161:522–7.
CAS
Article
PubMed
Google Scholar
Abida O, Masmoudi A, Rebaï A, Ben Ayed M, Mahfoudh N, Kallel-Sellami M, et al. The familial feature of Tunisian endemic pemphigus foliaceus. Br. J. Dermatol. 2009. p. 951–3.
Joly P, Mokhtar I, Gilbert D, Thomine E, Fazza B, Bardi R, et al. Immunoblot and immunoelectronmicroscopic analysis of endemic Tunisian pemphigus. Br J Dermatol. 1999;140:44–9.
CAS
Article
PubMed
Google Scholar
Kallel Sellami M, Ben Ayed M, Mouquet H, Drouot L, Zitouni M, Mokni M, et al. Anti-desmoglein 1 antibodies in Tunisian healthy subjects: arguments for the role of environmental factors in the occurrence of Tunisian pemphigus foliaceus. Clin Exp Immunol. 2004;137:195–200.
CAS
Article
PubMed
PubMed Central
Google Scholar
Leshem YA, Katzenelson V, Yosipovitch G, David M, Mimouni D. Autoimmune diseases in patients with pemphigus and their first-degree relatives. Int J Dermatol. 2011;50:827–31.
Article
PubMed
Google Scholar
Parameswaran A, Attwood K, Sato R, Seiffert-Sinha K, Sinha AA. Identification of a new disease cluster of pemphigus vulgaris with autoimmune thyroid disease, rheumatoid arthritis and type I diabetes. Br J Dermatol. 2015;172:729–38.
CAS
Article
PubMed
Google Scholar
Chiu Y-W, Chen Y-D, Hua T-C, Wu C-H, Liu H-N, Chang Y-T Comorbid autoimmune diseases in patients with pemphigus: a nationwide case-control study in Taiwan. Eur. J. Dermatol. [Internet]. 2017 [cited 2017 Dec 2];27:375–81. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28747284
Kridin K, Zelber-Sagi S, Comaneshter D, Cohen AD. Ulcerative colitis associated with pemphigus: a population-based large-scale study. Scand J Gastroenterol. 2017;52:1360–4.
Article
PubMed
Google Scholar
Firooz A, Mazhar A, Ahmed AR. Prevalence of autoimmune diseases in the family members of patients with pemphigus vulgaris. J Am Acad Dermatol. 1994;3:434–7.
Article
Google Scholar
Kridin K, Zelber-Sagi S, Comaneshter D, Cohen AD. Association between pemphigus and psoriasis: a population-based large-scale study. J. Am. Acad. Dermatol. [Internet]. 2017 [cited 2017 Dec 2];77:1174–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/29132851
Lee CW, Ro YS, Kim JH. Concurrent development of pemphigus foliaceus and psoriasis. Int. J. Dermatol. [Internet]. 1985 [cited 2017 Feb 12];24:316–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/4018981
Aghassi D, Dover JS. Pemphigus foliaceus induced by psoralen-UV-A. Arch. Dermatol. [Internet]. 1998 [cited 2017 Feb 12];134:1300–1. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9801700
Lee CW, Ro YS. Pemphigus developed on preexisting dermatoses. J. Dermatol. [Internet]. 1994 [cited 2017 Feb 12];21:213–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8014278
Tomasini D, Cerri A, Cozzani E, Berti E. Development of pemphigus foliaceus in a patient with psoriasis: a simple coincidence? Eur. J. Dermatol. [Internet]. [cited 2017 Feb 12];8:56–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9649683
Yokoo M, Oka D, Ueki H. Coexistence of psoriasis vulgaris and pemphigus foliaceus. Dermatologica [Internet]. 1989 [cited 2017 Feb 12];179:222–3. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2620759
Perez GL, Agger WA, Abellera RM, Dahlberg P. Pemphigus foliaceus coexisting with IgA nephropathy in a patient with psoriasis vulgaris. Int. J. Dermatol. [Internet]. 1995 [cited 2017 Feb 12];34:794–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8543414
Giomi B, Cardinali C, Pestelli E, Caproni M, Fabbri P. Pemphigus foliaceus developing on pre-existing psoriasis: a supposed pathogenetic linkage. Acta Derm. Venereol. [Internet]. 2004 [cited 2017 Feb 12];84:82–3. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15040491
Kurtzman DJB, Christopher M, Lian F, Sligh JE. A blistering response: concurrent psoriasis and pemphigus foliaceus. Am. J. Med. [Internet]. 2015 [cited 2017 Feb 12];128:24–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25239159
Kwon HH, Kwon IH, Chung JH, Youn, J Il. Pemphigus foliaceus associated with psoriasis during the course of narrow-band UVB therapy: a simple coincidence? Ann. Dermatol. [Internet]. 2011 [cited 2017 Feb 12];23:S281–4. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3276776&tool=pmcentrez&rendertype=abstract
Panzarella K, Camisa C. Coexistence of superficial pemphigus and psoriasis. Cutis [Internet]. 1996 [cited 2017 Feb 12];57:414–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8804843
Caldarola G, Carbone A, De Simone C, Pellicano R. Development of pemphigus vulgaris in a patient with psoriasis treated with cyclosporine. J. Am. Acad. Dermatol. [Internet]. 2010 [cited 2017 Feb 13];63:356–7. Available from: http://linkinghub.elsevier.com/retrieve/pii/S0190962209006689
Fye KH, Tanenbaum L Penicillamine-induced pemphigus vulgaris in psoriatic arthritis. J. Rheumatol. [Internet]. [cited 2017 Feb 12];9:331–2. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7097698
Fryer EJ, Lebwohl M Pemphigus vulgaris after initiation of psoralen and UVA therapy for psoriasis. J. Am. Acad. Dermatol. [Internet]. 1994 [cited 2017 Feb 12];30:651–3. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8157795
Reis VM, Toledo RP, Lopez A, Diaz LA, Martins JE. UVB-induced acantholysis in endemic pemphigus foliaceus (Fogo selvagem) and Pemphigus vulgaris. J. Am. Acad. Dermatol. [Internet]. 2000 [cited 2017 Feb 12];42:571–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10727300
Grunwald MH, David M, Feuerman EJ. Coexistence of psoriasis vulgaris and bullous diseases. J. Am. Acad. Dermatol. [Internet]. 1985 [cited 2017 Feb 13];13:224–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/3900156
Ogawa H, Sakuma M, Morioka S, Kitamura K, Sasai Y, Imamura S, et al. The incidence of internal malignancies in pemphigus and bullous pemphigoid in Japan. J Dermatol Sci. 1995;9:136–41.
CAS
Article
PubMed
Google Scholar
Schulze F, Neumann K, Recke A, Zillikens D, Linder R, Schmidt E. Malignancies in pemphigus and pemphigoid diseases. J. Invest. Dermatol. [Internet]. 2015 [cited 2017 Apr 14];135:1445–7. Available from: https://ssl.haifa.ac.il/S0022202X15372419/,DanaInfo=.aadBhpxEjlwJn0z+1-s2.0-S0022202X15372419-main.pdf?_tid=48c2b632-211b-11e7-ab18-00000aab0f26&acdnat=1492178852_19abf9717daebe91b688e3cbd8fcbc2e
Kridin K, Zelber-Sagi S, Comaneshter D, Batat E, Cohen AD. Pemphigus and hematologic malignancies: a population-based study of 11,859 patients. J. Am. Acad. Dermatol. [Internet]. Elsevier; 2017 [cited 2017 Dec 2];0. Available from: http://linkinghub.elsevier.com/retrieve/pii/S019096221732738X
Kridin K, Zelber-Sagi S, Comaneshter D, Cohen AD. Bipolar disorder associated with another autoimmune disease—pemphigus: a population-based study. Can. J. Psychiatry [Internet]. 2017 [cited 2017 Dec 2];70674371774034. Available from: http://www.ncbi.nlm.nih.gov/pubmed/29108425
Kridin K, Zelber-Sagi S, Comaneshter D, Cohen AD. Association between schizophrenia and an autoimmune bullous skin disease-pemphigus: a population-based large-scale study. Epidemiol. Psychiatr. Sci. [Internet]. 2017 [cited 2017 Dec 2];1–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28942756
Wohl Y, Mashiah J, Kutz A, Hadj-Rabia S, Cohen AD. Pemphigus and depression comorbidity: a case control study. Eur J Dermatology. 2015;25:602–5.
CAS
Google Scholar
Kumar V, Mattoo SK, Handa S. Psychiatric morbidity in pemphigus and psoriasis: a comparative study from India. Asian J Psychiatr. 2013;6:151–6.
Article
PubMed
Google Scholar
Arbabi M, Ghodsi Z, Mahdanian A, Noormohammadi N, Shalileh K, Darvish F, et al. Mental health in patients with pemphigus: an issue to worth consideration. Indian J. Dermatol. [Internet]. Medknow Publications; 2011 [cited 2017 Apr 30];56:541–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22121274
Tabolli S, Mozzetta A, Antinone V, Alfani S, Cianchini G, Abeni D. The health impact of pemphigus vulgaris and pemphigus foliaceus assessed using the medical outcomes study 36-item short form health survey questionnaire. Br. J. Dermatol. [Internet]. 2008;158:1029–34. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18294312
Tabolli S, Pagliarello C, Paradisi A, Cianchini G, Giannantoni P, Abeni D. Burden of disease during quiescent periods in patients with pemphigus. Br J Dermatol. 2014;170:1087–91.
CAS
Article
PubMed
Google Scholar
Kridin K, Zelber-Sagi S, Comaneshter D, Cohen AD. Association between pemphigus and neurologic diseases. JAMA Dermatol. 2018. https://doi.org/10.1001/jamadermatol.2017.5799
Ren Z, Hsu DY, Brieva J, Silverberg NB, Langan SM, Silverberg JI. Hospitalization, inpatient burden and comorbidities associated with bullous pemphigoid in the U.S.A. Br J Dermatol. 2017;176:87–99.
CAS
Article
PubMed
Google Scholar
Wohl Y, Dreiher J, Cohen AD. Pemphigus and osteoporosis: a case-control study. Arch Dermatol [Internet]. 2010;146:1126–31. Available from: file://o/Referenzmanager/Immunglobulin.PDFs/Wohl2010.pdf
Tee S-I. Prevention of glucocorticoid-induced osteoporosis in immunobullous diseases with alendronate. Arch. Dermatol. [Internet]. 2012;148:307. Available from: https://doi.org/10.1001/archdermatol.2011.354
Harman M, Uçmak F, Akpolat V, Uçmak D. The frequency of osteoporosis in patients with pemphigus vulgaris on treatment. Indian J. Dermatology, Venereol. Leprol. [Internet]. 2013 [cited 2017 Dec 10];79:211. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23442460
Anhalt GJ, Kim S, Stanley JR, Korman NJ, Jabs DA, Kory M, et al. Paraneoplastic pemphigus. N Engl J Med [Internet]. 1990;323:1729–35. Available from:. https://doi.org/10.1056/NEJM199012203232503.
CAS
Article
Google Scholar
Anhalt GJ. Paraneoplastic pemphigus. J. Investig. Dermatology Symp. Proc. 2004. p. 29–33.
Kim SC, Kwon Y, Do LIJ, Lee IJ, Chang SN, Lee TG. cDNA cloning of the 210-kDa paraneoplastic pemphigus antigen reveals that envoplakin is a component of the antigen complex. J Invest Dermatol. 1997;109:365–9.
CAS
Article
PubMed
Google Scholar
Mahoney MG, Aho S, Uitto J, Stanley JR. The members of the plakin family of proteins recognized by paraneoplastic pemphigus antibodies include periplakin. J Invest Dermatol. 1998;111:308–13.
CAS
Article
PubMed
Google Scholar
Schepens I, Jaunin F, Begre N, Läderach U, Marcus K, Hashimoto T, et al. The protease inhibitor alpha-2-macroglobuline-like-1 is the p170 antigen recognized by paraneoplastic pemphigus autoantibodies in human. PLoS One. 2010;5(8).
Zimmermann J, Bahmer F, Rose C, Zillikens D, Schmidt E. Clinical and immunopathological spectrum of paraneoplastic pemphigus. JDDG J der Dtsch Dermatologischen Gesellschaft [Internet]. 2010;8:598–605. Available from:. https://doi.org/10.1111/j.1610-0387.2010.07380.x.
Google Scholar
Wieczorek M, Czernik A. Paraneoplastic pemphigus: a short review. Clin Cosmet Investig Dermatol. 2016;9:291–5.
Article
PubMed
PubMed Central
Google Scholar
Mimouni D, Anhalt GJ, Lazarova Z, Aho S, Kazerounian S, Kouba DJ, et al. Paraneoplastic pemphigus in children and adolescents. Br. J. Dermatol. [Internet]. 2002 [cited 2017 Nov 21];147:725–32. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12366419
Leger S, Picard D, Ingen-Housz-Oro S, Arnault J-P, Aubin F, Carsuzaa F, et al. Prognostic factors of paraneoplastic pemphigus. Arch Dermatol [Internet]. 2012;148:1165. Available from:. https://doi.org/10.1001/archdermatol.2012.1830.
Article
Google Scholar
Ohzono A, Sogame R, Li X, Teye K, Tsuchisaka A, Numata S, et al. Clinical and immunological findings in 104 cases of paraneoplastic pemphigus. Br J Dermatol. 2015;173:1447–52.
CAS
Article
PubMed
Google Scholar
Martel P, Loiseau P, Joly P, Busson M, Lepage V, Mouquet H, et al. Paraneoplastic pemphigus is associated with the DRB1*03 allele. J. Autoimmun. [Internet]. 2003 [cited 2017 Nov 21];20:91–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12604316
Liu Q, Bu DF, Li D, Zhu XJ. Genotyping of HLA-I and HLA-II alleles in Chinese patients with paraneoplastic pemphigus. Br J Dermatol. 2008;158:587–91.
CAS
Article
PubMed
Google Scholar
Kaplan I, Hodak E, Ackerman L, Mimouni D, Anhalt GJ, Calderon S. Neoplasms associated with paraneoplastic pemphigus: a review with emphasis on non-hematologic malignancy and oral mucosal manifestations. Oral Oncol. 2004. p. 553–62.
Joly P, Richard C, Gilbert D, Courville P, Chosidow O, Roujeau JC, et al. Sensitivity and specificity of clinical, histologic, and immunologic features in the diagnosis of paraneoplastic pemphigus. J Am Acad Dermatol. 2000;43:619–26.
CAS
Article
PubMed
Google Scholar
Anhalt GJ. Paraneoplastic pemphigus. J. Investig. Dermatology Symp. Proc. [Internet]. 2004 [cited 2017 Nov 22];9:29–33. Available from: http://www.ncbi.nlm.nih.gov/pubmed/14870982
Nguyen VT, Ndoye A, Bassler KD, Shultz LD, Shields MC, Ruben BS, et al. Classification, clinical manifestations, and immunopathological mechanisms of the epithelial variant of paraneoplastic autoimmune multiorgan syndrome: a reappraisal of paraneoplastic pemphigus. Arch Dermatol. 2001;137:193–206.
CAS
PubMed
Google Scholar
Czernik A, Camilleri M, Pittelkow MR, Grando SA. Paraneoplastic autoimmune multiorgan syndrome: 20 years after. Int. J. Dermatol. 2011. p. 905–14.
Fullerton SH, Woodley DT, Smoller BR, Anhalt GJ. Paraneoplastic pemphigus with autoantibody deposition in bronchial epithelium after autologous bone marrow transplantation. JAMA [Internet]. 1992;267:1500–2. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1538540
Maldonado F, Pittelkow MR, Ryu JH. Constrictive bronchiolitis associated with paraneoplastic autoimmune multi-organ syndrome. Respirology. 2009. p. 129–33.
Nikolskaia OV, Nousari CH, Anhalt GJ. Paraneoplastic pemphigus in association with Castleman’s disease. Br J Dermatol. 2003;149:1143–51.
CAS
Article
PubMed
Google Scholar
Tsuchisaka A, Numata S, Teye K, Natsuaki Y, Kawakami T, Takeda Y, et al. Epiplakin is a paraneoplastic pemphigus autoantigen and related to bronchiolitis obliterans in Japanese patients. J Invest Dermatol. 2016;136:399–408.
CAS
Article
PubMed
Google Scholar
Jablonska S, Chorzelski TP, Beutner EH, Chorzelska J. Herpetiform pemphigus, a variable pattern of pemphigus. Int J Dermatol. 1975;14:353–9.
CAS
Article
PubMed
Google Scholar
Kasperkiewicz M, Kowalewski C, Jabłońska S. Pemphigus herpetiformis: from first description until now. J Am Acad Dermatol. 2014;70:780–7.
Article
PubMed
Google Scholar
Porro AM, Caetano de LVN, Maehara de LSN, dos Enokihara MMS. Non-classical forms of pemphigus: pemphigus herpetiformis, IgA pemphigus, paraneoplastic pemphigus and IgG/IgA pemphigus. An. Bras. Dermatol. 2014. p. 96–106.
Robinson ND, Hashimoto T, Amagai M, Chan LS. The new pemphigus variants. J. Am. Acad. Dermatol. 1999. p. 649–71.
Hocar O, Ait Sab I, Akhdari N, Hakkou M, Amal S. A case of pemphigus herpetiformis in a 12-year-old male. Int Sch Res Netw Pediatr. 2011;2011:1–4.
Google Scholar
Leithauser LA, Mutasim DF. A case of pemphigus herpetiformis occurring in a 9-year-old boy. Pediatr Dermatol. 2013;30:760–2.
Article
PubMed
Google Scholar
Moutran R, Maatouk I, Stephan F, Halaby E, Abadjian G, Tomb R. Letter: Pemphigus herpetiformis of age of onset at 6 years. Dermatol Online J. 2011;17
Maciejowska E, Jablonska S, Chorzelski T. Is pemphigus herpetiformis an entity? Int J Dermatol. 1987;26:571–7.
CAS
Article
PubMed
Google Scholar
Santi CG, Maruta CW, Aoki V, Sotto MN, Rivitti EA, Diaz LA. Pemphigus herpetiformis is a rare clinical expression of nonendemic pemphigus foliaceus, fogo selvagem, and pemphigus vulgaris. J Am Acad Dermatol. 1996;34:40–6.
CAS
Article
PubMed
Google Scholar
Morini JP, Jomaa B, Gorgi Y, Saguem MH, Nouira R, Roujeau JC, et al. Pemphigus foliaceus in young women. An endemic focus in the Sousse area of Tunisia. Arch Dermatol [Internet]. 1993;129:69–73. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8420494
CAS
Article
Google Scholar
Laws PM, Heelan K, Al-Mohammedi F, Walsh S, Shear NH. Pemphigus herpetiformis: a case series and review of the literature. Int J Dermatol. 2015;54:1014–22.
CAS
Article
PubMed
Google Scholar
Muramatsu T, Iida T, Honoki K, Nakatani C, Hatoko M, Shirai T, et al. Pemphigus vulgaris preceded by herpetiform-like skin lesions with negative immunofluorescence findings. J Dermatol [Internet]. 1999;26:154–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10209921
CAS
Article
Google Scholar
Lebeau S, Müller R, Masouyé I, Hertl M, Borradori L. Pemphigus herpetiformis: analysis of the autoantibody profile during the disease course with changes in the clinical phenotype. Clin Exp Dermatol. 2010;35:366–72.
CAS
Article
PubMed
Google Scholar
Palleschi GM, Giomi B. Herpetiformis pemphigus and lung carcinoma: a case of paraneoplastic pemphigus. Acta Derm. Venereol. 2002. p. 304–5.
Prado R, Brice SL, Fukuda S, Hashimoto T, Fujita M. Paraneoplastic pemphigus herpetiformis with IgG antibodies to desmoglein 3 and without mucosal lesions. Arch Dermatol [Internet]. 2011;147:67. Available from:. https://doi.org/10.1001/archdermatol.2010.362.
Article
Google Scholar
Arranz D, Corral M, Prats I, López-Ayala E, Castillo C, Vidaurrázaga C, et al. Herpetiform pemphigus associated with esophageal carcinoma. Actas Dermosifiliogr. 2005. p. 119–21.
Marzano A V, Tourlaki A, Cozzani E, Gianotti R, Caputo R. Pemphigus herpetiformis associated with prostate cancer. J. Eur. Acad. Dermatol. Venereol. [Internet]. 2007 [cited 2017 Nov 20];21:696–8. Available from: https://doi.org/10.1111/j.1468-3083.2006.01992.x
Lu Y, Zhang M. Pemphigus herpetiformis in a patient with well-differentiated cutaneous angiosarcoma: case report and review of the published work. J. Dermatol. [Internet]. 2012 [cited 2017 Nov 20];39:89–91. Available from: https://doi.org/10.1111/j.1346-8138.2011.01287.x
Sanchez-Palacios C, Chan LS. Development of pemphigus herpetiformis in a patient with psoriasis receiving UV-light treatment. J Cutan Pathol. 2004;31:346–9.
Article
PubMed
Google Scholar
Morita E, Amagai M, Tanaka T, Horiuchi K, Mizuno H, Yamamoto S. A case of herpetiform pemphigus coexisting with psoriasis vulgaris [6]. Br. J. Dermatol. 1999. p. 754–5.
Marinović B, Basta-Juzbašić A, Bukvić-Mokos Z, Ľeović R, Lončrić D. Coexistence of pemphigus herpetiformis and systemic lupus erythematosus. J Eur Acad Dermatology Venereol. 2003;17:316–9.
Article
Google Scholar
Shimizu K, Hashimoto T, Wang N, Watanabe K, Ohata Y, Kikuchi A, et al. A case of herpetiform pemphigus associated with autoimmune hemolytic anemia: detection of autoantibodies against multiple epidermal antigens. Dermatology [Internet]. 1996 [cited 2017 Nov 20];192:179–82. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8829509
Bull RH, Fallowfield ME, Marsden RA. Autoimmune blistering diseases associated with HIV infection. Clin Exp Dermatol. 1994;19:47–50.
CAS
Article
PubMed
Google Scholar
Abe T, Kouno M, Yamamoto N, Mori O, Hashimoto T, Amagai M. A case of D-penicillamine induced herpetiform pemphigus. Nishinihon J Dermatol. 2003;65:126–9.
Article
Google Scholar
Weltfriend S, Ingber A, David M, Sandbank M. Pemphigus herpetiformis following D-penicillamine in a patient with HLA B8. Hautarzt. [Internet]. 1988 [cited 2017 Nov 20];39:587–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2972666
Verdier-Sevrain S, Joly P, Thomine E, Belanyi P, Gilbert D, Tron F, et al. Thiopronine-induced herpetiform pemphigus: report of a case studied by immunoelectron microscopy and immunoblot analysis. Br. J. Dermatol. [Internet]. 1994 [cited 2017 Nov 20];130:238–40. Available from: http://www.ncbi.nlm.nih.gov/pubmed/8123578
Tsuruta D, Ishii N, Hamada T, Ohyama B, Fukuda S, Koga H, et al. IgA pemphigus. Clin Dermatol. 2011;29:437–42.
Article
PubMed
Google Scholar
Geller S, Gat A, Zeeli T, Hafner A, Eming R, Hertl M, et al. The expanding spectrum of IgA pemphigus: a case report and review of the literature. Br. J. Dermatol. 2014. p. 650–6.
Hodak E, David M, Ingber A, Rotem A, Hazaz B, Shamai-lubovitz O, et al. The clinical and histopathological spectrum of IgA-pemphigus—report of two cases. Clin Exp Dermatol. 1990;15:433–7.
CAS
Article
PubMed
Google Scholar
Hashimoto T, Kiyokawa C, Mori O, Miyasato M, Chidgey MAJ, Garrod DR, et al. Human desmocollin 1 (Dsc1) is an autoantigen for the subcorneal pustular dermatosis type of IgA pemphigus. J. Invest. Dermatol. 1997;109:127–31.
CAS
Article
PubMed
Google Scholar
Ishii N, Ishida-Yamamoto A, Hashimoto T. Immunolocalization of target autoantigens in IgA pemphigus. Clin Exp Dermatol. 2004;29:62–6.
CAS
Article
PubMed
Google Scholar
Tajima M, Mitsuhashi Y, Irisawa R, Amagai M, Hashimoto T, Tsuboi R. IgA pemphigus reacting exclusively to desmoglein 3. Eur. J. Dermatol. [Internet]. [cited 2017 Nov 23];20:626–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20605770
Ljubojevic S, Lipozenčić J. Autoimmune bullous diseases associations. Clin. Dermatol. [Internet]. 2012 [cited 2017 Sep 3];30:17–33. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22137223
Wallach D. Intraepidermal IgA pustulosis. J. Am. Acad. Dermatol. [Internet]. 1992 [cited 2017 Nov 23];27:993–1000. Available from: http://www.ncbi.nlm.nih.gov/pubmed/1479108
Kern J, Gehring W, Kreisel W, Hertl M, Technau-Hafsi K, Bruckner-Tuderman L, et al. Overlap of IgA pemphigus and linear IgA dermatosis in a patient with ulcerative colitis: a mere coincidence? Acta Derm. Venereol. [Internet]. 2014 [cited 2017 Jan 7];94:228–30. Available from: https://doi.org/10.2340/00015555-1658
Sotiriou MC, Foo CW, Scholes CT, Zone JJ. Immunobullous disease and ulcerative colitis: a case series of six patients. Br. J. Dermatol. [Internet]. 2015 [cited 2017 Dec 2];173:792–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25913891
Papakonstantinou E, Kapp A, Jonkman MF, Raap U. Intraepidermal neutrophilic dermatosis type of IgA pemphigus with circulating linear IgA disease antibodies associated with ulcerative colitis. J. Eur. Acad. Dermatology Venereol. [Internet]. 2017 [cited 2017 Dec 2]; Available from: http://www.ncbi.nlm.nih.gov/pubmed/28653439
Cetkovská P, Komorousová M, Lomicová I. Management of a pemphigus with IgA and IgG antibodies and coexistent lung cancer. Dermatol. Ther. [Internet]. 2014 [cited 2017 Dec 2];27:236–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24754245
Petropoulou H, Politis G, Panagakis P, Hatziolou E, Aroni K, Kontochristopoulos G. Immunoglobulin A pemphigus associated with immunoglobulin A gammopathy and lung cancer. J. Dermatol. [Internet]. 2008 [cited 2017 Dec 2];35:341–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18578711
Gonçalves GAP, Brito MMC, Salathiel AM, Ferraz TS, Alves D, Roselino AMF. Incidence of pemphigus vulgaris exceeds that of pemphigus foliaceus in a region where pemphigus foliaceus is endemic: analysis of a 21-year historical series. An Bras Dermatol [Internet]. 2011;86:1109–12. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22281897%5Cnhttp://www.ncbi.nlm.nih.gov/pubmed/2642512
Article
Google Scholar
Mimouni D, Bar H, Gdalevich M, Katzenelson V, David M. Pemphigus, analysis of 155 patients. J Eur Acad Dermatol Venereol. 2010;24:947–52.
CAS
Article
PubMed
Google Scholar
Celere BS, Vernal S, Brochado, MJF, Segura-Muñoz SI, Roselino AM. Geographical foci and epidemiological changes of pemphigus vulgaris in four decades in Southeastern Brazil. Int. J. Dermatol. 2017. p. 1494–6.
Kridin K, Zelber-Sagi S, Khamaisi M, Cohen AD, Bergman R. Remarkable differences in the epidemiology of pemphigus among two ethnic populations in the same geographic region. J Am Acad Dermatol. 2016;75:925–30.
Article
PubMed
Google Scholar
Hahn K, Kippes W, Amagai M, Rzany B, Brocker EB, Zillikens D. Clinical aspects and immunopathology in 48 patients with pemphigus. Hautarzt [Internet]. 2000;51:670–7. Available from: file://o/Referenzmanager/Immunglobulin.PDFs/Hahn2000.pdf
Amin MN, Islam AZMM. Clinical, histologic and immunologic features of pemphigus in Bangladesh. Int J Dermatol. 2006;45:1317–8.
Article
PubMed
Google Scholar
Krain LS. Pemphigus: epidemiologic and survival characteristics of 59 patients, 1955–1973. Arch. Dermatol. [Internet]. American Medical Association; 1974 [cited 2017 Dec 3];110:862. Available from: https://doi.org/10.1001/archderm.1974.01630120012002