Zusammenfassung
Eine Reihe pustulöser Hauterkrankungen teilen klinische, pathogenetische und epidemiologische Aspekte mit der Psoriasis vulgaris, und ihre Einordung als eigene klinische Entitäten oder Unterformen der Psoriasis ist weiterhin umstritten, was sich auch in der Vielzahl ihrer Bezeichnungen widerspiegelt. Hierzu gehören die generalisierte pustulöse Psoriasis mit ihren Sonderformen, die Acrodermatitis continua suppurativa, die akute Pustulosis palmoplantaris, die Psoriasis pustulosa palmoplantaris sowie pustulöse Varianten der vorwiegend durch TNF-Blocker getriggerten paradoxen psoriasiformen Dermatitis. In diesem Beitrag werden Erkenntnisse zu Epidemiologie, klinischem Bild, Pathogenese, Genetik und Therapie dieser pustulösen Hauterkrankungen dargestellt.
Abstract
A number of pustular skin diseases share clinical, pathogenetic, and epidemiological aspects with plaque-type psoriasis, and their classification as a separate clinical entity or as a subtype of psoriasis remains controversial, which is also reflected in the multitude of their names. They include generalized pustular psoriasis with its subtypes, acrodermatitis continua suppurativa (Hallopeau), acute pustulosis palmopantaris, palmoplantar pustular psoriasis, and pustular variants of a mostly TNF-blocker triggered paradoxical psoriasiform dermatitis. In this article, the epidemiology, clinical picture, pathogenesis, genetics, and therapy of these pustular skin diseases are described.
Literatur
Capon F (2013) IL36RN mutations in generalized pustular psoriasis: just the tip of the iceberg? J Invest Dermatol 133:2503–2504
Korber A, Mossner R, Renner R et al (2013) Mutations in IL36RN in patients with generalized pustular psoriasis. J Invest Dermatol 133(11):2634–2637
Marrakchi S, Guigue P, Renshaw BR et al (2011) Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis. N Engl J Med 365:620–628
Berki DM, Liu L, Choon SE et al (2015) Activating CARD14 mutations are associated with generalized pustular psoriasis but rarely account for familial recurrence in psoriasis Vulgaris. J Invest Dermatol 135:2964–2970
Brenner M, Molin S, Ruebsam K, Weisenseel P, Ruzicka T, Prinz JC (2009) Generalized pustular psoriasis induced by systemic glucocorticosteroids: four cases and recommendations for treatment. Br J Dermatol 161:964–966
Weisenseel P, Reich K (2013) Paradoxical skin reactions under therapy with TNF-alpha antagonists. Z Rheumatol 72:423–428
Robinson A, Van Voorhees AS, Hsu S, Korman NJ, Lebwohl MG, Bebo BF, Jr., Kalb RE (2012) Treatment of pustular psoriasis: from the Medical Board of the National Psoriasis Foundation. J Am Acad Dermatol 67:279-288 (2012)
Imafuku S, Honma M, Okubo Y et al (2016) Efficacy and safety of secukinumab in patients with generalized pustular psoriasis: A 52-week analysis from phase III open-label multicenter Japanese study. J Dermatol : doi:/10.1111/1346-8138.13306
Saeki H, Nakagawa H, Ishii T et al (2015) Efficacy and safety of open-label ixekizumab treatment in Japanese patients with moderate-to-severe plaque psoriasis, erythrodermic psoriasis and generalized pustular psoriasis. J Eur Acad Dermatol Venereol 29:1148–1155
Fujisawa T, Suzuki S, Mizutani Y et al (2015) Granulocyte and monocyte adsorption Apheresis for generalized pustular psoriasis: therapeutic outcomes in three refractory patients. Ther Apher Dial 19:336–341
Huffmeier U, Watzold M, Mohr J et al (2014) Successful therapy with anakinra in a patient with generalized pustular psoriasis carrying IL36RN mutations. Br J Dermatol 170:202–204
Gao QQ, Xi MR, Yao Q (2013) Impetigo Herpetiformis during pregnancy: a case report and literature review. Dermatology 226:35–40
Sugiura K, Oiso N, Iinuma S et al (2014) IL36RN mutations underlie impetigo herpetiformis. J Invest Dermatol 134:2472–2474
Liao PB, Rubinson R, Howard R et al (2002) Annular pustular psoriasis–most common form of pustular psoriasis in children: report of three cases and review of the literature. Pediatr Dermatol 19:19–25
Albert A, Hein R, Ring J et al (2007) Erythema annulare centrifugum-like psoriasis cum pustulatione. Hautarzt 58:769–773
Stadler R, Orfanos CE (1981) Erythema anulare centrifugum with pustulation. Successful oral retinoid therapy. Hautarzt 32:564–566
Vocks E, Worret WI, Ring J (2003) Erythema annulare centrifugum-type psoriasis: a particular variant of acute-eruptive psoriasis. J Eur Acad Dermatol Venereol 17:446–448
Lo SA, Brancaccio G, Puca RV et al (2012) Etanercept in the treatment of generalized annular pustular psoriasis. Ann Dermatol 24:233–234
Setta-Kaffetzi N, Simpson MA, Navarini AA et al (2014) AP1S3 mutations are associated with pustular psoriasis and impaired Toll-like receptor 3 trafficking. Am J Hum Genet 94:790–797
Wilsmann-Theis D, Hagemann T, Dederer H et al (2004) Successful treatment of acrodermatitis continua suppurativa with topical tacrolimus 0.1 % ointment. Br J Dermatol 150:1194–1197
Sehgal VN, Verma P, Sharma S et al (2011) Acrodermatitis continua of Hallopeau: evolution of treatment options. Int J Dermatol 50:1195–1211
Bacharach-Buhles M, el-Gammal S, Altmeyer P (1993) The pustular bacterid (Andrews). Are there clinical criteria for differentiating from psoriasis pustulosa palmaris et plantaris? Hautarzt 44:221–224
Burge SM, Ryan TJ (1985) Acute palmoplantar pustulosis. Br J Dermatol 113:77–83
Hellgren L, Mobacken H (1971) Pustulosis palmaris et plantaris. Prevalence, clinical observations and prognosis. Acta Derm Venereol 51:284–288
O’Doherty CJ, MacIntyre C (1985) Palmoplantar pustulosis and smoking. Br Med J (Clin Res Ed) 291:861–864
Enfors W, Molin L (1971) Pustulosis palmaris et plantaris. A follow-up study of a ten-year material. Acta Derm Venereol 51:289–294
Becher G, Jamieson L, Leman J (2015) Palmoplantar pustulosis–a retrospective review of comorbid conditions. J Eur Acad Dermatol Venereol 29:1854–1856
Brunasso AM, Puntoni M, Aberer W et al (2013) Clinical and epidemiological comparison of patients affected by palmoplantar plaque psoriasis and palmoplantar pustulosis: a case series study. Br J Dermatol 168:1243–1251
Farley E, Masrour S, McKey J et al (2009) Palmoplantar psoriasis: a phenotypical and clinical review with introduction of a new quality-of-life assessment tool. J Am Acad Dermatol 60:1024–1031
Michaelsson G, Kristjansson G, Pihl LI et al (2007) Palmoplantar pustulosis and gluten sensitivity: a study of serum antibodies against gliadin and tissue transglutaminase, the duodenal mucosa and effects of gluten-free diet. Br J Dermatol 156:659–666
Benhamou CL, Chamot AM, Kahn MF (1988) Synovitis-acne-pustulosis hyperostosis-osteomyelitis syndrome (SAPHO). A new syndrome among the spondyloarthropathies? Clin Exp Rheumatol 6:109–112
Nguyen MT, Borchers A, Selmi C et al (2012) The SAPHO syndrome. Semin Arthritis Rheum 42:254–265
Yamamoto T (2011) Triggering role of focal infection in the induction of extra-palmoplantar lesions and pustulotic arthro-osteitis associated with palmoplantar pustulosis. Adv Otorhinolaryngol 72:89–92
Weisenseel P, Kuznetsov AV, Ruzicka T et al (2007) Palmoplantar pustulosis is not inevitably associated with antigliadin antibodies. Br J Dermatol 156:1399–1400
Agner T, Sindrup JH, Hoier-Madsen M et al (1989) Thyroid disease in pustulosis palmoplantaris. Br J Dermatol 121:487–491
Eriksson MO, Hagforsen E, Lundin IP et al (1998) Palmoplantar pustulosis: a clinical and immunohistological study. Br J Dermatol 138:390–398
Murakami M, Ohtake T, Horibe Y et al (2010) Acrosyringium is the main site of the vesicle/pustule formation in palmoplantar pustulosis. J Invest Dermatol 130:2010–2016
Uehara M, Ofuji S (1974) The morphogenesis of pustulosis palmaris et plantaris. Arch Dermatol 109:518–520
Murakami M, Hagforsen E, Morhenn V et al (2011) Patients with palmoplantar pustulosis have increased IL-17 and IL-22 levels both in the lesion and serum. Exp Dermatol 20:845–847
Murakami M, Kaneko T, Nakatsuji T et al (2014) Vesicular LL-37 contributes to inflammation of the lesional skin of palmoplantar pustulosis. PLoS ONE 9:e110677
Hagforsen E, Edvinsson M, Nordlind K et al (2002) Expression of nicotinic receptors in the skin of patients with palmoplantar pustulosis. Br J Dermatol 146:383–391
Yoshizaki T, Bandoh N, Ueda S et al (2009) Up-regulation of CC chemokine receptor 6 on tonsillar T cells and its induction by in vitro stimulation with alpha-streptococci in patients with pustulosis palmaris et plantaris. Clin Exp Immunol 157:71–82
Ueda S, Takahara M, Tohtani T et al (2010) Up-regulation of ss1 integrin on tonsillar T cells and its induction by in vitro stimulation with alpha-streptococci in patients with pustulosis Palmaris et Plantaris. J Clin Immunol 30:861–871
Asumalahti K, Ameen M, Suomela S et al (2003) Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis. J Invest Dermatol 120:627–632
Setta-Kaffetzi N, Navarini AA, Patel VM et al (2013) Rare pathogenic variants in IL36RN underlie a spectrum of psoriasis-associated pustular phenotypes. J Invest Dermatol 133:1366–1369
Mossner R, Frambach Y, Wilsmann-Theis D et al (2015) Palmoplantar pustular psoriasis is associated with Missense variants in CARD14, but not with loss-of-function mutations in IL36RN in european patients. J Invest Dermatol 135:2538–2541
Kingo K, Mossner R, Koks S et al (2007) Association analysis of IL19, IL20 and IL24 genes in palmoplantar pustulosis. Br J Dermatol 156:646–652
Wu W, Debbaneh M, Moslehi H et al (2014) Tonsillectomy as a treatment for psoriasis: a review. J Dermatolog Treat 25:482–486
Kragballe K, Larsen FG (1991) A hydrocolloid occlusive dressing plus triamcinolone acetonide cream is superior to clobetasol cream in palmo-plantar pustulosis. Acta Derm Venereol 71:540–542
Marsland AM, Griffiths CE (2001) Treatments for chronic palmoplantar pustular psoriasis. Skin Therapy Lett 6:3–5
Umezawa Y, Nakagawa H, Tamaki K (2015) Phase III clinical study of maxacalcitol ointment in patients with palmoplantar pustulosis: A randomized, double-blind, placebo-controlled trial. J Dermatol 43:288
Muro M, Kawakami H, Matsumoto Y et al (2015) Topical combination therapy with vitamin D and corticosteroid ointment for palmoplantar pustulosis: A prospective, randomized, left-right comparison study. J Dermatolog Treat 27:51
Sevrain M, Richard MA, Barnetche T et al (2014) Treatment for palmoplantar pustular psoriasis: systematic literature review, evidence-based recommendations and expert opinion. J Eur Acad Dermatol Venereol 28(Suppl 5):13–16
Layton AM, Sheehan-Dare R, Cunliffe WJ (1991) A double-blind, placebo-controlled trial of topical PUVA in persistent palmoplantar pustulosis. Br J Dermatol 124:581–584
Marsland AM, Chalmers RJ, Hollis S et al (2006) Interventions for chronic palmoplantar pustulosis. Cochrane Database Syst Rev CD001433: doi:/10.1002/14651858.cd001433.pub2
Lassus A, Geiger JM (1988) Acitretin and etretinate in the treatment of palmoplantar pustulosis: a double-blind comparative trial. Br J Dermatol 119:755–759
Wilken R, Sharma A, Patel F et al (2015) Successful treatment of palmoplantar pustulosis with isotretinoin. Dermatol Online J 21
Reich K, Graff O, Mehta N (2016) Oral alitretinoin treatment in patients with palmoplantar pustulosis inadequately responding to standard topical treatment: a randomised Phase II study. Br J Dermatol : doi:10.1111/bjd.14401
Irla N, Navarini AA, Yawalkar N (2012) Alitretinoin abrogates innate inflammation in palmoplantar pustular psoriasis. Br J Dermatol 167:1170–1174
Adisen E, Tekin O, Gulekon A et al (2009) A retrospective analysis of treatment responses of palmoplantar psoriasis in 114 patients. J Eur Acad Dermatol Venereol 23:814–819
Stanford CW, Kollipara R, Melookaran AM et al (2014) Palmoplantar pustular psoriasis following initiation of a beta-blocker: disease control with low-dose methotrexate. Cutis 94:153–155
Reitamo S, Erkko P, Remitz A et al (1993) Cyclosporine in the treatment of palmoplantar pustulosis. A randomized, double-blind, placebo-controlled study. Arch Dermatol 129:1273–1279
Erkko P, Granlund H, Remitz A et al (1998) Double-blind placebo-controlled study of long-term low-dose cyclosporin in the treatment of palmoplantar pustulosis. Br J Dermatol 139:997–1004
Stander H, Stadelmann A, Luger T et al (2003) Efficacy of fumaric acid ester monotherapy in psoriasis pustulosa palmoplantaris. Br J Dermatol 149:220–222
Bissonnette R, Nigen S, Langley RG et al (2014) Increased expression of IL-17 A and limited involvement of IL-23 in patients with palmo-plantar (PP) pustular psoriasis or PP pustulosis; results from a randomised controlled trial. J Eur Acad Dermatol Venereol 28:1298–1305
Robinson A, Van Voorhees AS, Hsu S et al (2012) Treatment of pustular psoriasis: from the Medical Board of the National Psoriasis Foundation. J Am Acad Dermatol 67:279–288
Bissonnette R, Poulin Y, Bolduc C et al (2008) Etanercept in the treatment of palmoplantar pustulosis. J Drugs Dermatol 7:940–946
Au SC, Goldminz AM, Kim N et al (2013) Investigator-initiated, open-label trial of ustekinumab for the treatment of moderate-to-severe palmoplantar psoriasis. J Dermatolog Treat 24:179–187
Tillack C, Ehmann LM, Friedrich M et al (2014) Anti-TNF antibody-induced psoriasiform skin lesions in patients with inflammatory bowel disease are characterised by interferon-gamma-expressing Th1 cells and IL-17 A/IL-22-expressing Th17 cells and respond to anti-IL-12/IL-23 antibody treatment. Gut 63:567–577
Perez-Zafrilla B, Angel DM, Carmona L (2008) Adverse reactions related to the administration of TNF inhibitors. analysis of a registry of biologic therapy. Reumatol Clin 4:90–95
Navarro R, Dauden E (2014) Clinical management of paradoxical psoriasiform reactions during TNF- alpha therapy. Actas Dermosifiliogr 105:752–761
Collamer AN, Battafarano DF (2010) Psoriatic skin lesions induced by tumor necrosis factor antagonist therapy: clinical features and possible immunopathogenesis. Semin Arthritis Rheum 40:233–240
Shmidt E, Wetter DA, Ferguson SB et al (2012) Psoriasis and palmoplantar pustulosis associated with tumor necrosis factor-alpha inhibitors: the Mayo Clinic experience, 1998 to 2010. J Am Acad Dermatol 67:e179–e185
Palucka AK, Blanck JP, Bennett L et al (2005) Cross-regulation of TNF and IFN-alpha in autoimmune diseases. Proc Natl Acad Sci USA 102:3372–3377
Nestle FO, Conrad C, Tun-Kyi A et al (2005) Plasmacytoid predendritic cells initiate psoriasis through interferon-alpha production. J Exp Med 202:135–143
Friedrich M, Tillack C, Wollenberg A et al (2014) IL-36gamma sustains a proinflammatory self-amplifying loop with IL-17 C in anti-TNF-induced psoriasiform skin lesions of patients with Crohn’s disease. Inflamm Bowel Dis 20:1891–1901
Denadai R, Teixeira FV, Steinwurz F et al (2013) Induction or exacerbation of psoriatic lesions during anti-TNF-alpha therapy for inflammatory bowel disease: a systematic literature review based on 222 cases. J Crohns Colitis 7:517–524
Gregoriou S, Kazakos C, Christofidou E et al (2011) Pustular psoriasis development after initial ustekinumab administration in chronic plaque psoriasis. Eur J Dermatol 21:104–105
Wenk KS, Claros JM, Ehrlich A (2012) Flare of pustular psoriasis after initiating ustekinumab therapy. J Dermatolog Treat 23:212–214
Hay RA, Pan JY (2014) Paradoxical flare of pustular psoriasis triggered by ustekinumab, which responded to adalimumab therapy. Clin Exp Dermatol 39:751–752
Laino L, DiCarlo A (2011) Palmoplantar pustular psoriasis: clinical and video thermographic evaluation before and after topical tacrolimus treatment. Arch Dermatol 147:760
Hayama K, Inadomi T, Fujisawa D et al (2010) A pilot study of medium-dose cyclosporine for the treatment of palmoplantar pustulosis complicated with pustulotic arthro-osteitis. Eur J Dermatol 20:758–762
Wozel G, Vitez L (2008) Palmoplantar pustular psoriasis: successful therapy with efalizumab after non-response to infliximab. Acta Derm Venereol 88:169–170
Morales-Munera C, Vilarrasa E, Puig L (2013) Efficacy of ustekinumab in refractory palmoplantar pustular psoriasis. Br J Dermatol 168:820–824
Gerdes S, Franke J, Domm S et al (2010) Ustekinumab in the treatment of palmoplantar pustulosis. Br J Dermatol 163:1116–1118
Bertelsen T, Kragballe K, Johansen C et al (2014) Efficacy of ustekinumab in palmoplantar pustulosis and palmoplantar pustular psoriasis. Int J Dermatol 53:e464–e466
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P. Weisenseel hat von folgenden Firmen unregelmäßig Honorare und/oder Reisekosten für Berater- und/oder Vortragstätigkeiten erhalten und/oder war an klinischen Studien der folgenden Firmen beteiligt: Abbott/Abbvie, Biogen Idec, Dexcel, Eli Lilly, Galderma, GSK, Janssen-Cilag, Leo Pharma, Medac, MSD (früher Essex), Novartis, Pfizer (früher Wyeth). D. Wilsmann-Theis erhielt Vergütung von Tätigkeiten im Rahmen klinischer Studien, Referenten- oder Beratertätigkeiten oder Reisekostenunterstützung in alphabetischer Reihenfolge von den Firmen Abbvie, Almirall Hermal, Amgen, Biogen IDEC, Celgene, Janssen-Cilag, Leo Pharma, Lilly, Merck Serono, MSD Sharp & Dohme, Novartis Pharma und Pfizer. C. Kahl gibt an, dass kein Interessenkonflikt besteht. K. Reich fungierte als Berater und/oder bezahlter Redner und/oder nahm an klinischen Studien teil, die gesponsert wurden von Abbvie, Amgen, Biogen, Boehringer Ingelheim Pharma, Celgene, Centocor, Covagen, Forward Pharma, GlaxoSmithKline, Janssen-Cilag, Leo, Lilly, Medac, Merck Sharp & Dohme Corp., Novartis, Ocean Pharma, Pfizer, Regeneron, Takeda, UCB Pharma, Xenoport. R. Mössner erhielt Vergütung von Tätigkeiten im Rahmen klinischer Studien, Referenten- oder Beratertätigkeiten oder Reisekostenunterstützung in alphabetischer Reihenfolge von den Firmen Abbvie, Biogen IDEC, Celgene, Janssen-Cilag, Leo Pharma, Lilly, Merck Serono, MSD Sharp & Dohme, Novartis Pharma und Pfizer.
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Weisenseel, P., Wilsmann-Theis, D., Kahl, C. et al. Pustulöse Psoriasis. Hautarzt 67, 445–453 (2016). https://doi.org/10.1007/s00105-016-3804-4
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DOI: https://doi.org/10.1007/s00105-016-3804-4