Pustular Psoriasis: From Pathophysiology to Treatment

被引:51
作者
Genovese, Giovanni [1 ,2 ]
Moltrasio, Chiara [1 ,3 ]
Cassano, Nicoletta [4 ]
Maronese, Carlo Alberto [1 ,2 ]
Vena, Gino Antonio [4 ]
Marzano, Angelo Valerio [1 ]
机构
[1] Fdn IRCCS Ca Granda, Dermatol Unit, Osped Maggiore Policlin, I-20122 Milan, Italy
[2] Univ Milan, Dept Pathophysiol & Transplantat, I-20122 Milan, Italy
[3] Univ Trieste, Dept Med Surg & Hlth Sci, I-34137 Trieste, Italy
[4] Dermatol & Venereol Private Practice, I-76121 Barletta, Italy
关键词
pustular psoriasis; generalized pustular psoriasis; palmoplantar pustular psoriasis; palmoplantar pustulosis; impetigo herpetiformis; acrodermatitis continua of Hallopeau; clinical features; pathogenesis; therapy; GENERALIZED EXANTHEMATOUS PUSTULOSIS; PALMOPLANTAR PUSTULOSIS; ACRODERMATITIS CONTINUA; IMPETIGO HERPETIFORMIS; JAPANESE PATIENTS; PLAQUE PSORIASIS; AP1S3; MUTATIONS; OPEN-LABEL; IL36RN; EFFICACY;
D O I
10.3390/biomedicines9121746
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pustular psoriasis (PP) is a clinicopathological entity encompassing different variants, i.e., acute generalized PP (GPP), PP of pregnancy (impetigo herpetiformis), annular (and circinate) PP, infantile/juvenile PP, palmoplantar PP/palmoplantar pustulosis, and acrodermatitis continua of Hallopeau (ACH), which have in common an eruption of superficial sterile pustules on an erythematous base. Unlike psoriasis vulgaris, in which a key role is played by the adaptive immune system and interleukin (IL)-17/IL-23 axis, PP seems to be characterized by an intense inflammatory response resulting from innate immunity hyperactivation, with prominent involvement of the IL-36 axis. Some nosological aspects of PP are still controversial and debated. Moreover, owing to the rarity and heterogeneity of PP forms, data on prognosis and therapeutic management are limited. Recent progresses in the identification of genetic mutations and immunological mechanisms have promoted a better understanding of PP pathogenesis and might have important consequences on diagnostic refinement and treatment. In this narrative review, current findings in the pathogenesis, classification, clinical features, and therapeutic management of PP are briefly discussed.
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