Efficacy of cyclosporin soft gelatin capsule for severe psoriasis vulgaris, pustular psoriasis and arthropathy psoriasis.

1991 ◽  
Vol 53 (4) ◽  
pp. 824-829 ◽  
Author(s):  
RYOICHI KAMIDE
2006 ◽  
Vol 8 (2) ◽  
pp. 36
Author(s):  
Montaner SG Julio ◽  
Malte Schutz ◽  
Robert Schwartz ◽  
Dushyantha T Jayaweera ◽  
Alfred F Burnside ◽  
...  

2015 ◽  
Vol 7 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Chiharu Tominaga ◽  
Masaaki Yamamoto ◽  
Yasutomo Imai ◽  
Kiyofumi Yamanishi

A 78-year-old woman who had been suffering from psoriasis vulgaris for 31 years was admitted to hospital because of her erythroderma. A toxic eruption was suspected and she was treated with prednisolone 30 mg daily. However, it was ineffective and, suspecting psoriatic erythroderma, cyclosporine 150 mg daily was administered with tapering of the prednisolone. Two weeks after a dose reduction of cyclosporine to 100 mg/day, erythroderma with widespread generalized pustules and fever developed. Histology of a biopsy revealed inflammatory infiltrates in the skin with a spongiform pustule of Kogoj, which was consistent with generalized pustular psoriasis (GPP). Her pustules improved with additional etretinate 20 mg/day, but the erythroderma persisted and she consulted us. Three sessions of granulocyte and monocyte apheresis once weekly were effective for her condition and decreased her serum levels of IL-6 and IL-8. She had homozygous mutations of c.[28C>T] in IL36RN which cause p.[Arg10Ter]. She is the oldest reported case of GPP with a deficiency of interleukin-36 receptor antagonist (DITRA), although GPP in DITRA has been suggested to usually occur in younger cases with no pre-existing psoriasis vulgaris.


2016 ◽  
Vol 96 (1) ◽  
pp. 120-121 ◽  
Author(s):  
Y Fujimura ◽  
K Natsuga ◽  
Y Hamade ◽  
Y Nomura ◽  
Y Kaku ◽  
...  

2012 ◽  
Vol 4 (5) ◽  
pp. 98 ◽  
Author(s):  
A Patel ◽  
A Lodha ◽  
J Chaudhuri ◽  
P Jadia ◽  
T Joshi ◽  
...  

Biomedicines ◽  
2021 ◽  
Vol 9 (12) ◽  
pp. 1746
Author(s):  
Giovanni Genovese ◽  
Chiara Moltrasio ◽  
Nicoletta Cassano ◽  
Carlo Alberto Maronese ◽  
Gino Antonio Vena ◽  
...  

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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