2018
DOI: 10.1159/000488902
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Successful Treatment of Pityriasis Rubra Pilaris with Ixekizumab

Abstract: Pityriasis rubra pilaris is an inflammatory dermatologic disorder of unknown cause and often confounded with psoriasis. It is characterised by hyperkeratotic follicular papules, scaly erythematous plaques, palmoplantar keratoderma, and a progression to generalised erythroderma. Here, we report the case of a 68-year-old man with pityriasis rubra pilaris, who was successfully treated with ixekizumab, an interleukin-17A inhibitor.

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Cited by 21 publications
(18 citation statements)
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“…The presence of CARD14 mutations and histopathologic similarities between CAPE, psoriasis, and PRP point to a shared pathogenesis featuring activation of the Th17 pathway, and agents targeting this pathway have efficacy in all three diseases . Recent studies show that other Th17‐activating genodermatoses include various ichthyoses, and trials using similar agents are underway …”
Section: Discussionmentioning
confidence: 99%
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“…The presence of CARD14 mutations and histopathologic similarities between CAPE, psoriasis, and PRP point to a shared pathogenesis featuring activation of the Th17 pathway, and agents targeting this pathway have efficacy in all three diseases . Recent studies show that other Th17‐activating genodermatoses include various ichthyoses, and trials using similar agents are underway …”
Section: Discussionmentioning
confidence: 99%
“…These are canonical pathways implicated in psoriasis. Interestingly, inhibition of the Th17 pathway has now shown therapeutic benefit in psoriasis, PRP, and CAPE . In this study, we discuss histopathologic findings in patients diagnosed as having CAPE.…”
Section: Introductionmentioning
confidence: 96%
“…Not all patients responded to anti-IL-17A, suggesting that further studies are required to evaluate the role of IL-17 in PRP patients. In a recent report on a PRP patient successfully treated with another anti-IL-17A antibody, ixekizumab, Hanfstingl et al 5 referred to the previous paper that clinical improvement was paralleled by a decrease in lesional Th17 cytokines during effective anti-IL-12/IL-23 therapy with ustekinumab, 7,8 and highlighted the IL-23/IL-17 axis in the pathogenesis of PRP. Successful treatments for refractory PRP with ustekinumab have been recently reported.…”
Section: Discussionmentioning
confidence: 99%
“…Our present case progressed to generalized erythroderma after treatment with IL‐17A antibody secukinumab. But there are some reports of successful treatment of PRP with anti‐IL‐17A . Bonomo et al .…”
Section: Discussionmentioning
confidence: 99%
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