472 CARD14 variants in pityriasis rubra pilaris
نویسندگان
چکیده
منابع مشابه
Photosensitive pityriasis rubra pilaris
Pityriasis rubra pilaris (PRP) is a rare, chronic papulosquamous skin disorder. The skin lesions rarely have a predilection to sun-exposed areas although it is known that natural sunlight and phototherapy can exacerbate PRP [1–4]. We present a case of a patient suffering from pityriasis rubra pilaris with photoexposed distribution and photosensitivity exclusively to UVB objectively detected by ...
متن کاملAdult onset pityriasis rubra pilaris.
Pityriasis rubra pilaris (PRP) has always been an intriguing topic ever since its inception. It is a group of chronic disorders characterized by reddish orange plaques with pityriasiform scaling showing follicular keratoses, palmoplantar keratoderma, and sometimes, erythroderma. It occurs all over the world but with racial variations. Its incidence might vary and the age at onset, behavior, cli...
متن کاملLiving with pityriasis rubra pilaris.
Dermatology nurses and other health care professionals may sometimes fail to appreciate and recognize the physical and emotional challenges faced by patients with a particular chronic dermatologic disease or condition. To better bring patients’ feelings and perceptions into focus, the Dermatology Nursing Editorial Board is excited to introduce a new series, “Patients’ Perspectives: Living With....
متن کاملAnalysis of CARD14 Polymorphisms in Pityriasis Rubra Pilaris: Activation of NF-κB
TO THE EDITOR Pityriasis rubra pilaris (PRP) is a rare inflammatory papulosquamous disorder manifesting with palmoplantar keratoderma and follicular hyperkeratotic papules that tend to coalesce into large, scaly, erythematous plaques often progressing to exfoliative erythroderma (Klein et al., 2010; Petrof et al., 2013). PRP is often misdiagnosed as psoriasis, a more common papulosquamous infla...
متن کاملBevacizumab-induced pityriasis rubra pilaris-like eruption.
Pityriasis rubra pilaris is a rare inflammatory disorder characterized by follicular papules on an erythematous base often exhibiting islands of unaffected skin, follicular plugging, and palmoplantar hyperkeratosis. While vitamin A deficiency and autoimmune reactions have been hypothesized as possible etiologies of this condition, pityriasis rubra pilaris-like eruptions secondary to medications...
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ژورنال
عنوان ژورنال: Journal of Investigative Dermatology
سال: 2018
ISSN: 0022-202X
DOI: 10.1016/j.jid.2018.03.479