1996
DOI: 10.1046/j.1365-2133.1996.d01-1114.x
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Pilyriasis rubry pilaris and human immunodeficiency virus infection-type 6 pityriasis rubra pilaris?

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Cited by 35 publications
(30 citation statements)
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“…PRP is a rare papulosquamous disorder of unknown aetiology. It has been associated with impaired cell‐mediated immunity, and familial variants have been linked to genetic mutations relevant to other autoinflammatory skin disorders . Clinical findings include orange/red plaques with follicular hyperkeratosis and characteristic ‘islands of sparing’, palmoplantar hyperkeratosis, and frequent progression to erythroderma with pityriasiform scale…”
Section: Discussionmentioning
confidence: 99%
“…PRP is a rare papulosquamous disorder of unknown aetiology. It has been associated with impaired cell‐mediated immunity, and familial variants have been linked to genetic mutations relevant to other autoinflammatory skin disorders . Clinical findings include orange/red plaques with follicular hyperkeratosis and characteristic ‘islands of sparing’, palmoplantar hyperkeratosis, and frequent progression to erythroderma with pityriasiform scale…”
Section: Discussionmentioning
confidence: 99%
“…Although other entities, such as pityriasis rubra pilaris, lichen spinulosus and HIV-associated occlusion follicular syndrome, have been linked to HIV infection [2,3,4,5,6,7,8], we have not observed any such case, so we consider them rare diseases. There are many diseases that can present as itchy folliculitis in HIV-infected patients and are related to immunosuppression and/or immunorestoration [19].…”
Section: Discussionmentioning
confidence: 71%
“…Several dermatoses with follicular occlusion have been described in HIV-infected patients, including acne vulgaris, drug-induced acneiform eruptions, a special form of pityriasis rubra pilaris, lichen spinulosus and acne inversa (hidradenitis suppurativa) [1,2,3,4,5]. These entities appear isolated or associated with each other in an independent disease named ‘HIV-associated follicular syndrome’ [6,7,8].…”
Section: Introductionmentioning
confidence: 99%
“…In recent years, a type VI PRP associated with HIV infection, characterized by a distinctive triad of nodulocystic acne, lichen spinulosus, and a PRPlike eruption, has been proposed. 6,7 Because of the rarity of the disease, especially in children, large-scale studies of juvenile PRP are limited with diverse conclusions about its manifestation, classification, and treatment. 4,8 Here we report a long-term observational study of 28 juvenile cases in Taiwan.…”
mentioning
confidence: 99%