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pityriasis rubra pilaris/eritema
Il collegamento viene salvato negli appunti
Pagina 1 a partire dal 37 risultati
Erythema gyratum repens associated with pityriasis rubra pilaris.
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Erythema gyratum repens (EGR) is a rare cutaneous eruption characterized by serpiginous morphology and a migrating scaly border. It is one of the most specific cutaneous paraneoplastic phenomena, and is associated with malignancy in most cases. We report a 46-year-old Afro-Caribbean man with the
Pityriasis rubra pilaris treated with methotrexate resolving with an erythema gyratum repens-like appearance.
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Resolving classic pityriasis rubra pilaris, mimicker of erythema gyratum repens.
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Erythema gyratum repens, a stage in the resolution of pityriasis rubra pilaris?
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Resolving pityriasis rubra pilaris resembling erythema gyratum repens.
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Transformation from pityriasis rubra pilaris to erythema gyratum repens-like eruption without associated malignancy: A report of 2 cases.
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Response to "Transformation from pityriasis rubra pilaris to erythema gyratum repens-like eruption without associated malignancy: A report of 2 cases".
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Erythema gyratum repens-like eruption after anti-IL-17 therapy of pityriasis rubra pilaris
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Secukinumab monotherapy successfully treated severe refractory type V (atypical juvenile) pityriasis rubra pilaris: a case report and literature review
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Pityriasis rubra pilaris (PRP) is a rare heterogeneous group of papulosquamous inflammatory disorders with unknown etiology. PRP is often resistant to many conventional therapies which has made more challenging on treatment. More recently, several studies have shown encouraging clinical results of
Pityriasis Rubra Pilaris in a 3-Year-Old Male.
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A 3-year-old male presented with progressive pruritic red-orange plaques across most of his body with erythema, desquamation, and fissuring of the hands and feet. He was diagnosed with classic juvenile (type III) pityriasis rubra pilaris (PRP) and treated with oral isotretinoin for 6 months. His
[Pityriasis rubra pilaris].
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Pityriasis rubra pilaris is a rare heterogeneous disorder characterized by follicular keratosis, perifollicular erythema and palmoplantar hyperkeratosis. The aetiology is still unknown. In the majority of cases some triggering factors are found such as trauma or bacterial infection, possibly on a
Erythema elevatum diutinum: a clinicopathological study of eight cases.
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Erythema elevatum diutinum (EED) is a rare cutaneous condition that initially presents as leukocytoclastic vasculitis (LCCV) of the skin and later resolves with fibrosis. In addition to the LCCV, EED may show features reminiscent of other entities. For example, it may mimic lesions of
Pityriasis rubra pilaris response to 13-cis-retinoic acid (isotretinoin).
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Forty-five patients with pityriasis rubra pilaris were treated with oral 13-cis-retinoic acid (isotretinoin). There was marked improvement in the degree of erythema, in duration, and scaling noted within 4 weeks. Remission or maintained improvement persisted after stopping therapy in many of the
Pityriasis rubra pilaris--a retrospective single center analysis over eight years.
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BACKGROUND
Pityriasis rubra pilaris (PRP) is a rare papulosquamous dermatosis. We evaluated evaluate co-morbidities, complications, and outcome of treatment regimens.
METHODS
This is a retrospective study at an academic teaching hospital. We analyzed all patients with the definite diagnosis of PRP
Pityriasis rubra pilaris and celiac sprue with malabsorption.
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A case is reported herein of a young man with pityriasis rubra pilaris, a disease of unknown cause, and malabsorption due to celiac bowel disease. The patient responded to high-dose vitamin A therapy (500,000 IU orally per day for fourteen days). There was complete exfoliation of the palmar-plantar
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