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2.
Lasers Med Sci ; 39(1): 53, 2024 Jan 31.
Artigo em Inglês | MEDLINE | ID: mdl-38291288

RESUMO

Lichen sclerosus (LS) is a chronic inflammatory dermatosis typical of the genital region, with rare involvement of extragenital areas and particularly the face. LS therapeutic management is challenging, and common therapies including topical and systemic corticosteroids, topical calcineurin inhibitors, surgery are often ineffective. Herein, we present a case of LS occurred in a 36-year-old girl with facial involvement resistant to therapy with systemic corticosteroids and topical tacrolimus. Considering the involvement of a sensitive area, the young age of the patient, and the consistent clinical experience in using photodynamic therapy for the treatment of facial skin disease, we started a treatment with topical 5-aminolevulinic acid (ALA)-photodynamic therapy (PDT) with a dosage of 37 J/cm2 once a month. We compared our case with eight other facial LS patients from the literature and treated differently.


Assuntos
Líquen Escleroso e Atrófico , Fotoquimioterapia , Líquen Escleroso Vulvar , Feminino , Humanos , Adulto , Líquen Escleroso e Atrófico/tratamento farmacológico , Ácido Aminolevulínico/uso terapêutico , Líquen Escleroso Vulvar/tratamento farmacológico , Doença Crônica , Corticosteroides/uso terapêutico , Fármacos Fotossensibilizantes/uso terapêutico
8.
Skin Appendage Disord ; 7(2): 115-119, 2021 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-33796557

RESUMO

Acne fulminans (AF) is a rare, acute, and severe form of acne vulgaris often associated with systemic symptoms. Its treatment is challenging and controversial. We report a case of isotretinoin-induced AF (IIAF) in a 12-year-old boy resistant to traditional therapies (oral steroids and isotretinoin). The patient was successfully treated with adalimumab that can be considered an effective off-label option in the treatment of resistant IIAF in children.

10.
Dermatol Ther ; 33(6): e14223, 2020 11.
Artigo em Inglês | MEDLINE | ID: mdl-32820849

RESUMO

Pityriasis rubra pilaris (PRP) is a rare inflammatory dermatosis characterized by hyperkeratotic follicular papules and erythematous-desquamative plaques that tend to progressively evolve into erythroderma. Treatment is challenging given that international guidelines are not available and large-scale trials do not exist. Traditionally, many topical and systemic drugs had been used as consolidated agents; recently, biologicals are gaining increasing importance, promisingly dominating the therapeutic scenario ahead. Herein, we present a case series showing the "past" and the "future" therapeutic approaches to erythrodermic PRP, one case treated with acitretin and nb-UVB phototherapy combination, while the other with ustekinumab, performing also a throughout literature review.


Assuntos
Fármacos Dermatológicos , Pitiríase Rubra Pilar , Terapia Ultravioleta , Acitretina/uso terapêutico , Fármacos Dermatológicos/uso terapêutico , Humanos , Pitiríase Rubra Pilar/diagnóstico , Pitiríase Rubra Pilar/tratamento farmacológico , Ustekinumab/uso terapêutico
13.
Dermatol Ther (Heidelb) ; 8(3): 491-494, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29855895

RESUMO

Lichen planus (LP) is a chronic inflammatory disease that affects the skin and oral mucosa. Although its etiology is unknown, its potential for cancerization has been confirmed. We herein report the cases of a brother and sister, both with a 15-year history of nail lichen planus of the fingers and toes, who developed squamous cell carcinomas of the nail bed and matrix. This article shows the potential for malignant transformation in lichen planus disease and highlights the importance of periodic clinical follow-up.

14.
Dermatol Ther (Heidelb) ; 7(4): 563-570, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29052100

RESUMO

Acute localized exanthematous pustulosis (ALEP) is a localized form of acute generalized exanthematous pustulosis, characterized by acute onset of multiple nonfollicular, pinhead-sized, sterile pustules following drug administration. Antibiotics, especially ß-lactams and macrolides, have been implicated in the majority of cases, although eruption after nonsteroidal antiinflammatory drugs and many other medications has also been reported. Skin reaction arises quickly within a few hours, resolving rapidly within a few days without treatment, and it is usually accompanied by fever and neutrophilic leukocytosis. We report herein all cases of ALEP described in literature, adding the case of a 35-year-old woman admitted to our hospital with outbreak of erythematous pustules on her face, neck, and chest after amoxicillin-clavulanic acid treatment.

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