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1.
J Am Acad Dermatol ; 84(5): 1278-1284, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33010323

RESUMO

BACKGROUND: No long-term maintenance therapy has been tested in patients with seborrheic dermatitis (SD). OBJECTIVE: We sought to compare the efficacy and tolerance of tacrolimus 0.1% ointment versus ciclopiroxolamine 1% cream as maintenance therapy for severe SD. METHODS: This double-blind randomized controlled study was conducted from 2014 to 2017 in 5 Dermatology Departments and 15 dermatology practices in France. Consecutive patients with severe and chronic facial SD were included. Patients were initially treated with desonide 0.05% cream twice daily for 7 days. Patients cleared after this open phase were randomized to receive tacrolimus 0.1% or ciclopiroxolamine 1% cream 2 times a week 24 weeks. The primary endpoint was disease-free-duration, defined as the time from randomization to first relapse. RESULTS: One hundred fourteen patients were randomized (tacrolimus, n = 57; ciclopiroxolamine, n = 57). Twelve patients relapsed in the tacrolimus group after a median delay of 91.5 days (range 15-195 days) versus 23 patients in the ciclopiroxolamine group (median delay, 27 days [range 13-201 days]). Comparison of disease-free duration curves showed that patients in the tacrolimus group had a longer duration of complete remission than those in the ciclopiroxolamine group (P = .018), corresponding to a hazard ratio of relapse of 0.44 (95% confidence interval 0.22-0.89; P = .022). LIMITATIONS: The theoretical sample size was not reached. CONCLUSION: Tacrolimus 0.1% is more effective than ciclopiroxolamine 1% as maintenance therapy for patients with facial SD.


Assuntos
Ciclopirox/administração & dosagem , Dermatite Seborreica/tratamento farmacológico , Dermatoses Faciais/tratamento farmacológico , Quimioterapia de Manutenção/métodos , Tacrolimo/administração & dosagem , Adulto , Dermatite Seborreica/diagnóstico , Método Duplo-Cego , Esquema de Medicação , Dermatoses Faciais/diagnóstico , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Resultado do Tratamento
2.
Arch Dermatol ; 144(2): 167-71, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18283173

RESUMO

UNLABELLED: Objectives To describe the clinical features of cutaneous and ocular manifestations of childhood rosacea, to propose diagnostic criteria, and to emphasize the possible severity of ocular complications in this age group. DESIGN: Retrospective study. SETTING: Tertiary referral center. Patients Children aged 1 to 15 years who had received a diagnosis of cutaneous and/or ocular rosacea and were seen between January 1, 1996, and December 31, 2005. RESULTS: Of 20 patients, 11 had ocular and cutaneous rosacea, 6 had isolated cutaneous involvement, and 3 had isolated ocular involvement. Dermatologic examination results were sufficient to diagnose rosacea in 12 of the patients (60%). The most common presentation was a papulopustular eruption on a telangiectatic background. In 11 patients (55%), ocular involvement preceded the skin eruption. Among the ophthalmologic manifestations, chalazions and blepharoconjunctivitis were the main presenting symptoms; keratitis was observed in 4 patients and corneal ulcers in 2. Ten patients were treated with oral metronidazole. Intermittent treatment for at least 3 months was used to avoid neurologic toxic effects and to achieve complete remission. Conclusion Although rare, childhood rosacea should be recognized because of the possible severity of ocular involvement.


Assuntos
Oftalmopatias/etiologia , Rosácea/complicações , Rosácea/patologia , Adolescente , Blefarite/etiologia , Calázio/etiologia , Criança , Pré-Escolar , Conjuntivite/etiologia , Úlcera da Córnea/etiologia , Feminino , Humanos , Lactente , Ceratite/etiologia , Masculino , Metronidazol/uso terapêutico , Estudos Retrospectivos , Rosácea/diagnóstico , Rosácea/tratamento farmacológico , Telangiectasia/etiologia , Resultado do Tratamento
3.
Pediatr Dermatol ; 24(3): 280-4, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17542881

RESUMO

Infantile digital fibromatosis is a rare benign fibromatous tumor characterized by both its location on fingers and toes and its distinctive light microscopic appearance. However, treatment modalities are not yet standardized. Surgical excision had been preferred in the past but has the disadvantage of a high recurrence rate. More recently, isolated instances of spontaneous regression have been reported with a short follow-up. We report four children with infantile digital fibromatosis, who underwent spontaneous regression after clinical monitoring and long-term follow-up. We recommend regular follow-up in order to allow for intervention in case of functional impact on the affected extremities.


Assuntos
Fibroma/patologia , Neoplasias Cutâneas/patologia , Criança , Feminino , Fibroma/cirurgia , Dedos , Humanos , Lactente , Masculino , Recidiva , Remissão Espontânea , Neoplasias Cutâneas/cirurgia , Dedos do Pé
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