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1.
An. bras. dermatol ; 93(3): 385-390, May-June 2018. tab, graf
Artigo em Inglês | LILACS | ID: biblio-949872

RESUMO

Abstract: BACKGROUND: Narrow-band UVB (NB-UVB) has been shown to be one of the most effective treatment modalities for psoriasis. Tazarotene, a known effective anti-psoriatic modality, when combined with NB-UVB may enhance the therapeutic success. OBJECTIVE: To study clinical efficacy and safety of combination of NB-UVB with topical tazarotene 0.05% gel in psoriasis. METHOD: Thirty patients with plaque psoriasis having symmetrical lesions were enrolled for 12 weeks. All patients were instructed to apply tazarotene gel on target plaque on left side of body once daily. In addition, the whole body was irradiated with NB-UVB twice weekly. Efficacy was assessed by target plaque scoring and number of treatment sessions for clearance. RESULT: Our study resulted in 3 key findings: Firstly, therapeutic efficacy of NB-UVB was enhanced by addition of tazarotene. This enhanced efficacy was more apparent in decreasing scaling and thickness as compared to decrease in erythema. Secondly, combination therapy showed faster clearance of target plaques, with reduction in mean number of treatment sessions. Thirdly, mean cumulative NB-UVB dose needed to achieve clearance of target plaques was significantly reduced with combination therapy. STUDY LIMITATIONS: The study was not randomized or controlled, but an open-label trial. The study period was relatively short, i.e., 12 weeks, without any follow-up period. CONCLUSION: Tazarotene gel significantly enhances the therapeutic efficacy of NB-UVB irradiation with faster clearance and without serious side effects.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Adulto Jovem , Psoríase/radioterapia , Terapia Ultravioleta/métodos , Seguimentos , Fármacos Dermatológicos/administração & dosagem , Psoríase/tratamento farmacológico , Fatores de Tempo , Estudos Prospectivos , Resultado do Tratamento , Terapia Combinada/métodos , Ácidos Nicotínicos/administração & dosagem
2.
An. bras. dermatol ; 92(6): 801-806, Nov.-Dec. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-887121

RESUMO

Abstract: Background: Narrow-band UVB is the most innovative steroid sparing treatment in atopic dermatitis. There are studies showing efficacy of Narrow-band UVB in childhood atopic dermatitis, but there is lack of clinical trials in the literature determining the length of remission. Therefore, we sought to highlight its efficacy, safety and its post-treatment efficacy in childhood atopic dermatitis. Objective: To assess the clinical efficacy, safety of Narrow-band UVB in the treatment of paediatric atopic dermatitis and length of remission during 2 years of post-treatment follow-up. Methods: Thirty children (4-14 years) having moderate to severe AD (SCORAD index > 25) were enrolled for 12 weeks. Narrow-band UVB phototherapy was administered twice a week on non-consecutive days for three months. SCORAD index was calculated by the same dermatologist at baseline, 6th, 12th, 18th and 24th treatment session. Secondary outcomes were measured using visual analog scale for pruritus and sleep loss. Patients were also followed-up for 2 years to know the length of remission after end of therapy. Results: There was a significant reduction in SCORAD index at 6th, 12th, 18th and 24th treatment session in comparison to baseline. This improvement in SCORAD was also maintained during the 2 years of post-treatment follow-up period. Consequently, pruritus and sleep loss improved significantly from baseline to end of therapy and even during the 1st and 2nd year of follow-up. Study limitation: Open-label trial without control group. Conclusions: Narrow-band UVB is an efficacious and safe modality of treatment in childhood atopic dermatitis with good therapeutic index and minimal side effects.


Assuntos
Humanos , Masculino , Pré-Escolar , Criança , Adolescente , Terapia Ultravioleta/métodos , Dermatite Atópica/radioterapia , Prurido/radioterapia , Fatores de Tempo , Índice de Gravidade de Doença , Estudos Prospectivos , Reprodutibilidade dos Testes , Análise de Variância , Seguimentos , Resultado do Tratamento , Escala Visual Analógica
3.
An. bras. dermatol ; 92(5): 714-716, Sept.-Oct. 2017. graf
Artigo em Inglês | LILACS | ID: biblio-887050

RESUMO

Abstract: Dyshidrosiform pemphigoid is an acquired autoimmune variant of bullous pemphigoid with persistent vesicobullous eruptions localized on the palms or soles, or both. It generally occurs in the elderly and is rarely reported in childhood. Hereby, we describe the first case of dyshidrosiform pemphigoid in a 12-year-old child, which was limited to the dorsal hands and treated successfully with dapsone (diaminodiphenyl sulfone). Along with this report, we also review the clinical features of various types of dyshidrosiform pemphigoid.


Assuntos
Humanos , Masculino , Criança , Penfigoide Bolhoso/diagnóstico , Mãos , Dermatoses da Mão/diagnóstico , Penfigoide Bolhoso/patologia , Penfigoide Bolhoso/tratamento farmacológico , Dapsona/uso terapêutico , Dermatoses da Mão/patologia , Dermatoses da Mão/tratamento farmacológico , Anti-Infecciosos/uso terapêutico
5.
Indian J Dermatol Venereol Leprol ; 2016 Nov-Dec; 82(6): 695-697
Artigo em Inglês | IMSEAR | ID: sea-178512
6.
Indian J Dermatol Venereol Leprol ; 2010 Sept-Oct; 76(5): 533-537
Artigo em Inglês | IMSEAR | ID: sea-140688

RESUMO

Background: Psoralen UV-A (PUVA) is an established therapy for psoriasis, but there is a well-documenated risk of melanoma and nonmelanoma skin cancer. Narrow-band Ultraviolet-B (NBUVB) therapy has a lower carcinogenic risk, has equal therapeutic potential and is considerably safe in the long term than PUVA. Aim: The aim of present study was to compare the efficacy and side-effects of PUVA and NBUVB in chronic plaque psoriasis. Methods: Sixty patients of chronic plaque psoriasis were taken up for the study and were randomly divided into two groups of 30 each. They were well matched in terms of age, sex, psoriasis extent and pretreatment psoriasis area severity index (PASI) scoring. One group was treated with twice-weekly narrow-band UV-B (TL-01) phototherapy and the other group received twice-weekly oral 8-Methoxsalen PUVA for a period of 3 months. Results: Both the groups achieved >75% reduction in the PASI score or complete clearance at the end of 3 months, but PUVA group patients required significantly fewer number of treatment sessions and fewer number of days to clear the psoriasis as compared to the NBUVB group, while the mean cumulative clearance dose and adverse effects were significantly lower in the NBUVB group. Conclusion: We concluded that PUVA group patients achieved a faster clearance, but the adverse effects were significantly lower in the NBUVB group.

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