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1.
Arch Dermatol ; 147(10): 1191-5, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22006136

RESUMO

OBJECTIVE: To determine the efficacy of imiquimod cream, 5%, in the treatment of lentigo maligna (LM). DESIGN: Open-label before-and-after interventional study. SETTING: A multidisciplinary melanoma clinic at a major tertiary hospital. PATIENTS: Forty-three patients with biopsy-proven LM of greater than 5 mm in diameter completed this study. INTERVENTIONS: Imiquimod cream, 5%, was applied to the lesion 5 days a week for 12 weeks. The original lesion was excised with a 5-mm margin. MAIN OUTCOME MEASURES: The primary outcome was histopathologic evidence of LM in the excision specimen assessed independently by 2 of 3 dermatopathologists. Visible inflammation during treatment and macroscopic clearance were recorded. RESULTS: When 5 of the 43 patients with discordant histopathologic assessment of the excision specimen were excluded, 20 of 38 patients (53% [95% confidence interval, 36%-69%]) demonstrated histopathologic clearance of LM after imiquimod treatment. Visible inflammation was significantly associated with histopathologic clearance (P = .04), but the positive predictive value was low (62%). Macroscopic clearance showed some association with histopathologic clearance (P = .11). Dermatopathologist concordance for all 43 specimens was substantial (κ = 0.77; 95% confidence interval, 0.57-0.96). CONCLUSIONS: Imiquimod cream, 5%, has limited efficacy in the treatment of LM when determined by histopathologic assessment of the entire treated area. The clinical signs of visible inflammation during treatment and apparent lesion clearance cannot be relied on to assess efficacy.


Assuntos
Aminoquinolinas/uso terapêutico , Antineoplásicos/uso terapêutico , Sarda Melanótica de Hutchinson/tratamento farmacológico , Neoplasias Cutâneas/tratamento farmacológico , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Terapia Combinada , Emolientes/uso terapêutico , Feminino , Humanos , Sarda Melanótica de Hutchinson/cirurgia , Imiquimode , Masculino , Pessoa de Meia-Idade , Neoplasias Cutâneas/cirurgia , Resultado do Tratamento , Adulto Jovem
3.
Contact Dermatitis ; 59(3): 157-64, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18759896

RESUMO

BACKGROUND: The occupational contact dermatitis disease severity index (ODDI) was designed to assess the severity and importantly the functional disability caused by occupational contact dermatitis (OCD) of the hands in patients attending our occupational dermatology clinic. OBJECTIVES: To investigate the accuracy of the ODDI. PATIENTS/METHODS: Of 205 patients, 95 were assessed as having OCD of the hands. Content validity was assessed by content mapping and expert opinion. Construct validity was examined through comparing the ODDI against global clinical dermatology severity assessment (GCDSA). Intraobserver reliability, interobserver reliability, internal consistency, acceptability and convenience were also assessed. RESULTS: The ODDI was found to have content validity by the experts and was moderately correlated with GCDSA, supporting construct validity (Pearson's r = 0.54; P < or = 0.01). The ODDI was shown to be reliable with substantial agreement for both intraobserver reliability [intraclass correlation coefficient (ICC) = 0.62] and interobserver reliability (ICC = 0.75). Internal consistency within the ODDI was almost perfect (ICC = 0.94-0.99) and user survey showed the ODDI to be acceptable, easy and quick to use. CONCLUSIONS: The ODDI is a valid and reliable instrument to assess the severity and functional limitations caused by OCD, in patients who have had treatment or modified work duties, associated with some improvement of their dermatitis.


Assuntos
Dermatite de Contato/classificação , Dermatite de Contato/diagnóstico , Dermatite Ocupacional/diagnóstico , Dermatoses da Mão/diagnóstico , Índice de Gravidade de Doença , Adulto , Dermatite Ocupacional/classificação , Avaliação da Deficiência , Feminino , Dermatoses da Mão/classificação , Humanos , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Inquéritos e Questionários
4.
Australas J Dermatol ; 47(3): 195-7, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16867003

RESUMO

A 41-year-old HIV-positive man presented with a 2-month history of a generalized pruritic rash, which had started on his feet. Patch testing made a diagnosis of allergic contact dermatitis to the textile dye basic red 46, likely to have been present in his dark-blue-coloured socks. Complete resolution of his symptoms occurred with avoidance of these socks. The patient had developed allergic contact dermatitis with a low CD4 T lymphocyte count of 361 cells/microl (normal range 410-1545 cells/microl). This raised the question of the level of CD4 count necessary for an individual to develop allergic contact dermatitis to an allergen, given its role in delayed hypersensitivity. It was concluded that a low CD4 count as a result of HIV infection does not decrease the ability of an individual to develop allergic contact dermatitis. Whereas the effector role in delayed type 4 hypersensitivity reactions is mediated by CD4 T lymphocytes, in allergic contact dermatitis it appears that CD4 T lymphocytes have the suppressor role, with CD8 T lymphocytes having the effector role.


Assuntos
Compostos Azo/toxicidade , Dermatite Alérgica de Contato/etiologia , Infecções por HIV/complicações , Administração Tópica , Adulto , Antialérgicos/administração & dosagem , Vestuário , Dermatite Alérgica de Contato/diagnóstico , Dermatite Alérgica de Contato/tratamento farmacológico , Humanos , Masculino , Furoato de Mometasona , Pregnadienodiois/administração & dosagem , Resultado do Tratamento
5.
Australas J Dermatol ; 47(2): 130-3, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16637811

RESUMO

A 65-year-old man presented with a 7-month history of eight bleeding periungual lesions on both feet. The clinical diagnosis of multiple pyogenic granulomas was confirmed by histological examination. Historically, the pyogenic granulomas appeared 3 months after commencing 5-fluorouracil chemotherapy for rectal carcinoma, suggesting a possible causative relationship. Chemotherapy was ceased by the supervising oncologist. Resolution occurred after two lesions had been treated with curettage and diathermy, and the remaining lesions with occlusive dressings over Kenacomb ointment (triamcinolone acetonide 0.1%, neomycin sulphate 0.25%, gramicidin 0.025%, nystatin 100,000 U/g) topically twice daily for a period of 3 months.


Assuntos
Antimetabólitos Antineoplásicos/efeitos adversos , Fluoruracila/efeitos adversos , Granuloma Piogênico/diagnóstico , Dermatopatias/diagnóstico , Adenocarcinoma/tratamento farmacológico , Adenocarcinoma/patologia , Idoso , Antimetabólitos Antineoplásicos/administração & dosagem , Diagnóstico Diferencial , Fluoruracila/administração & dosagem , Granuloma Piogênico/induzido quimicamente , Granuloma Piogênico/patologia , Humanos , Masculino , Neoplasias Retais/tratamento farmacológico , Neoplasias Retais/patologia , Dermatopatias/induzido quimicamente , Dermatopatias/patologia , Dedos do Pé/patologia
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