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7.
Dermatol Ther ; 24(1): 144-7, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21276169

RESUMO

Chondrodermatitis nodularis chronica helicis (CNCH) is a fairly frequent disorder of unknown etiology. Although the elective therapy is surgery, local application of topical steroids, antibiotic ointments, intralesional injection of collagen, cryotherapy, curettage followed by diathermy, and CO(2) laser treatment have also been proposed. The aim of the study was to test the utility of photodynamic therapy (PDT) for CNCH. Two patients with painful CNCH underwent PDT with a 635 nm light source for 20 minutes (70 J/cm(2) ) after application of cream containing 20% 5-aminolevulinic acid (5-ALA) and occlusion for 3 hours. The lesions decreased considerably in size and pain ceased within a few weeks. The results suggest that this method can be useful for treating CNCH, especially in patients with contraindications for surgery.


Assuntos
Doenças das Cartilagens/terapia , Otite Externa/terapia , Fotoquimioterapia/métodos , Idoso , Ácido Aminolevulínico/uso terapêutico , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Manejo da Dor , Resultado do Tratamento
9.
J Eur Acad Dermatol Venereol ; 17(1): 28-33, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12602964

RESUMO

BACKGROUND: The term 'common mole', often used to describe a subset of benign pigmented skin lesions, is traditionally defined on the basis of morpho-chromatic features. In recent years, certain research groups have developed equipment and methods, such as digital dermoscopy analysis, that enable objective evaluation of pigmented skin lesions. OBJECTIVE: In this study we use a digital dermoscopy analyser trained for the recognition of pigmented skin lesions to compare the subjective definition of 'common' and the mathematical concept of 'close to the mean of measurements'. METHODS: A subset (100) of digital images of flat pigmented lesions, obtained in daily practice, were classified by trained and non-expert clinicians as common moles (60) or clear-cut melanoma (40), and processed with a DB-Mips analyser. The resulting parameters, validated by a classifier, were used to evaluate Hotelling's T2 multivariate distances from the mean. RESULTS: 'Common' moles could not be clearly defined in terms of closeness to the means of objectively evaluated parameters. Their diagnosis indudes many other evaluations and clusters of variables. CONCLUSION: The clinical semantics of the term 'common' does not conform to any unambiguous mathematical definition.


Assuntos
Melanoma/patologia , Nevo/patologia , Neoplasias Cutâneas/patologia , Diagnóstico por Computador , Análise Discriminante , Humanos , Medições Luminescentes , Pele/patologia
10.
J Eur Acad Dermatol Venereol ; 17(6): 680-3, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-14761136

RESUMO

BACKGROUND: Cutaneous photoageing is a complex biological process affecting all layers of the skin. Skin damage resulting from intrinsic ageing and extrinsic photoageing may trigger skin cancer. In patients with advanced photoageing and/or diffuse actinic damage, local therapy is often inadequate and the possibility of combined therapy needs to be assessed. SUBJECTS: Here we report three cases of patients over 75 years of age with advanced diffuse epithelial skin damage of photoexposed areas consisting of several superficial actinic keratoses, ipermelanotic lesions and multiple skin cancers. METHODS: Neoplastic lesions and damaged skin were removed by superficial erbium laser ablation and the epidermis reconstructed with autologous epidermal sheets expanded in vitro from healthy cells obtained from unexposed areas of the body. RESULTS: Our initial studies show that this procedure is very effective in the short term for treating and preventing the UV-induced skin cancer and precancerous lesions, and also suggest good long-term control of the disease with very interesting aesthetic results.


Assuntos
Terapia a Laser/métodos , Envelhecimento da Pele/patologia , Transplante de Pele/métodos , Luz Solar/efeitos adversos , Raios Ultravioleta/efeitos adversos , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Terapia Combinada , Epitélio/patologia , Epitélio/efeitos da radiação , Feminino , Seguimentos , Humanos , Masculino , Medição de Risco , Estudos de Amostragem , Índice de Gravidade de Doença , Neoplasias Cutâneas/patologia , Neoplasias Cutâneas/prevenção & controle , Neoplasias Cutâneas/cirurgia
12.
Melanoma Res ; 11(1): 37-44, 2001 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11254114

RESUMO

Epiluminescence light microscopy (ELM) has proven useful in the diagnosis of pigmented skin lesions (PSLs). However, in some cases this technique does not sufficiently increase the diagnostic accuracy in distinguishing pigmented Spitz naevi (PSNs) from melanoma. With the aim of obviating these problems of qualitative interpretation, methods based on the mathematical analysis of PSLs, such as digital dermoscopy analysis (DDA), have recently been developed. In the present study we used a digital dermoscope (DBDermo-MIPS, Dell'Eva-Burroni) to analyse PSNs and melanomas with similar clinical and dermoscopic features for any correlation between variables and to determine its discriminating power with respect to histological diagnosis. The 100 lesions underwent histological examination by three experienced dermatopathologists and were identified as PSNs (43) or melanomas (57). Thirty-six parameters were identified as possible discriminating variables and were grouped in four categories: geometry, colour, texture, and islands of colour. Statistical analysis was used to identify the variables with the highest discriminating power. Stepwise discriminant analysis selected only four variables: entropy, minimum diameter, red lesion value and peripheral dark (the means of these variables were higher in melanomas than in PSNs). Thus the combined use of digital dermoscopy and stepwise logistic discriminant analysis made it possible to single out the best objective variables for distinguishing PSN and melanoma.


Assuntos
Dermatologia/métodos , Melanoma/diagnóstico , Melanoma/patologia , Microscopia/métodos , Nevo de Células Epitelioides e Fusiformes/diagnóstico , Neoplasias Cutâneas/diagnóstico , Dermatologia/instrumentação , Humanos , Modelos Logísticos , Microscopia/instrumentação , Modelos Teóricos , Curva ROC , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Neoplasias Cutâneas/patologia , Software
13.
Arch Dermatol ; 135(12): 1459-65, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10606050

RESUMO

OBJECTIVES: To use a digital dermoscopy analyzer with a series of "borderline" pigmentary skin lesions (ie, clinically atypical nevi and early melanoma) to find correlation between the studied variables and to determine their discriminating power with respect to histological diagnosis. DESIGN: A total of 147 pigmentary skin lesions were histologically examined by 3 experienced dermatopathologists and identified as nevi (n = 90) and melanomas (n = 57). The system evaluated 36 variables to be studied as possible discriminant variables, grouped into 4 categories: geometries, colors, textures, and islands of color. SETTING: University medical department. PATIENTS: A sample of patients with excised pigmentary skin lesions (nevi and melanomas). MAIN OUTCOME MEASURES: Sensitivity, specificity, and accuracy of the model for evaluating "borderline" pigmentary skin lesions. RESULTS: After multivariate stepwise discriminant analysis, only 13 variables were selected to compute the canonical discriminant function. CONCLUSION: The present method made it possible to determine which objective variables are important for distinguishing atypical benign pigmentary skin lesions and early melanoma.


Assuntos
Endoscópios , Processamento de Imagem Assistida por Computador/instrumentação , Melanoma/diagnóstico , Nevo Pigmentado/diagnóstico , Neoplasias Cutâneas/diagnóstico , Adulto , Idoso , Diagnóstico Diferencial , Feminino , Humanos , Aumento da Imagem/instrumentação , Masculino , Melanoma/patologia , Pessoa de Meia-Idade , Nevo Pigmentado/patologia , Sensibilidade e Especificidade , Pele/patologia , Neoplasias Cutâneas/patologia
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