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1.
Eur J Ophthalmol ; 20(6): 1059-65, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20602321

RESUMO

PURPOSE: To determine the efficacy of liquid-based cytology (LBC) and immunohistochemistry in the evaluation of fine needle aspiration biopsy (FNAB) of intraocular melanocytic tumors. METHODS: Cytologic diagnosis was necessary in 25 patients with intraocular melanocytic tumors to deliver a therapeutic course of treatment. The patients' clinical, cytologic, and histologic diagnoses were correlated. All samples were stained with hematoxylin and eosin, and studied through standardized monolayer techniques, with a mean cellular concentration of 60,000 cells/mm2. Immunohistochemistry was performed using Vimentin, S 100, HMB 45, Melan A, cytokeratin, and as prognostic factors, B and T lymphocyte, CD68 (macrophage), and antibody Ki 67 (growth factor). RESULTS: The positive predictive value was 100%; the negative predictive value was 80%. Sensitivity and specificity of LBC for detecting malignancy were 95.2% and 100%, respectively. The FNAB LBC with immunohistochemistry findings resulted in a revision of treatment in 32% of patients. There was no evidence of local tumor dissemination or a recurrence associated with biopsy in any patient. CONCLUSIONS: Fine needle aspiration biopsy (LBC and immunohistochemistry) is a safe, sensitive, and specific method of establishing tissue diagnosis in a subset of patients with intraocular melanocytic tumors, particularly in cases where sample material is scarce. The routine use of immunohistochemical stain increases the diagnostic utility, and prognosis factor determination may change clinical management.


Assuntos
Biópsia por Agulha Fina , Síndrome do Nevo Displásico/diagnóstico , Imuno-Histoquímica , Melanoma/diagnóstico , Nevo Pigmentado/diagnóstico , Neoplasias Uveais/diagnóstico , Adulto , Idoso , Biomarcadores Tumorais/análise , Técnicas Citológicas , Síndrome do Nevo Displásico/metabolismo , Síndrome do Nevo Displásico/cirurgia , Enucleação Ocular , Reações Falso-Positivas , Feminino , Humanos , Iridectomia , Masculino , Melanoma/química , Melanoma/cirurgia , Pessoa de Meia-Idade , Proteínas de Neoplasias/análise , Nevo Pigmentado/química , Nevo Pigmentado/cirurgia , Valor Preditivo dos Testes , Estudos Prospectivos , Sensibilidade e Especificidade , Neoplasias Uveais/química , Neoplasias Uveais/cirurgia , Adulto Jovem
2.
J Invest Dermatol ; 104(3): 340-4, 1995 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-7860998

RESUMO

High levels of cytosolic cathepsin D expression have been associated with poor prognosis in breast cancer node-negative patients. In this work, we provide evidence that three cell lines established from human metastatic melanomas--IIB-MEL-J, IIB-MEL-LES, and IIB-MEL-IAN--express high levels of procathepsin D mRNA. IIB-MEL-J cells secreted into the conditioned media about 30% of the newly synthesized protein, which was active at acidic pH. Melanoma tumors arising in nude mice after injection of the three different cell lines expressed high levels of procathepsin D mRNA. Moreover, 13 human metastatic melanomas expressed variable levels of procathepsin D mRNA. To study the possible association between cathepsin D expression and melanoma development, samples corresponding to 10 primary tumors, 11 metastatic melanomas, 10 dysplastic nevi, 27 nevocellular nevi, and normal melanocytes were studied by immunohistochemistry for cathepsin D-specific staining. We found that cathepsin D was expressed in all of the dysplastic nevi and primary and metastatic melanomas tested but in only 18% of nevocellular nevi (five of 27), whereas normal melanocytes showed no cathepsin D expression. The overall data indicate that cathepsin D is expressed at a high level by melanoma cells, and because of its expression in preneoplastic lesions, it may be associated with melanoma development.


Assuntos
Catepsina D/análise , Síndrome do Nevo Displásico/metabolismo , Melanoma/secundário , Catepsina D/genética , Catepsina D/metabolismo , Meios de Cultivo Condicionados , Expressão Gênica , Humanos , Imuno-Histoquímica , Melanoma/química , Melanoma/genética , RNA Mensageiro/análise , Células Tumorais Cultivadas
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