Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros











Intervalo de ano de publicação
1.
Dermatol. argent ; 17(4): 277-283, jul.-ago.2011. ilus, graf
Artigo em Espanhol | LILACS | ID: lil-724153

RESUMO

Introducción.La vulva puede ser asiento de diversos tumores malignos, de los cuales el más frecuente es el espinocelular; sin embargo, los tumores vulvares no espinocelulares son de gran importancia debido su mal pronóstico.Objetivos. Determinar la forma de presentación clínica, sintomatología, variedad histopatológica y el estadio de los tumores vulvares no espinocelulares al momento de la consulta. Evaluar el rol del dermatólogo en el diagnóstico y seguimiento de estos pacientes. Métodos. Se realizó un estudio retrospectivo, observacional y analítico de pacientes que concurrieron por derivación al consultorio de Patología Vulvar desde agosto de 2002 a agosto de 2010. Se evaluaron las historias clínicas y los archivos anatomopatológicos e iconográficos delos tumores vulvares no espinocelulares. Resultados. De un total de 637 consultas por derivación en el consultorio de patología vulvar, el 9,1% (n=56) correspondió a tumores malignos. De éstos, el 76,78% (n=43) fueron carcinoma espinocelular (incluidos neoplasia intravulvar y carcinoma invasor) y el 23,22% (n=15), carcinoma no espinocelular. Del total de estos últimos, ocuparon en orden de frecuenta decreciente: tumores secundarios de otros órganos, enfermedad de Paget extramamaria, melanoma, adenocarcinoma de la glándula de Bartolino y sarcoma. El motivo de consulta más frecuente fue dolor, y la forma clínica de presentación fue lesión exofítica única. Conclusiones. Destacamos la alta incidencia de tumores vulvares no espinocelulares en nuestro medio: representa el 23,2% de las neoplasias vulvares, en comparación con la literatura, que es del 10%.


Background. The vulva may be the seat of many malignancies, of which the most common is squamous-cell carcinoma; nevertheless non squamous-cell vulvar neoplasms are significant because of their poor prognosis. Objectives. To determine the symptoms, clinical presentation and stage of the disease at thetime of consultation. To establish associations with various risk factors and evaluate prognosis. Toasess the role of the dermatologist in the appropriate diagnosis and monitoring of these patients.Methods. We performed a retrospective and observational study of patients seen at a vulvar-disease Clinic from August 2002 to August 2010. We reviewed the clinical records, biopsy specimens and iconographic files.Results.From a total of 680 consultations to a vulvar-disease Clinic 7% (n=48) corresponded to malignant tumors. Of these 73% (n=35) were squamous-cell carcinomas and 27% (n=13) were non-squamous-cell carcinomas, which in decreasing order of frequency, were: secondarytumors from other organs, extramamammary Paget’s disease, melanoma, adenocarcinoma andsarcoma. The most frequent cause of consultation was pain, and the clinical presentation was a single exophytic lesion.


Assuntos
Feminino , Neoplasias Vulvares/diagnóstico , Neoplasias Vulvares/etiologia , Neoplasias Vulvares/terapia , Glândulas Vestibulares Maiores , Glândulas Vestibulares Maiores/patologia , Melanoma , Doença de Paget Extramamária , Prognóstico , Rabdomiossarcoma
2.
Mol Oncol ; 2(1): 102-11, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19383332

RESUMO

We have analyzed the predictive/prognostic value of Bcl-2 protein in breast cancer patients treated with neoadjuvant chemotherapy. One hundred and ten patients were submitted to two different chemotherapeutic regimens: a) 5-fluorouracil, adriamycin or epirubicin, and cyclophosphamide (FAC/FEC) during 2-6 cycles before surgery and 3 or 4 additional cycles of FAC/FEC after surgery (n=40) and b) doxorubicin (D) 75 mg/m(2) or epirubicin (E) 120 mg/m(2) during 4 cycles before surgery, and 6 cycles of cyclophosphamide, methotrexate, and 5-fluorouracil (CMF) after surgery (n=70). Bcl-2 expression, evaluated by immunohistochemistry, did not change significantly after chemotherapy and was not related to clinical/pathological response. In FAC/FEC group, Bcl-2 positive expression after chemotherapy correlated with better disease free survival (DFS) and overall survival (OS) (P=0.008 and P=0.001). In D/E group, Bcl-2 also correlated with better DFS and OS (P=0.03 and P=0.054) in the post-chemotherapy biopsies. An unusual nuclear localization of Bax was observed in some biopsies, but this localization did not correlate with the tumor response or outcome of the patients. We found that a high Bcl-2 expression had no predictive value but had prognostic value in breast cancer patients treated with neoadjuvant anthracycline based chemotherapy.


Assuntos
Antibióticos Antineoplásicos/uso terapêutico , Neoplasias da Mama/diagnóstico , Neoplasias da Mama/mortalidade , Valor Preditivo dos Testes , Proteínas Proto-Oncogênicas c-bcl-2/análise , Antraciclinas/uso terapêutico , Protocolos de Quimioterapia Combinada Antineoplásica , Neoplasias da Mama/tratamento farmacológico , Feminino , Humanos , Terapia Neoadjuvante/métodos , Prognóstico , Análise de Sobrevida , Resultado do Tratamento , Proteína X Associada a bcl-2/análise
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA