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1.
Am J Dermatopathol ; 38(1): 52-5, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26332533

RESUMO

Giant basal cell carcinomas (GBCCs) are a strange and aggressive variety of basal cell carcinomas (BCCs); they are characterized by deep tissue invasion, rapid growth, high risk of metastasis, and a poor prognosis. GBCCs represent 0.4%-1% of all BCCs. The pathogenesis of GBCC is sometimes linked to a spontaneous mutation in the PTCH gene, mapped to the q22.33 locus of chromosome 9. The key factor in the development of GBCC, in at least 30% of the cases, is the delay in seeking medical attention (7.5 ± 3.1 years). This is associated to a poor socioeconomic level, deficient hygiene, mental illness, advanced age, and the fact that BCCs are painless lesions. The authors present a Mexican female with a 2-year ulcer diagnosed as a GBCC in the year 2000, its initial therapeutic approach, and her follow-up during the next 12 years.


Assuntos
Carcinoma Basocelular/complicações , Neoplasias Faciais/complicações , Recidiva Local de Neoplasia/complicações , Neoplasias Cutâneas/complicações , Úlcera Cutânea/etiologia , Adulto , Carcinoma Basocelular/patologia , Progressão da Doença , Enucleação Ocular , Face , Neoplasias Faciais/patologia , Feminino , Seguimentos , Humanos , Deformidades Adquiridas Nasais/etiologia , Neoplasias Cutâneas/patologia
2.
Rev Gastroenterol Mex ; 71(3): 312-5, 2006.
Artigo em Espanhol | MEDLINE | ID: mdl-17140054

RESUMO

Colorectal cancer is an important neoplasm in general population, about 90% of the cases are sporadical, but near of 5% are due to hereditary non polyposis colorectal cancer. Early detection is imperative due to genetic linkage and association to other neoplasms diagnosed an early age. This case report is about a young man diagnosed with colorectal cancer that presented multiple recurrences and had at least two affected generations. The most important aspects of diagnosis, management and genetic counseling are discussed.


Assuntos
Neoplasias Colorretais Hereditárias sem Polipose/genética , Neoplasias Colorretais Hereditárias sem Polipose/diagnóstico , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem
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