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1.
J Laryngol Otol ; 130(1): 8-14, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26585180

RESUMEN

BACKGROUND: This study was undertaken to determine the optimum approach to screening for head and neck cancer based on international experiences. OBJECTIVE: To determine whether or not head and neck cancer is suitable for screening, and, if so, what the ideal approach should be. METHODS: An electronic search of online databases up to and including May 2014 was conducted. Key search terms included 'head and neck', 'cancer', 'screening', 'larynx', 'oropharynx' and 'oral'. RESULTS: Subset analysis of high-risk cohorts showed statistically significant improvements in early detection of head and neck cancer via screening. CONCLUSION: Current levels of public awareness regarding head and neck cancers are suboptimal, despite increased incidence and mortality. Scheduled and opportunistic screening, coupled with efforts to enhance education and health behaviour modification, are highly recommended for pre-defined, high-risk, targeted populations. This can enable early detection and therefore improve morbidity and mortality.


Asunto(s)
Detección Precoz del Cáncer/métodos , Neoplasias de Cabeza y Cuello/prevención & control , Tamizaje Masivo/organización & administración , Salud Global , Humanos , Infecciones por Papillomavirus/prevención & control , Ensayos Clínicos Controlados Aleatorios como Asunto
2.
Ir J Med Sci ; 185(4): 955-957, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25503966

RESUMEN

Diagnosis and interpretation of hereditary breast cancer can be a complex and challenging dilemma. Advances in genetic testing have resulted in guidelines for clinical evaluation and recommendations. Here, we present a case of one family with multiple cases of early-onset breast cancer, some due to a familial BRCA1 mutation but others unrelated to this pathogenic E143X nonsense mutation. In this case report, we highlight the complexities associated with adhering strictly to guidelines and highlight the need for clinical experience in when to deviate from recommended protocols.


Asunto(s)
Neoplasias de la Mama/genética , Codón sin Sentido/genética , Genes BRCA1/fisiología , Adulto , Proteína BRCA1/genética , Neoplasias de la Mama/diagnóstico , Consejo , Femenino , Genes BRCA2/fisiología , Predisposición Genética a la Enfermedad/genética , Pruebas Genéticas/métodos , Humanos , Neoplasias Ováricas/genética , Linaje , Medición de Riesgo/métodos
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