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Risk Reducing Surgery in Carriers with Double Heterozygosity for BRCA1 and BRCA2 Mutations
Article en En | WPRIM | ID: wpr-66744
Biblioteca responsable: WPRO
ABSTRACT
Among the treatment options for BRCA mutation carriers, risk reducing surgery is the most effective. However, this procedure has been rarely performed in Korea. Interestingly, our case showed double heterozygosity for BRCA1 and BRCA2 mutations. The patient was diagnosed with left renal cancer and left breast cancer at 45-years-of-age, 4 years before risk reducing surgery. The patient received left radical nephrectomy and left partial mastectomy with axillary lymph node dissection. After pretest counseling, the patient underwent genetic testing that identified BRCA1 and BRCA2 mutations. After post-test counseling, the patient decided on intensive surveillance. At 49-years-of-age, the patient was newly diagnosed with contralateral breast cancer. Treatment options were discussed once again. We performed bilateral total mastectomy with immediate reconstruction and prophylactic bilateral salpingo-oophorectomy after multidisciplinary discussion. The patient has been satisfied with the results of surgery. We think this procedure is a recommendable treatment option for BRCA mutation carriers.
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Texto completo: 1 Índice: WPRIM Asunto principal: Neoplasias de la Mama / Mastectomía Segmentaria / Mastectomía Simple / Pruebas Genéticas / Genes BRCA1 / Consejo / Genes BRCA2 / Neoplasias Renales / Corea (Geográfico) / Escisión del Ganglio Linfático Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Journal of Genetic Medicine Año: 2012 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Neoplasias de la Mama / Mastectomía Segmentaria / Mastectomía Simple / Pruebas Genéticas / Genes BRCA1 / Consejo / Genes BRCA2 / Neoplasias Renales / Corea (Geográfico) / Escisión del Ganglio Linfático Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Journal of Genetic Medicine Año: 2012 Tipo del documento: Article