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Risk Reducing Surgery in Carriers with Double Heterozygosity for BRCA1 and BRCA2 Mutations
Journal of Genetic Medicine ; : 25-30, 2012.
Article Dans Anglais | WPRIM | ID: wpr-66744
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.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Tumeurs du sein / Mastectomie partielle / Mastectomie simple / Dépistage génétique / Gène BRCA1 / Assistance / Gène BRCA2 / Tumeurs du rein / Corée / Lymphadénectomie Type d'étude: Etude d'étiologie / Étude pronostique Limites du sujet: Humains Pays comme sujet: Asie langue: Anglais Texte intégral: Journal of Genetic Medicine Année: 2012 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Tumeurs du sein / Mastectomie partielle / Mastectomie simple / Dépistage génétique / Gène BRCA1 / Assistance / Gène BRCA2 / Tumeurs du rein / Corée / Lymphadénectomie Type d'étude: Etude d'étiologie / Étude pronostique Limites du sujet: Humains Pays comme sujet: Asie langue: Anglais Texte intégral: Journal of Genetic Medicine Année: 2012 Type: Article