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Risk Reducing Surgery in Carriers with Double Heterozygosity for BRCA1 and BRCA2 Mutations

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dc.contributor.authorHong, WS-
dc.contributor.authorKim, KS-
dc.contributor.authorJung, YS-
dc.contributor.authorKang, SY-
dc.contributor.authorKang, DK-
dc.contributor.authorKim, TH-
dc.contributor.authorYim, H-
dc.contributor.authorChun, M-
dc.contributor.authorPark, MC-
dc.contributor.authorChang, SJ-
dc.date.accessioned2014-03-19T05:25:20Z-
dc.date.available2014-03-19T05:25:20Z-
dc.date.issued2012-
dc.identifier.issn1226-1769-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/9747-
dc.description.abstractAmong 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.-
dc.language.isoen-
dc.titleRisk Reducing Surgery in Carriers with Double Heterozygosity for BRCA1 and BRCA2 Mutations-
dc.typeArticle-
dc.subject.keywordBreast neoplasms-
dc.subject.keywordBRCA1 gene-
dc.subject.keywordBRCA2 gene-
dc.subject.keywordMastectomy-
dc.contributor.affiliatedAuthor홍, 우성-
dc.contributor.affiliatedAuthor김, 구상-
dc.contributor.affiliatedAuthor정, 용식-
dc.contributor.affiliatedAuthor강, 석윤-
dc.contributor.affiliatedAuthor강, 두경-
dc.contributor.affiliatedAuthor김, 태희-
dc.contributor.affiliatedAuthor임, 현이-
dc.contributor.affiliatedAuthor전, 미선-
dc.contributor.affiliatedAuthor박, 명철-
dc.contributor.affiliatedAuthor장, 석준-
dc.type.localJournal Papers-
dc.citation.titleJournal of genetic medicine-
dc.citation.title대한의학유전학회지-
dc.citation.volume9-
dc.citation.number1-
dc.citation.date2012-
dc.citation.startPage25-
dc.citation.endPage30-
dc.identifier.bibliographicCitationJournal of genetic medicine, 9(1):25-30, 2012-
dc.identifier.eissn2233-9108-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
Journal Papers > School of Medicine / Graduate School of Medicine > Radiology
Journal Papers > School of Medicine / Graduate School of Medicine > Pathology
Journal Papers > School of Medicine / Graduate School of Medicine > Radiation Oncology
Journal Papers > School of Medicine / Graduate School of Medicine > Plastic & Reconstructive Surgery
Journal Papers > School of Medicine / Graduate School of Medicine > Obstetrics & Gynecology
Journal Papers > School of Medicine / Graduate School of Medicine > Surgery
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