日本brca2阳性非侵袭性乳腺癌同时双侧乳房切除术和RRSO: 1例报告和初步经验分析

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2023-11-13 DOI:10.1186/s13053-023-00268-y
Aya Tanaka, Megumi Matsumoto, Mami Takao, Shoko Miura, Yuri Hasegawa, Ryota Otsubo, Hiroko Hayashi, Ichiro Isomoto, Kiyonori Miura, Takeshi Nagayasu
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引用次数: 0

摘要

背景:在日本,自2020年4月以来,遗传性乳腺癌和卵巢癌(HBOC)综合征的基因检测、监测和降低风险的手术已被纳入日本国民保险体系。另一方面,目前的情况是,即使是HBOC患者,医疗保健,包括对未确诊(无癌症)患者的监测,也是自费的。我们报告了一个病例,在无癌HBOC监测期间,患者自费在早期诊断出乳腺癌,并在乳腺癌治疗的同时进行了降低风险的手术。病例介绍:患者为63岁女性。她的妹妹在30多岁时有乳腺癌病史,通过基因检测发现是BRCA2致病变异携带者。因此,患者来到我院遗传科进行基因检测(自费)。在同一位点发现了一种致病变异。在患者自费的年度乳腺和卵巢监测中,一位在乳腺磁共振造影(MRI)方面有足够专业知识的医生注意到乳房MRI造影增强模式的变化,并进行了穿刺活检,发现导管原位癌。在患者的要求下,除乳腺癌治疗外,她同时接受了对侧降低风险的乳房切除术和降低风险的输卵管卵巢切除术。结论:我们遇到了一个病例,在癌症治疗和降低风险的手术同时进行致病变异携带者,他非常担心患癌症。对无癌BRCA1/2突变携带者的监测和扩大手术保险范围是未来重要的问题。
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Simultaneous bilateral mastectomy and RRSO for BRCA2-positive non-invasive breast cancer in Japan: a case report and analysis of initial experience.

Background: In Japan, genetic testing, surveillance, and risk-reducing surgery for hereditary breast and ovarian cancer (HBOC) syndrome have been covered by the Japanese national insurance system since April 2020. On the other hand, the current situation is that medical care, including surveillance of undiagnosed (cancer-free) patients, is self-funded even for individuals with HBOC. We report a case in which breast cancer was diagnosed at an early stage during surveillance for cancer-free HBOC at the patient's own expense, and risk-reducing surgery was performed at the same time as treatment for breast cancer.

Case presentation: The patient was a 63-year-old woman. Her sister had a history of breast cancer in her 30s and was found to be a BRCA2 pathogenic variant carrier by genetic testing. The patient therefore presented to the genetic department of our hospital and underwent genetic testing (out-of-pocket). A pathogenic variant was found at the same site. During annual breast and ovarian surveillance at the patient's own expense, a physician with sufficient expertise in contrast-enhanced breast magnetic resonance imaging (MRI) noticed a change in the contrast enhancement pattern on breast MRI and performed needle biopsy, revealing ductal carcinoma in situ. At the request of the patient, she underwent concurrent contralateral risk-reducing mastectomy and risk-reducing salpingo-oophorectomy in addition to breast cancer treatment.

Conclusions: We encountered a case in which cancer treatment and risk-reducing surgery were performed at the same time for a pathogenic variant carrier who was very anxious about developing cancer. Surveillance of cancer-free BRCA1/2 mutation carriers and expansion of insurance coverage for surgery are important future issues.

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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
期刊最新文献
BRCA2 germline mutation carrier with five malignancies: a case report. A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives. Breast cancer and ATM mutations: treatment implications. Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2023". Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing.
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