多种原发恶性肿瘤患者的种系BRCA2突变和Lynch综合征

IF 0.6 Q4 ONCOLOGY
Case Reports in Oncological Medicine Pub Date : 2025-08-20 eCollection Date: 2025-01-01 DOI:10.1155/crom/5879510
Morgan M Puglisi, Natasha N Dziarnowski, Bohdan Baralo, Hetal Vachhani
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引用次数: 0

摘要

简介:缺乏BRCA基因会导致DNA修复障碍,并与乳腺癌、卵巢癌、前列腺癌、胰腺癌和黑色素瘤的终生风险增加有关。Lynch综合征是由负责DNA错配修复的基因的遗传突变引起的,导致结直肠、子宫内膜、卵巢、胃、泌尿、胰腺和中枢神经系统恶性肿瘤的终生风险增加。在这里,我们提出了一个罕见的患者共存的BRCA2和PSM2突变在转移性胰腺癌和前列腺癌的设置。病例介绍:患者最初在57岁时被诊断为转移性前列腺癌,当PSA筛查为22.9时,活检和分期扫描显示主动脉腔淋巴结受累。开始用雄激素剥夺疗法加用阿比特龙和强的松。此外,PET扫描显示一个高代谢孤立的肺结节,楔形切除后显示为I期肺癌。三年后,在监视扫描中发现胰腺肿块和多个肝脏病变。活检证实了胰腺癌的诊断,种系检测显示BRCA2和PMS2突变共存。根据POLE研究,患者完成了顺铂和吉西他滨的四个周期,随后开始使用奥拉帕尼。在诊断为转移性胰腺癌后约12个月,诊断为转移性前列腺癌后约4年,患者病情控制良好,运动状态ECOG 0,维持治疗副作用最小。结论:本病例是两种遗传综合征共存的独特组合,合并发病率约为1:35 . 7 000。本例患者存在两种晚期恶性肿瘤,强调了DNA修复途径联合缺陷的累积效应,并可能导致更高的终身癌症风险。这也许可以解释肺癌的存在与最小吸烟史少于10包年。PARP抑制剂可能有效控制转移性胰腺癌,因此,遗传咨询对该患者及其家庭成员很重要,他们将需要适当的癌症筛查。由于下一代测序和种系检测,携带两种致病变异的可能性可能会增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Germline BRCA2 Mutation and Lynch Syndrome in a Patient With Multiple Primary Malignancies.

Introduction: Deficiency in BRCA genes leads to impediment in DNA repair and is associated with an increased lifetime risk of breast, ovarian, prostate, and pancreatic cancer and melanoma. Lynch syndrome is caused by inherited mutations in genes responsible for DNA mismatch repair, with resultant increase in lifetime risk of colorectal, endometrial, ovarian, stomach, urinary, pancreatic, and CNS malignancies. Here, we present a patient with a rare coexistence of both BRCA2 and PSM2 mutation in the setting of metastatic pancreatic and prostate cancer. Case Presentation: The patient was initially diagnosed with metastatic prostate adenocarcinoma at the age of 57, when a screening PSA of 22.9 warranted biopsy and staging scans revealed involvement of the aortocaval lymph node. Treatment with androgen deprivation therapy with the addition of abiraterone and prednisone was initiated. Additionally, a PET scan showed a hypermetabolic isolated lung nodule, which upon wedge resection showed Stage I lung cancer. Three years later, a pancreatic mass and multiple liver lesions were found on a surveillance scan. Biopsy confirmed the diagnosis of pancreatic cancer, and germline testing revealed the coexistence of BRCA2 and PMS2 mutations. The patient completed four cycles of cisplatin and gemcitabine, followed by the initiation of olaparib as per the POLE study. About 12 months after the diagnosis of metastatic pancreatic cancer and 4 years after the diagnosis of metastatic prostate cancer, the patient has excellent control of the disease with performance status ECOG 0 and minimal side effects from maintenance therapy. Conclusion: This case presents a unique combination of two coexistent inherited syndromes with the approximate combined incidence of 1:357,000. The presence of two advanced malignancies in our patient underlines the cumulative effects of combined deficiency in the DNA repair pathway and possibly an even higher lifetime risk of cancer. This may explain the presence of lung cancer with a minimal smoking history of less than 10 pack years. PARP inhibitors may be effective in controlling metastatic pancreatic cancer, and thus, genetic counseling is important for this patient and his family members, who will need appropriate cancer screening. The probability of carrying two pathogenic variants may be expected to increase as a result of next-generation sequencing and germline testing.

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来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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