模拟原发性卵巢肿瘤的胰腺癌分离性卵巢转移:分子分析在确定诊断中的作用。

Journal of Pancreatic Cancer Pub Date : 2021-10-14 eCollection Date: 2021-01-01 DOI:10.1089/pancan.2021.0001
Catherine M Tucker, Cheryl L Godcharles, Wei Jiang, Charles J Yeo, Norman G Rosenblum, Ethan J Halpern, William E Luginbuhl, Anthony J Prestipino
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引用次数: 1

摘要

背景和表现:在这项研究中,我们报告了一位64岁的女性,主诉腹痛和腹胀,持续了4个月。影像学显示左侧胰腺6.1 cm肿块及骨盆19.1 cm多房性囊性病变,后显示其取代左侧卵巢。胰腺肿物经内镜超声引导下细针穿刺活检,细胞学检查诊断为腺癌。患者在开腹手术前接受新辅助化疗和放疗,切除胰腺和左附件肿块。对患者的治疗反应进行放射学和生化检查,检测癌抗原(CA) 19-9 (114-35 U/mL)、癌胚抗原(12-4.8 ng/mL)和CA-125 (119-15.3 U/mL)水平。随后,她接受了Appleby手术,左盆腔肿块切除术和双侧卵巢切除术。永久切片显示残余的胰腺导管癌,治疗效果良好,左卵巢多囊上皮瘤变,其区别是原发性卵巢癌与转移性疾病。结论:对卵巢肿瘤和胰腺肿瘤切片进行分子突变分析有助于诊断。在这种情况下,卵巢肿瘤显示出与治疗后的胰腺癌完全相同的突变,KRAS G12R和TP53 G245S。这提高了这些肿瘤起源于同一克隆事件的可能性。结果表明,卵巢肿瘤是胰腺原发的孤立转移,尽管两个肿瘤部位的形态学不明确。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Isolated Ovarian Metastasis from Pancreatic Cancer Mimicking Primary Ovarian Neoplasia: Role of Molecular Analysis in Determining Diagnosis.

Background and Presentation: In this study, we present the case of a 64-year-old female with a chief complaint of abdominal pain and bloating, which had been persistent over a period of 4 months. Imaging revealed a 6.1-cm left-sided pancreatic mass as well as a 19.1-cm multiloculated cystic lesion in the pelvis, later revealed to be replacing the left ovary. The pancreatic mass was biopsied through endoscopic ultrasound-guided fine needle aspiration, and diagnosed as adenocarcinoma by cytology. The patient was treated with neoadjuvant chemotherapy and radiation before laparotomy for resection of the pancreas and left adnexal mass. Her response to treatment was followed radiologically and biochemically with cancer antigen (CA) 19-9 (114-35 U/mL), carcinoembryonic antigen (12-4.8 ng/mL), and CA-125 (119-15.3 U/mL) levels. She subsequently underwent an Appleby procedure, and resection of left pelvic mass and bilateral oophorectomy. Permanent sections revealed residual pancreatic ductal carcinoma with treatment effect, and a multicystic epithelial neoplasia of the left ovary for which the differential was primary ovarian carcinoma versus metastatic disease. Conclusions: Molecular mutational analysis was performed on sections of both the ovarian tumor and the pancreatic tumor to aid in diagnosis. The ovarian tumor in this case showed exactly the same mutations, KRAS G12R and TP53 G245S, as in the treated pancreatic cancer. This raised the high probability that these tumors originated from the same clonal event. The findings suggested that the ovarian tumor was an isolated metastasis of the pancreatic primary, despite the morphologic ambiguity between the two sites of neoplasia.

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