同步胰腺肿瘤累及胰腺导管腺癌:病例报告的系统回顾。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Daniel Paramythiotis, Eleni Karlafti, Dimitrios Tsavdaris, Alexandros Mekras, Aristeidis Ioannidis, Stavros Panidis, Elizabeth Psoma, Panos Prassopoulos, Antonios Michalopoulos
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引用次数: 0

摘要

背景:胰腺导管腺癌是最常见的胰腺恶性肿瘤,其特点是预后不良。罕见的是,患者可能同时发生PDAC和另一种不同的原发性胰腺肿瘤,如胰腺神经内分泌肿瘤。本系统综述整合了已发表的病例报告,描述了同步PDAC和其他胰腺恶性肿瘤患者的表现、影像学特征、管理和结果。方法:综合检索PubMed和Scopus,确定26例相关病例报告,纳入标准集中于组织学证实的同步胰腺肿瘤,排除转移性疾病。结果:大多数患者表现为双胰腺病变,常位于胰腺体和尾部。诊断成像方式,如计算机断层扫描和内窥镜超声,揭示了共同的发现。肿瘤标志物,特别是CA 19-9,经常升高,有助于诊断。手术方式也根据肿瘤的位置和分期而有所不同,从惠普尔手术到全胰切除术。术后常采用化疗。值得注意的是,淋巴结受累和较大的肿瘤大小与较差的预后相关。结论:总之,这些患者可能表现出常见或不常见的临床表现以及实验室和影像学表现,构成了重要而独特的诊断和治疗挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synchronous Pancreatic Neoplasms Involving Pancreatic Ductal Adenocarcinoma: A Systematic Review of Case Reports.

Background: Pancreatic ductal adenocarcinoma (PDAC) is the most common pancreatic malignancy and is characterized by a very unfavorable prognosis. Rarely, patients may develop synchronous PDAC and another distinct primary pancreatic tumor, such as a pancreatic neuroendocrine tumor. This systematic review consolidates published case reports describing the presentation, imaging characteristics, management, and outcomes of patients with synchronous PDAC and other pancreatic malignancies. Methods: A comprehensive search of PubMed and Scopus identified 26 relevant case reports, with inclusion criteria focused on histologically confirmed synchronous pancreatic tumors and exclusion of metastatic disease. Results: The majority of patients present with two pancreatic lesions, often located in both the body and tail of the pancreas. Diagnostic imaging modalities, such as computed tomography and endoscopic ultrasound, reveal common findings. Tumor markers, particularly CA 19-9, are often elevated and aid in the diagnosis. Surgical approaches also vary according to tumor location and staging, with procedures ranging from Whipple surgery to total pancreatectomy. Chemotherapy is frequently employed postoperatively. Notably, lymph node involvement and larger tumor size are associated with poorer prognoses. Conclusions: In conclusion, these patients may present with a common or non-common clinical picture as well as laboratory and imaging findings, constituting an important and unique diagnostic and therapeutic challenge.

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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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