局部晚期胰腺神经内分泌癌成功转化手术1例报告。

IF 0.7 Q4 SURGERY
Surgical Case Reports Pub Date : 2025-01-01 Epub Date: 2025-03-20 DOI:10.70352/scrj.cr.24-0064
Yuuko Tohmatsu, Mihoko Yamada, Nobuyuki Ohike, Tomoko Norose, Hidemasa Kubo, Ryo Ashida, Katsuhisa Ohgi, Shimpei Otsuka, Yoshiyasu Kato, Hideyuki Dei, Katsuhiko Uesaka, Takashi Sugino, Teiichi Sugiura
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引用次数: 0

摘要

胰腺神经内分泌癌(panNEC)是一种低分化、高度恶性的肿瘤,预后极差。这种肿瘤在最初诊断时通常表现为局部晚期或不可切除。病例介绍:一名体重减轻的72岁女性来我院就诊。计算机断层扫描显示胰腺头区一个32毫米的增强肿瘤,与肝总动脉接触超过180°。超声内镜引导下细针穿刺标本病理结果确定小细胞型NEC伴广泛坏死,诊断为局部晚期不可切除的panNEC。因此,她开始了一个疗程的卡铂和依托泊苷治疗。经过7个疗程后,鉴于肿瘤明显缩小,我们进行了胰十二指肠切除术作为转换手术。病理检查显示局部残留的NEC结节,主要由大的肿瘤细胞组成,结节内和周围散在原位癌成分。此外,生长抑素受体2在NEC各组中有弥漫膜表达。每种成分显示相同类型的KRAS突变(p.G12V),并被认为起源于胰腺的单一原发肿瘤。她接受了3个疗程的辅助化疗,24个月没有复发。结论:这是一个罕见的局部晚期,不可切除的panNEC化疗后成功转化手术的病例,提供了一些重要的组织病理学和分子见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Conversion Surgery for Locally Advanced Pancreatic Neuroendocrine Carcinoma: A Case Report.

Introduction: Pancreatic neuroendocrine carcinoma (panNEC) is a poorly differentiated, highly malignant neoplasm with an extremely poor prognosis. This tumor often presents as locally advanced or unresectable at the initial diagnosis.

Case presentation: A 72-year-old woman presented to our hospital with weight loss. A computed tomography scan showed an enhanced tumor measuring 32 mm in the pancreatic head region, with contact to the common hepatic artery over 180°. The pathological findings from the specimens obtained via endoscopic ultrasonography-guided fine-needle aspiration identified small cell-type NEC with extensive necrosis, leading to a diagnosis of locally advanced unresectable panNEC. Accordingly, she began a course of carboplatin and etoposide therapy. After 7 courses, given the significant shrinkage of the tumor, we performed a pancreatoduodenectomy as a conversion surgery. Pathological examination revealed a localized, residual nodule of NEC, consisting mainly of large neoplastic cells, with carcinoma in situ components scattered within and around the nodule. In addition, the diffuse membrane expression of somatostatin receptor 2 was observed in NEC components. Each component showed the same type of KRAS mutation (p.G12V) and was considered to originate from a single primary tumor in the pancreas. She received 3 courses of the same regimen as adjuvant chemotherapy and has remained recurrence-free for 24 months.

Conclusion: This is a rare case of successful conversion surgery for locally advanced, unresectable panNEC after chemotherapy, providing several important histopathological and molecular insights.

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