High-grade and Invasive Intraductal Papillary Mucinous Neoplasm of the Pancreas with STK11 Aberration Having Undergone Pancreatic Resection Three Times for Metachronous Intrapancreatic Recurrences: A Case Report and Review of the Literature.

IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Internal Medicine Pub Date : 2025-11-15 Epub Date: 2025-05-15 DOI:10.2169/internalmedicine.5076-24
Hideyuki Anan, Shinsuke Koshita, Yoshihide Kanno, Takahisa Ogawa, Hiroaki Kusunose, Toshitaka Sakai, Keisuke Yonamine, Kazuaki Miyamoto, Fumisato Kozakai, Haruka Okano, Kento Hosokawa, Masaya Oikawa, Takashi Tsuchiya, Yutaka Noda, Takashi Sawai, Taito Itoh, Yuko Omori, Toru Furukawa, Kei Ito
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引用次数: 0

Abstract

A 56-year-old woman with high-grade or invasive intraductal papillary mucinous neoplasm (IPMN) underwent 3 pancreatic surgeries for initial and recurrent IPMN lesions. Immunostaining and genetic analyses of all lesions revealed a consistent mutation in KRAS and loss of serine/threonine kinase 11 (STK11), indicating the same origin of these lesions and the possibility of intraductal dissemination. Other immunostaining findings, such as mucin expression and a high Ki-67 labeling index, were consistent among all the lesions and supported their malignant potential. IPMNs with loss of STK11 may benefit from tailored follow-up of the remnant pancreas due to their high likelihood of recurrence through intraductal spread.

Abstract Image

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胰腺高级别浸润性导管内乳头状黏液瘤伴STK11畸变三次胰腺切除术同时复发1例并文献复习
一名56岁的女性,患有高级别或侵袭性导管内乳头状粘液瘤(IPMN),因其初始和复发性IPMN病变接受了3次胰腺手术。所有病变的免疫染色和遗传分析显示KRAS的一致突变和STK11的缺失,表明这些病变的起源相同,可能是导管内播散。其他免疫染色结果,如MUC表达和高Ki-67标记指数,在所有病变中都是一致的,并支持其恶性潜能。STK11缺失的IPMNs可能受益于残胰腺的定制随访,因为它们通过导管内扩散复发的可能性很高。
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来源期刊
Internal Medicine
Internal Medicine 医学-医学:内科
CiteScore
1.90
自引率
8.30%
发文量
0
审稿时长
2.2 months
期刊介绍: Internal Medicine is an open-access online only journal published monthly by the Japanese Society of Internal Medicine. Articles must be prepared in accordance with "The Uniform Requirements for Manuscripts Submitted to Biomedical Journals (see Annals of Internal Medicine 108: 258-265, 1988), must be contributed solely to the Internal Medicine, and become the property of the Japanese Society of Internal Medicine. Statements contained therein are the responsibility of the author(s). The Society reserves copyright and renewal on all published material and such material may not be reproduced in any form without the written permission of the Society.
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