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胃肠道间质瘤手术后新发腹部肿块:难以与间叶性肿瘤鉴别的韧带样型纤维瘤病——1例报告

New Abdominal Mass After Surgery for Gastrointestinal Stromal Tumor: Desmoid-Type Fibromatosis Difficult to Distinguish from Mesenchymal Tumor - A Case Report.

作者信息

Wang Xiaodong, Shou Chunhui, Zhu Kankai, Yang Weili, Yu Jiren

机构信息

Gastroenterology Department, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, People's Republic of China.

出版信息

Int Med Case Rep J. 2024 Nov 14;17:965-969. doi: 10.2147/IMCRJ.S488459. eCollection 2024.

DOI:10.2147/IMCRJ.S488459
PMID:39559297
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11572469/
Abstract

A new lump in patients with a history of gastrointestinal stromal tumor (GIST) may indicate resistance to medication and recurrence. It is important to monitor for recurrence or metastasis after surgery for GIST, especially in cases of high-risk GIST, as it determines the subsequent treatment. However, it is difficult to differentiate between GIST and DF by imaging. Tissue biopsy and final diagnosis through pathological analysis are usually required. Here, we report 2 cases of primary diagnosis with high-risk GIST and suspected tumor recurrence during Imatinib treatment. The mass was not located where the previous GIST lesion had been. After the complete excision of the mass through laparoscopic surgery, the pathological findings revealed that it was not a recurrence of GIST, but a desmoid-type fibromatosis.

摘要

有胃肠道间质瘤(GIST)病史的患者出现新肿块可能提示对药物耐药及复发。对GIST患者术后进行复发或转移监测很重要,尤其是高危GIST患者,因为这决定后续治疗。然而,通过影像学很难区分GIST和硬纤维瘤病(DF)。通常需要进行组织活检并通过病理分析进行最终诊断。在此,我们报告2例原发性高危GIST诊断病例及伊马替尼治疗期间疑似肿瘤复发的情况。肿块并非位于先前GIST病变所在位置。通过腹腔镜手术完整切除肿块后,病理结果显示其并非GIST复发,而是韧带样型纤维瘤病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9210/11572469/b0a98a860e65/IMCRJ-17-965-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9210/11572469/64279ce0450b/IMCRJ-17-965-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9210/11572469/b0a98a860e65/IMCRJ-17-965-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9210/11572469/64279ce0450b/IMCRJ-17-965-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9210/11572469/b0a98a860e65/IMCRJ-17-965-g0002.jpg

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本文引用的文献

1
Co-targeting of ACK1 and KIT triggers additive anti-proliferative and -migration effects in imatinib-resistant gastrointestinal stromal tumors.双重靶向 ACK1 和 KIT 可在伊马替尼耐药胃肠间质瘤中产生相加的抗增殖和抗迁移作用。
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Combination of pimitespib (TAS-116) with sunitinib is an effective therapy for imatinib-resistant gastrointestinal stromal tumors.匹米替尼(TAS-116)与舒尼替尼联合使用是治疗伊马替尼耐药胃肠道间质瘤的有效疗法。
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Gastric Desmoid Fibromatosis - Report of a Rare Mimic of Gastrointestinal Stromal Tumor.
胃韧带样纤维瘤病——罕见的胃肠道间质瘤模仿病例报告
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Gastrointestinal stromal tumours.胃肠道间质瘤。
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Intra-abdominal small intestinal desmoid tumour mimicking GIST.酷似胃肠道间质瘤的腹腔内小肠硬纤维瘤
BMJ Case Rep. 2021 Feb 22;14(2):e237032. doi: 10.1136/bcr-2020-237032.
7
The management of metastatic GIST: current standard and investigational therapeutics.转移性 GIST 的治疗管理:当前标准和研究治疗方法。
J Hematol Oncol. 2021 Jan 5;14(1):2. doi: 10.1186/s13045-020-01026-6.
8
Desmoid-type fibromatosis difficult to distinguish from GIST : A case report.硬纤维瘤样纤维瘤病与 GIST 难以区分:病例报告。
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9
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