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微型活检钳在腹膜癌病评估中的应用:一种可能的新适应症?

Micro-Biopsy Forceps in the Assessment of Peritoneal Carcinomatosis: A Possible New Indication?

作者信息

Binda Cecilia, Dabizzi Emanuele, Sinagra Emanuele, Fornelli Adele, Saragoni Luca, Cennamo Vincenzo, Anderloni Andrea, Fabbri Carlo

机构信息

Gastroenterology and Digestive Endoscopy Unit, Forlì - Cesena Hospitals, AUSL Romagna, Forlì-Cesena, Italy.

Gastroenterology and Interventional Endoscopy Unit, Ospedale Maggiore "C.A. Pizzardi", AUSL Bologna, Bologna, Italy.

出版信息

Clin Endosc. 2021 Jul;54(4):613-617. doi: 10.5946/ce.2020.241. Epub 2021 Mar 25.

DOI:10.5946/ce.2020.241
PMID:33765374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8357587/
Abstract

Peritoneal carcinomatosis (PC) is defined as a metastatic involvement of the peritoneum by several other primary sites and it is characterized by a marked worsening of prognosis, with limited treatment opportunities. Subsequently, PC should be ruled out before any invasive treatment is administered. A new through-the-needle micro-biopsy forceps (MF) was recently introduced that permits micro-histology cores. In this case series, we evaluated the feasibility of MF in the assessment of PC to complete patient diagnostic work-ups. Five consecutive patients referred for endoscopic ultrasound staging were sampled using MF. Sampling was feasible in all patients with a technical success of 100%. No adverse events were reported in any cases. This technique was feasible and safe with a technical success rate of 100%. It permitted sampling of peritoneal irregularity, obtained high-quality tissue fragments in all cases, and enabled an additional assessment, i.e., immunohistochemical staining.

摘要

腹膜癌病(PC)被定义为其他几个原发部位对腹膜的转移性侵犯,其特征是预后显著恶化,治疗机会有限。因此,在进行任何侵入性治疗之前,都应排除PC。最近推出了一种新型的经针微活检钳(MF),可获取微组织芯。在本病例系列中,我们评估了MF在PC评估中完成患者诊断检查的可行性。连续5例因内镜超声分期就诊的患者使用MF进行采样。所有患者的采样均可行,技术成功率为100%。所有病例均未报告不良事件。该技术可行且安全,技术成功率为100%。它允许对腹膜不规则处进行采样,在所有病例中均获得了高质量的组织碎片,并能够进行额外的评估,即免疫组化染色。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/86bcb3969014/ce-2020-241f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/e89e370805dd/ce-2020-241f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/d71c974a90a5/ce-2020-241f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/4813befe37df/ce-2020-241f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/54660e5c0379/ce-2020-241f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/86bcb3969014/ce-2020-241f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/e89e370805dd/ce-2020-241f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/d71c974a90a5/ce-2020-241f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/4813befe37df/ce-2020-241f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/54660e5c0379/ce-2020-241f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a1c/8357587/86bcb3969014/ce-2020-241f5.jpg

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