Tissue diagnosis

组织诊断
  • 文章类型: Journal Article
    背景与研究目的淋巴结(LN)受累是肝内胆管癌(iCCA)患者的不良预后因素。这项研究的目的是评估潜在可切除iCCA患者的LN组织采集内窥镜超声检查(EUS-TA)的产量和对临床决策的影响。患者和方法在这项多中心队列研究中,我们回顾性纳入了2010~2020年可能切除iCCA和术前EUS的患者.EUS-TA的影响被定义为由于用EUS-TA发现的病理证实的阳性LN而未进行手术探查的患者的百分比。结果56例患者行EUS,91%的患者在影像学上瞄准可疑LN。LN的EUS-TA在19例患者(34%)中确认了21例LN的恶性肿瘤。在17名患者(30%)中,由于淋巴结受累,手术探查被取消。最后,24例患者(43%)接受了手术探查,其中6例患者(25%)发现了阳性区域LN。结论在横断面成像上可能切除的iCCA和可疑LN的患者中,EUS-TA在30%的患者中证实LN受累。手术探查被拒绝主要是因为手术风险高的患者的区域外LN受累和区域LN受累。
    Background and study aims Lymph node (LN) involvement is a poor prognostic factor for patients with intrahepatic cholangiocarcinoma (iCCA). The aim of this study was to evaluate the yield and impact on clinical decision making of endoscopic ultrasound with tissue acquisition (EUS-TA) of LNs in patients with potentially resectable iCCA. Patients and methods In this multicenter cohort study, patients with potentially resectable iCCA and preoperative EUS between 2010 and 2020 were retrospectively included. The impact of EUS-TA was defined as the percentage of patients who did not undergo surgical exploration due to pathologically confirmed positive LNs found with EUS-TA. Results A total of 56 patients underwent EUS, with 91% of patients to target suspicious LNs on imaging. EUS-TA of LNs confirmed malignancy in 21 LNs among 19 patients (34%). In 17 patients (30%), surgical exploration was withheld due to nodal involvement. Finally, 24 patients (43%) underwent surgical exploration among whom positive regional LNs were identified in six patients (25%). Conclusions In patients with potentially resectable iCCA and suspicious LNs on cross-sectional imaging, EUS-TA confirmed LN involvement in 30% of patients. Surgical exploration was withheld mostly because of extraregional LN involvement and regional LN involvement in patients with high surgical risk.
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  • 文章类型: Journal Article
    背景和研究目的准确的内镜下对大肠病变的表征对于预测组织学至关重要,但即使对于专家来说也很困难。简单的标准可以帮助内窥镜医师检测和预测恶性肿瘤。这项研究的目的是评估绿色标志和鸡皮肤方面在检测恶性结直肠肿瘤中的价值。患者和方法我们前瞻性地表征并评估了在筛查或转诊进行内镜切除(Pro-CONECCT研究)期间检测到的所有连续结直肠病变的组织学。我们评估了绿色标志和鸡皮肤方面的诊断准确性,以检测浅层和深层侵入性病变。结果共纳入461例患者,结直肠病变803例。对于浅层和深层浸润性病变,绿色标志的阴性预测值为89.6%(95%置信区间[CI]87.1%-91.8%)和98.1%(95%CI96.7%-99.0%)。分别。与鸡皮相比,与CONECCT分类和鸡皮相比,绿色标志显示了两种病变类型的检测的附加价值(浅表病变的校正比值比[OR]5.9;95%CI3.4-10.2;P<0.001),深部病变的校正OR为9.0;95%CI3.9-21.1;P<0.001)。结论绿色标志可能与结直肠恶性肿瘤有关。在精确分析病变之前靶向这些区域可能是改善局灶性恶性肿瘤的检测和最严重组织学预测的一种方法。
    Background and study aims Accurate endoscopic characterization of colorectal lesions is essential for predicting histology but is difficult even for experts. Simple criteria could help endoscopists to detect and predict malignancy. The aim of this study was to evaluate the value of the green sign and chicken skin aspects in detection of malignant colorectal neoplasia. Patients and methods We prospectively characterized and evaluated the histology of all consecutive colorectal lesions detected during screening or referred for endoscopic resection (Pro-CONECCT study). We evaluated the diagnostic accuracy of the green sign and chicken skin aspects for detection of superficial and deep invasive lesions. Results 461 patients with 803 colorectal lesions were included. The green sign had a negative predictive value of 89.6% (95% confidence interval [CI] 87.1%-91.8%) and 98.1% (95% CI 96.7%-99.0%) for superficial and deep invasive lesions, respectively. In contrast to chicken skin, the green sign showed additional value for detection of both lesion types compared with the CONECCT classification and chicken skin (adjusted odds ratio [OR] for superficial lesions 5.9; 95% CI 3.4-10.2; P <0.001), adjusted OR for deep lesions 9.0; 95% CI 3.9-21.1; P <0.001). Conclusions The green sign may be associated with malignant colorectal neoplasia. Targeting these areas before precise analysis of the lesion could be a way of improving detection of focal malignancies and prediction of the most severe histology.
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  • 文章类型: Journal Article
    背景和研究目的上消化道上皮下病变(SEL)的组织学确认仍然具有挑战性。SELs的内窥镜切除术因其出色的诊断率和消除持续监测的机会而越来越多地使用。在这项研究中,我们的目的是评估适应症,不同内镜下切除技术对SEL的成功率和并发症,鹿特丹三级转诊医院,荷兰。方法回顾性收集2013年10月至2021年12月的患者资料并进行分析。主要结果是R0切除率,整体切除率,复发率,和与程序相关的不良事件(AE)(Clavien-Dindo)。次要结果是手术时间,需要手术干预,以及对患者管理的临床影响。结果58例患者均接受内镜下上消化道SELs切除术。病变的中位直径为20mm(范围7-100mm)。中位随访时间为5个月(0.4-75.7)。48例(83%)成功完成,导致85%的整体切除和63%的R0切除。手术相关的AE发生在6例患者中(13%)。在三名患者中发现了严重的并发症(CD3a级)。(恶性前)诊断的局部复发率为2%。7例患者(15%)需要额外的手术干预。共有32例患者(67%)在内镜下切除后可以出院。结论内镜下切除术是一种安全有效的治疗SEL的方法,并提供了有关未确定SEL的有价值的信息,而反复取样的尝试未能提供足够的组织进行诊断。
    Background and study aims Histological confirmation of subepithelial lesions (SELs) in the upper gastrointestinal tract remains challenging. Endoscopic resection of SELs is increasingly used for its excellent diagnostic yield and opportunity to do away with continued surveillance. In this study, we aimed to evaluate the indications, success rates and complications of different endoscopic resection techniques for SELs at a large, tertiary referral hospital in Rotterdam, The Netherlands. Patients and methods Data between October 2013 and December 2021 were retrospectively collected and analyzed. Main outcomes were R0-resection rate, en bloc resection rate, recurrence rate, and procedure-related adverse events (AEs) (Clavien-Dindo). Secondary outcomes were procedure time, need for surgical intervention, and clinical impact on patient management. Results A total of 58 patients were referred for endoscopic resection of upper gastrointestinal SELs. The median diameter of lesions was 20 mm (range 7-100 mm). Median follow-up time was 5 months (range 0.4-75.7). Forty-eight procedures (83%) were completed successfully leading to en bloc resection in 85% and R0-resection in 63%. Procedure-related AEs occurred in six patients (13%). Severe complications (CD grade 3a) were seen in three patients. The local recurrence rate for (pre)malignant diagnosis was 2%. Additional surgical intervention was needed in seven patients (15%). A total of 32 patients (67%) could be discharged from further surveillance after endoscopic resection. Conclusions Endoscopic resection is a safe and effective treatment for SELs and offers valuable information about undetermined SELs for which repeated sampling attempts have failed to provide adequate tissue for diagnosis.
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  • 文章类型: Journal Article
    使用放大内窥镜对上皮下微血管内的红细胞流动进行实时可视化。然而,结肠直肠的微血管血流速度尚未研究。这里,我们旨在评估结肠息肉微血管的血流速度,并将其与周围粘膜的血流速度进行比较。我们检查了50个病灶,包括30个腺瘤(AD)和20个增生性息肉(HP)。在内窥镜切除之前,使用放大的蓝色激光成像(BLI)评估病变及其周围粘膜的血流速度。平均血流速度的计算基于使用放大BLI的分割视频图像的一个标记的红细胞的平均移动距离。AD的平均微血管血流速度(1.65±0.66mm/sec;范围0.46-2.90)明显低于HP(2.83±1.10mm/sec;1.07-4.50)或周围粘膜(3.73±1.11mm/sec;1.80-6.20;P<0.001)。与周围粘膜相比,AD的血流速度(0.41±0.16;0.10-0.82)明显低于HP的血流速度(0.89±0.25;0.46-1.51;P<0.001)。我们发现AD的平均微血管血流速度明显低于HP和周围的非肿瘤粘膜。这些发现表明,使用放大内窥镜检查具有微血管血流速度的新颖动态方法可能有助于评估AD和HP之间的生理差异。
    Real-time visualization of red blood cell flow inside subepithelial microvessels is performed with magnifying endoscopy. However, microvascular blood flow velocity in the colorectum has not been investigated. Here, we aimed to evaluate the blood flow velocity of microvessels of colonic polyps and to compare it with that of surrounding mucosa. We examined 50 lesions, including 30 adenomas (ADs) and 20 hyperplastic polyps (HPs). Blood flow velocities of lesions and their surrounding mucosa were evaluated using magnifying blue laser imaging (BLI) prior to endoscopic resection. Calculation of mean blood flow velocities was based on mean movement distance of one tagged red blood cell using split video images of magnifying BLI. Mean microvascular blood flow velocity was significantly lower in ADs (1.65±0.66 mm/sec; range 0.46-2.90) than in HPs (2.83±1.10 mm/sec; 1.07-4.50) or the surrounding mucosa (3.73±1.11 mm/sec; 1.80-6.20; P <0.001). The blood flow velocity rate compared with the surrounding mucosa was significantly lower in ADs (0.41±0.16; 0.10-0.82) than in HPs (0.89±0.25; 0.46-1.51; P <0.001). We found that mean microvascular blood flow velocity was significantly lower in ADs than in HPs and the surrounding non-neoplastic mucosa. These findings indicate that a novel dynamic approach with microvascular blood flow velocity using magnifying endoscopy may be useful in assessing physiological differences between ADs and HPs.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    背景和研究目的数字单操作员胆道镜检查(DSOC)可以诊断胆管疾病和治疗复杂的结石。然而,这些技术有局限性,如探头和工作通道的大小,成本过高,图像分辨率低。最近,一种新颖的DSOC系统(eyeMAX,Micro-Tech,南京,中国)的发展是为了解决这些限制。我们旨在基于视觉检查评估新型9F和11FDSOC系统在肿瘤诊断准确性方面的有用性和安全性。评估肿瘤扩展和实现胆管结石完全清除的能力,和与程序相关的不良事件(AE)。患者和方法对2021年7月至2022年4月接受DSOC的≥18岁患者的数据进行回顾性恢复,并分为诊断和治疗队列。结果共纳入80例患者。在诊断队列中(n=49/80),49例患者中有26例(46.9%)发现新生血管.在65.3%的患者中进行了活检,在96.8%的病例中获得了足够的组织样本。32例中有23例活检证实为肿瘤。DSOC视觉印象在诊断肿瘤方面达到91.6%的敏感性和87.5%的特异性。在治疗队列中(n=43/80),43例患者中有26例需要单独碎石术。在第一届会议中,71%的患者实现了全部结石清除。在诊断或治疗队列中均未记录早期或晚期AE。结论新型DSOC装置在区分胆道肿瘤病变方面具有出色的诊断准确性,并且在完全取石的情况下具有治疗益处。没有记录的AE。
    Background and study aims Digital single-operator cholangioscopy (DSOC) allows the diagnosis of biliary duct disorders and treatment for complicated stones. However, these technologies have limitations such as the size of the probe and working channel, excessive cost, and low image resolution. Recently, a novel DSOC system (eyeMAX, Micro-Tech, Nanjing, China) was developed to address these limitations. We aimed to evaluate the usefulness and safety of a novel 9F and 11F DSOC system in terms of neoplastic diagnostic accuracy based on visual examination, ability to evaluate tumor extension and to achieve complete biliary stone clearance, and procedure-related adverse events (AEs). Patients and methods Data from ≥ 18-year-old patients who underwent DSOC from July 2021 to April 2022 were retrospectively recovered and divided into a diagnostic and a therapeutic cohort. Results A total of 80 patients were included. In the diagnostic cohort (n = 49/80), neovascularity was identified in 26 of 49 patients (46.9%). Biopsy was performed in 65.3% patients with adequate tissue sample obtained in 96.8% of cases. Biopsy confirmed neoplasia in 23 of 32 cases. DSOC visual impression achieved 91.6% sensitivity and 87.5% specificity in diagnosing neoplasms. In the therapeutic cohort (n = 43/80), 26 of 43 patients required lithotripsy alone. Total stone removal was achieved in 71% patients in the first session. Neither early nor late AEs were documented in either the diagnostic or therapeutic cohort. Conclusions The novel DSOC device has excellent diagnostic accuracy in distinguishing neoplastic biliary lesions as well as therapeutic benefits in the context of total stone removal, with no documented AEs.
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  • 文章类型: Journal Article
    背景与研究目的胰腺癌的预后仍然很差。分子诊断和定制疗法在临床常规中变得越来越重要。患者来源,预测模型系统如类器官具有通过功能和分子表征显著增加来自活检材料的信息深度的潜力。我们比较了细针抽吸针(FNA,22G)或细针活检针(FNB,22G)影响胰腺癌患者来源的类器官(PDO)的产生,以建立类器官技术的内窥镜标准。患者和方法前瞻性评估了EUS-FNA和EUS-FNB对高度怀疑腺癌的胰腺肿块的内镜超声(EUS)引导穿刺(通过计算机断层扫描和/或磁共振成像检测)。连续患者以随机顺序接受EUS-FNA和EUS-FNB,而无需在两次通过之间更换针杆(仅更换内针类型(FNA/-B))。每种针头类型,分别获得用于组织学分析和PDO的标本.结果50例患者纳入研究。组织学显示50例中有42例(84%)为恶性肿瘤。总共从17名患者(34%)产生PDO。其中,9个仅由FNB建立,只有FNA两个,FNA和FNB都有6个。组织学显示17例PDO病例中有13例(76%)为恶性肿瘤。在两个组织学假阴性病例中,可以建立PDO。结论EUS-FNB在成功生成PDO方面优于EUS-FNA,尽管它没有显示出统计学意义。
    Background and study aims The prognosis for pancreatic cancer remains poor. Molecular diagnostics and customized therapies are becoming increasingly important in clinical routine. Patient-derived, predictive model systems such as organoids have the potential to substantially increase the depth of information from biopsy material by functional and molecular characterization. We compared the extent to which the use of fine-needle aspiration needles (FNA, 22G) or fine-needle biopsy needles (FNB, 22G) influences the generation of pancreatic cancer patient-derived organoids (PDOs) to establish endoscopic standards of organoid technology. Patients and methods Endoscopic ultrasound (EUS)-guided punctures by EUS-FNA and EUS-FNB of pancreatic masses highly suspicious for adenocarcinoma (detected by computed tomography and/or magnetic resonance imaging) were prospectively evaluated. Consecutive patients received EUS-FNA and EUS-FNB in a randomized order without the need to exchange the needle shaft (only the inner needle type (FNA/-B) was exchanged) between the passes. With each needle type, the specimens for histological analysis and for PDOs were obtained separately. Results Fifty patients were enrolled in the study. Histology revealed malignancy in 42 of 50 cases (84%). In total PDOs were generated from 17 patients (34%). Of these, nine were established by FNB only, two by FNA only, and six by both FNA and FNB. Histology revealed malignancy in 13 of 17 PDO cases (76%). In two histologically false-negative cases, PDOs could be established. Conclusions EUS-FNB was superior to EUS-FNA in terms of successful generation of PDOs, although it failed to show statistical significance.
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  • 文章类型: Editorial
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  • 文章类型: Journal Article
    背景和研究目的除了增加充分性,超声内镜(EUS)或内镜逆行胰胆管造影术(ERCP)期间的快速现场评估(ROSE)可能会影响后续治疗程序的选择和时机,但尚未探索。患者和方法这是对第三级前瞻性维护的数据库的回顾性评估,学术中心,提供ROSE和混合EUS-ERCP套件。纳入了2020年1月至2022年9月期间所有因病理证实疑似恶性肿瘤和黄疸或胃出口梗阻(GOO)的连续患者。结果541例基础恶性肿瘤患者中,323(59.7%)需要同一疗程病理诊断(男性:54.8%;年龄70[四分位距63-78];胰腺癌:76.8%,胆道腺癌16.1%)。ROSE充足率为96.6%,EUS比ERCP更高。在302例黄疸患者中,ERCP引导下支架置入术的成功率为83.1%,但由于43例EUS引导的胆道引流手术,最终引流完成了97.4%.21例GOO患者接受了15例EUS胃肠造口术和6例十二指肠支架治疗。所有58例治疗性EUS手术均在充分ROSE后进行。在ERCP引导下放置支架时,在ROSE不足(10/11;90.9%)的患者中,使用塑料支架的比例明显高于采样充足(14/240;5.8%),P<0.0001;OR161;95CI19-1352).诊断和缓解的中位住院时间为3天(范围,2-7)和中位化疗时间为33天(范围,24-47).结论近三分之二的内镜姑息治疗肿瘤患者需要现代病理诊断。ROSE充足性允许,由于索引过程,最先进的疗法标准地限于病理证实的恶性肿瘤(例如未发现的SEMS或治疗性EUS),可能减少住院时间和肿瘤治疗。
    Background and study aims Besides increasing adequacy, rapid on-site evaluation (ROSE) during endoscopic ultrasound (EUS) or endoscopic retrograde cholangiopancreatography (ERCP) may impact choices and timing of subsequent therapeutic procedures, yet has been unexplored. Patients and methods This was a retrospective evaluation of a prospectively maintained database of a tertiary, academic centre with availability of ROSE and hybrid EUS-ERCP suites. All consecutive patients referred for pathological confirmation of suspected malignancy and jaundice or gastric outlet obstruction (GOO) between Jan-2020 and Sep-2022 were included. Results Of 541 patients with underlying malignancy, 323 (59.7%) required same-session pathological diagnosis (male: 54.8%; age 70 [interquartile range 63-78]; pancreatic cancer: 76.8%, biliary tract adenocarcinoma 16.1%). ROSE adequacy was 96.6%, higher for EUS versus ERCP. Among 302 patients with jaundice, ERCP-guided stenting was successful in 83.1%, but final drainage was completed in 97.4% thanks to 43 EUS-guided biliary drainage procedures. Twenty-one patients with GOO were treated with 15 EUS-gastroenterostomies and six duodenal stents. All 58 therapeutic EUS procedures occurred after adequate ROSE. With ERCP-guided placement of stents, the use of plastic stents was significantly higher among patients with inadequate ROSE (10/11; 90.9%) versus adequate sampling (14/240; 5.8%) P <0.0001; OR 161; 95%CI 19-1352). Median hospital stay for diagnosis and palliation was 3 days (range, 2-7) and median time to chemotherapy was 33 days (range, 24-47). Conclusions Nearly two-thirds of oncological candidates for endoscopic palliation require contemporary pathological diagnosis. ROSE adequacy allows, since the index procedure, state-of-the-art therapeutics standardly restricted to pathologically confirmed malignancies (e.g. uncovered SEMS or therapeutic EUS), potentially reducing hospitalization and time to oncological treatments.
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  • 文章类型: Journal Article
    背景和研究目的关于胰腺囊性病变(PCL)患者的内镜引导组织采集(EUS-TA)的有用性的数据很少。本研究旨在确定EUS-TA与ProCore20G(PC20)的准确性,以区分粘液性瘤(MN)和非MNs(n-MN)和识别恶性PCLs。以及未通过影像学检查进行分类诊断的PCL患者的不良事件(AE)。患者和方法在这个观察中,回顾性,单中心研究,我们从2017年6月至2021年12月连续招募了所有因影像学研究诊断怀疑而接受EUS-TA的PCL患者.结果是确定EUS-TA与PC20的诊断准确性,以区分MN和n-MN,识别恶性PCLs,和AE。此处的结果,145名患者接受了EUS-TA,83名女性(57.2%),平均年龄62.2岁。平均尺寸为2.3厘米,81例患者(77.9%)PCL<3.0cm。最终诊断为EUS-TA(n=81),手术(n=58),和随访(n=6)。敏感性,特异性,阳性和阴性预测值,区分MNs和n-MNs以及识别恶性PCLs的准确率为92.6%,98.4%,98.7%,91.3%,和95.2%(κ=0.9),92%,99.2%,95.8%,98.3%,和97.9%(κ=0.93),分别。AE率为2.7%,在这个队列中没有死亡。结论EUS-TA联合PC20诊断PCL具有较高的准确性和技术成功率,且AE率低。
    Background and study aims There are rare data on the usefulness of endosonography-guided tissue acquisition (EUS-TA) in patients with pancreatic cystic lesions (PCLs). This study aimed to determine the accuracy of EUS-TA with ProCore 20G (PC20) for differentiating between mucinous neoplasia (MN) and non-MNs (n-MN) and identifying malignant PCLs, as well as its adverse events (AEs) in patients with PCLs without a classificatory diagnosis by imaging exams. Patients and methods In this observational, retrospective, single-center study, all patients with PCL who underwent EUS-TA due to diagnostic doubts in imaging studies were consecutively recruited from June 2017 to December 2021. The outcomes were to determine the diagnostic accuracy of EUS-TA with PC20 for differentiating between MN and n-MN, identifying malignant PCLs, and the AEs. Results Herein, 145 patients underwent EUS-TA, with 83 women (57.2%) and a mean age of 62.2 years. The mean size was 2.3 cm, with 81 patients (77.9%) having a PCL < 3.0 cm. The final diagnosis was made by EUS-TA (n = 81), surgery (n = 58), and follow-up (n = 6). The sensitivity, specificity, positive and negative predictive values, and accuracy for differentiating between MNs and n-MNs and identifying malignant PCLs were 92.6%, 98.4%, 98.7%, 91.3%, and 95.2% (kappa=0.9), and 92%, 99.2%, 95.8%, 98.3%, and 97.9% (kappa = 0.93), respectively. The AE rate was 2.7%, with no deaths in this cohort. Conclusions EUS-TA with PC20 has high accuracy and technical success with a low AE rate for PCL diagnosis.
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