subepithelial lesion

上皮下病变
  • 文章类型: Case Reports
    在内窥镜检查期间经常遇到肠上皮下病变。病因可以包括胃肠壁内在或外在的病变。由于简单的粘膜活检通常无法诊断,因此它们可能存在诊断困境。特征射线照相的组合,内窥镜,和内镜特征可以帮助明确的诊断,从而排除了对外部压迫病因进行不必要的组织采样的需要。Retzius空间的位置是阴茎假体泵储液器插入的传统位置,可能会导致盲肠压迫。我们介绍了一种罕见的阴茎假体泵储液器,在内窥镜检查中表现为盲肠上皮下肿块。
    Intestinal subepithelial lesions are often encountered during endoscopy. Etiologies can include lesions intrinsic or extrinsic to the gastrointestinal wall. They can present a diagnostic dilemma as simple mucosal biopsies are often nondiagnostic. The combination of characteristic radiographic, endoscopic, and endosonographic features can aid in a definitive diagnosis precluding the need for unnecessary tissue sampling of extrinsic compressive etiologies. The location of the space of Retzius which is the traditional site of penile prosthetic pump reservoir insertion can predispose to cecal compression. We present a rare case of a penile prosthetic pump reservoir presenting as a cecal subepithelial mass on endoscopy.
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  • 文章类型: Journal Article
    对于在超声内镜(EUS)成像中显示低回声肿块(HM)的胃上皮下病变(GSEL),使用常规细针抽吸针(EUS-TA-CFNAN)进行EUS引导组织采集的实用性和组织学类型的频率尚不清楚.本研究旨在探讨这一问题。
    这项前瞻性观察性研究招募了291名连续接受EUS-TA-CFNAN治疗的GSEL患者,这些患者在EUS成像中显示HM(GSELHM)。对所有EUS-TA-CFNAN和手术切除的标本进行免疫组织化学分析。主要结局指标是EUS-TA-CFNAN的技术结果和GSELHM中组织学类型的频率。
    使用常规细针抽吸针的内窥镜超声引导组织采集对GSELHM的诊断率为80.1%(95%置信区间[CI]:75.0-84.5,233/291)。胃窦(P=0.004)和小于2cm的病变(P=0.003)显着降低。无不良事件发生。EUS-TA-CFNAN的免疫组化诊断包括149例胃肠道间质瘤(GIST)(51.2%),平滑肌瘤48例(16.5%),神经鞘瘤11例(3.8%),异位胰腺8例(2.7%),上皮下病变样癌5例(1.7%),其他病变12例(4.1%),58例不可诊断的病变(19.9%)。GSELHM中恶性或潜在恶性肿瘤的发生率为55.0%(95%CI:49.1-60.8,160/291)。根据最终的EUS-TA-CFNAN结果,对149例患者进行了手术,其中EUS-TA-CFNAN的诊断准确率为97.3%(95%CI:94.7-99.9,145/149).
    将EUS-TA-CFNAN用于GSELHM是安全且准确的。表现出低回声肿块的胃上皮下病变具有相当高的恶性或潜在恶性肿瘤的可能性。包括GISTS。
    UNASSIGNED: For gastric subepithelial lesions (GSELs) showing a hypoechoic mass (HM) on endoscopic ultrasonography (EUS) imaging, the utility of EUS-guided tissue acquisition using conventional fine-needle aspiration needles (EUS-TA-CFNAN) and the frequency of histological types remain unclear. This study aimed to examine this issue.
    UNASSIGNED: This prospective observational study enrolled 291 consecutive patients who underwent EUS-TA-CFNAN for GSELs showing an HM (GSELHM) on EUS imaging. Immunohistochemical analysis was performed for all EUS-TA-CFNAN and surgically resected specimens. The main outcome measures were the technical results of EUS-TA-CFNAN and the frequency of histological types in GSELHM.
    UNASSIGNED: The endoscopic ultrasound-guided tissue acquisition using conventional fine-needle aspiration needle diagnosis rate for GSELHM was 80.1% (95% confidence interval [CI]: 75.0-84.5, 233/291). It was significantly lower for antrum (P = 0.004) and lesions smaller than 2 cm (P = 0.003). There were no adverse events. The immunohistochemical diagnoses of EUS-TA-CFNAN included 149 cases of gastrointestinal stromal tumour (GIST) (51.2%), 48 cases of leiomyoma (16.5%), 11 cases of schwannoma (3.8%), 8 cases of the ectopic pancreas (2.7%), 5 cases of subepithelial lesion like cancer (1.7%), 12 cases of other lesions (4.1%), and 58 cases of undiagnosable lesions (19.9%). The frequency of malignant or potentially malignant tumour in GSELHM was 55.0% (95% CI: 49.1-60.8, 160/291). Surgery was performed in 149 patients according to the conclusive EUS-TA-CFNAN results, in which the diagnostic accuracy of EUS-TA-CFNAN was 97.3% (95% CI: 94.7-99.9, 145/149).
    UNASSIGNED: The use of EUS-TA-CFNAN for GSELHMs is safe and accurate. Gastric subepithelial lesions showing a hypoechoic mass have a reasonably high possibility of containing malignant or potentially malignant tumours, including GISTs.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    十二指肠神经内分泌肿瘤(NETs)是罕见的上皮下肿瘤,由上皮层下的神经内分泌细胞引起。然而,如果仅使用常规内窥镜钳活检获取组织样本,则很难进行准确的组织病理学诊断。这项研究旨在评估十二指肠NETs的窄带成像放大内镜(ME-NBI)发现。我们回顾性分析了2011年1月至2022年6月期间接受ME-NBI的21例患者的22个十二指肠NETs数据库。ME-NBI,超声检查,并分析十二指肠NETs的组织病理学发现。19个病灶位于球部,两个位于十二指肠上角,一个位于十二指肠的第二部分。18个病变(82%)有IIa形态,9人(41%)表面有中央凹陷。在内窥镜超声检查中,几乎所有病变(20/22,91%)位于第二层和/或第三层,中位肿瘤大小为6毫米。在ME-NBI期间,18个病变(82%)的微表面模式是规则的,4个病变(18%)的微表面模式不存在.17个病变(77%)的微血管模式是规则的,不规则的4(18%),在1个(5%)中不存在。在15个(68%)病变中观察到上皮下血管增厚。根据是否存在增厚的上皮下血管,肿瘤大小没有差异(6.1±1.8mm与5.9±3.8mm,p=0.860)。总之,十二指肠NETs的特征性ME-NBI表现为规则的微表面和微血管模式以及存在增厚的上皮下血管.这些ME-NBI特征可用于区分十二指肠NETs与其他十二指肠上皮下病变。
    Duodenal neuroendocrine tumors (NETs) are rare subepithelial tumors that arise from the neuroendocrine cells beneath the epithelial layer. However, an accurate histopathological diagnosis is difficult when tissue samples are obtained using conventional endoscopic forceps biopsy alone. This study aimed to evaluate the magnifying endoscopy with narrow-band imaging (ME-NBI) findings of duodenal NETs. We retrospectively analyzed a database of 22 duodenal NETs from 21 patients who underwent ME-NBI between January 2011 and June 2022. The ME-NBI, endosonographic, and histopathologic findings of duodenal NETs were analyzed. Nineteen lesions were located in the bulb, two were located in the superior duodenal angle, and one was located in the second portion of the duodenum. Eighteen lesions (82%) had IIa morphology, and nine (41%) had central depression on the surface. On endoscopic ultrasonography, almost all lesions (20/22, 91%) were located in the second and/or third layers, and the median tumor size was 6 mm. During ME-NBI, the microsurface pattern was regular in 18 lesions (82%) and absent in 4 (18%). The microvascular pattern was regular in 17 lesions (77%), irregular in 4 (18%), and absent in 1 (5%). Thickened subepithelial vessels were observed in 15 (68%) lesions. There was no difference in tumor size according to the presence or absence of thickened subepithelial vessels (6.1 ± 1.8 mm vs. 5.9 ± 3.8 mm, p = 0.860). In conclusion, the characteristic ME-NBI findings of duodenal NETs were regular microsurface and microvascular patterns and the presence of thickened subepithelial vessels. These ME-NBI features may be useful for differentiating duodenal NETs from other duodenal subepithelial lesions.
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  • 文章类型: Journal Article
    背景:内窥镜超声检查(EUS)被推荐为评估胃上皮下病变(SEL)的最佳工具;尽管如此,它难以区分胃肠道间质瘤(GIST)与平滑肌瘤和神经鞘瘤。GIST具有恶性潜能,而平滑肌瘤和神经鞘瘤被认为是良性的。
    目的:本研究旨在建立基于EUS图像的联合影像组学模型,以区分胃中GIST与平滑肌瘤和神经鞘瘤。
    方法:经病理证实的GIST的EUS图像,平滑肌瘤,和神经鞘瘤从五个中心收集。基于随机分裂样本方法(7:3)将胃SELs分为训练数据集和测试数据集。从肿瘤和固有肌层区域提取放射学特征。主成分分析,最小绝对收缩率,和选择运算符用于特征选择。采用支持向量机构建影像组学模型。建立了两个影像组学模型:常规影像组学模型仅包括肿瘤特征,而联合影像组学模型结合了肿瘤和固有肌层区域的特征。
    结果:共纳入485例的3933张EUS图像。对于平滑肌瘤和神经鞘瘤的GIST的鉴别诊断,准确性,灵敏度,特异性,受试者工作特性曲线下面积为74.5%,72.2%,78.7%,和0.754,分别EUS专家;76.8%,74.4%,81.0%,和0.830,分别对于传统的放射学模型;和90.9%,91.0%,90.6%,和0.953,分别用于组合放射学模型。对于胃SELs<20mm,准确性,灵敏度,特异性,联合影像组学模型的受试者工作特征曲线下面积为91.4%,91.6%,91.1%,和0.960。
    结论:我们开发并验证了一种联合影像组学模型来区分胃GIST与平滑肌瘤和神经鞘瘤。联合影像组学模型显示出比常规影像组学模型更好的诊断性能,可以帮助EUS专家非侵入性诊断胃SELs。特别是胃SEL<20mm。
    BACKGROUND: Endoscopic ultrasonography (EUS) is recommended as the best tool for evaluating gastric subepithelial lesions (SELs); nonetheless, it has difficulty distinguishing gastrointestinal stromal tumors (GISTs) from leiomyomas and schwannomas. GISTs have malignant potential, whereas leiomyomas and schwannomas are considered benign.
    OBJECTIVE: This study aimed to establish a combined radiomic model based on EUS images for distinguishing GISTs from leiomyomas and schwannomas in the stomach.
    METHODS: EUS images of pathologically confirmed GISTs, leiomyomas, and schwannomas were collected from five centers. Gastric SELs were divided into training and testing datasets based on random split-sample method (7:3). Radiomic features were extracted from the tumor and muscularis propria regions. Principal component analysis, least absolute shrinkage, and selection operator were used for feature selection. Support vector machine was used to construct radiomic models. Two radiomic models were built: the conventional radiomic model included tumor features alone, whereas the combined radiomic model incorporated features from the tumor and muscularis propria regions.
    RESULTS: A total of 3933 EUS images from 485 cases were included. For the differential diagnosis of GISTs from leiomyomas and schwannomas, the accuracy, sensitivity, specificity, and area under the receiver operating characteristic curve were 74.5%, 72.2%, 78.7%, and 0.754, respectively, for the EUS experts; 76.8%, 74.4%, 81.0%, and 0.830, respectively, for the conventional radiomic model; and 90.9%, 91.0%, 90.6%, and 0.953, respectively, for the combined radiomic model. For gastric SELs <20 mm, the accuracy, sensitivity, specificity, and area under the receiver operating characteristic curve of the combined radiomic model were 91.4%, 91.6%, 91.1%, and 0.960, respectively.
    CONCLUSIONS: We developed and validated a combined radiomic model to distinguish gastric GISTs from leiomyomas and schwannomas. The combined radiomic model showed better diagnostic performance than the conventional radiomic model and could assist EUS experts in non-invasively diagnosing gastric SELs, particularly gastric SELs <20 mm.
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  • 文章类型: Case Reports
    炎性肌纤维母细胞瘤(IMT)是一种罕见的由肌成纤维细胞构成的炎性血细胞浸润肿瘤。它通常发生在肺部,很少发生在食道。我们在此报告了一个起源于食管的IMT的有价值的病例。一名患有吞咽困难的60岁日本女性在宫颈食管有一个大的上皮下病变(SEL),长度为15厘米。手术切除证实病理诊断并改善症状。术后诊断为IMT由多发结节构成。术后1年内无复发或转移。
    Inflammatory myofibroblastic tumor (IMT) is a rare tumor composed of myofibroblasts with inflammatory blood cell infiltration. It commonly occurs in the lungs and rarely in the esophagus. We herein report a valuable case of IMT originating in the esophagus. A 60-year-old Japanese woman with dysphagia had a large subepithelial lesion in the cervical esophagus, which was 15 cm in length. Surgical resection was performed to confirm the pathological diagnosis and improve the symptoms. The postoperative diagnosis was IMT composed of multiple nodules. There was no recurrence or metastasis within one year after surgery.
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  • 文章类型: Case Reports
    背景:粘膜下肿瘤(SMT)样胃癌是罕见的,几乎所有病例都接受了根治性手术治疗,因为粘膜下层通常被肿瘤细胞深度侵入,或者因为SMT样胃癌的组织病理学类型未分化或低分化。几年来,尚未发布有关仅通过内镜切除术治愈的SMT样胃癌或此类肿瘤的内镜特征变化的报告。
    方法:我们描述了一例例外情况:一名53岁的男性,在胃窦通过食管胃十二指肠镜检查(EGD)发现了一个1.5cm大小的SMT样病变,并覆盖了正常的粘膜。内窥镜超声(EUS)可视化均匀,由第二超声层引起的界限良好的低回声病变,并伴随着第三超声层的细微消失。最初的内镜活检为肿瘤阴性。患者拒绝接受侵入性手术,随后失去了随访。在初次发现三年后,EGD显示病变明显红斑,在初次EGD后4年,它的大小增加到1.8cm,并出现中央性溃疡和异质EUS回声。最后,进行内镜黏膜下剥离术(ESD),组织病理学检查显示,中分化腺癌轻微侵犯粘膜下层(浸润深度169μm),但无淋巴管浸润,切缘阴性。幸运的是,不需要额外的手术治疗.他在ESD后随访了4年,没有任何局部或远处复发的证据。
    结论:本报告描述了一例极为罕见的早期胃癌,表现为SMT,在治疗延迟4年后通过ESD治愈,以及在此期间发生的内镜改变。该报告强调了在临床实践中遇到SMT时考虑胃癌可能性的重要性。
    BACKGROUND: Submucosal tumor (SMT)-like gastric cancer is rare, and almost all cases undergo curative surgical treatment because the submucosal layer is usually deeply invaded by tumor cells or because histopathologic types of SMT-like gastric cancer are undifferentiated or poorly differentiated. No report has been issued on an SMT-like gastric cancer cured by endoscopic resection alone or on changes in the endoscopic features of this type of tumor over several years.
    METHODS: We describe an exceptional case of a 53-year-old male with a 1.5 cm-sized SMT-like lesion covered by normal-appearing mucosa discovered by esophagogastroduodenoscopy (EGD) at the gastric antrum. Endoscopic ultrasound (EUS) visualized a homogeneous, well-circumscribed hypoechogenic lesion arising from the second sonographic layer with associated subtle obliteration of the third sonographic layer. Initial endoscopic biopsy was negative for neoplasm. The patient refused to undergo an invasive procedure and was subsequently lost to follow-up. Three years after initial detection, EGD revealed the lesion had become markedly erythematous, and at 4 years after initial EGD it had increased in size to 1.8 cm and developed a central ulcer and a heterogeneous EUS echo. Finally, endoscopic submucosal dissection (ESD) was performed, and histopathologic examination revealed a moderately differentiated adenocarcinoma had minutely invaded the submucosal layer (invasion depth 169 μm) but without lymphovascular invasion and with negative resection margins. Fortunately, no additional surgical treatment was required. He has been followed for 4 years after ESD without any evidence of local or distant recurrence.
    CONCLUSIONS: This report describes an extremely rare case of early gastric cancer presenting as SMT that was cured by ESD after a treatment delay of 4 years and the endoscopic changes that occurred during this period. The report highlights the importance of considering the possibility of gastric cancer when SMT is encountered in clinical practice.
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  • 文章类型: Case Reports
    通常在食管胃十二指肠镜检查期间偶然发现胃上皮下病变(SEL)。大多数胃SELs是良性病变,如平滑肌瘤和胰腺休息。然而,肿瘤病变包括神经内分泌肿瘤,胃肠道间质瘤,和某些类型的胃腺癌(GA),例如最近WHO分类的胃底腺型腺癌,可以找到。缺乏简单和成熟的SEL诊断方法仍然是临床挑战。由于病变的上皮下位置,标准活检对于诊断是次优的,因此经常被忽略。此外,基于准则的诊断SEL的算法在日本和美国之间也有所不同。在这个系列中,我们描述了三例随后被诊断为GA的胃SEL病例。病例1为胃底腺型(主要细胞为主型)腺癌;病例2为低分化GA;病例3为晚期GA,在对SEL进行连续4年的内窥镜随访后发现。虽然标准活检导致前2例成功诊断,病例3在监测期间未进行标准活检,这使得其诊断有效性不明确.第三例强调了纵向观察内窥镜粘膜改变的重要性,这可能提示某些类型的GA。临床医生应该意识到标准活检可能在评估恶性胃SEL样病变中起重要作用。至关重要的是,要对SEL的表面变化保持警惕,而不是立即忽略标准活检。
    Gastric subepithelial lesions (SEL) are usually found incidentally during esophagogastroduodenoscopy. Most gastric SELs are benign lesions, such as leiomyoma and pancreatic rests. However, neoplastic lesions including neuroendocrine tumors, gastrointestinal stromal tumors, and certain types of gastric adenocarcinoma (GA), such as the recently WHO-classified fundic gland type adenocarcinoma, may be found. The lack of simple and established diagnostic methods for SEL remains a clinical challenge. Standard biopsy is suboptimal for diagnosis due to the subepithelial location of lesions and is therefore often omitted. Furthermore, guideline-based algorithmic approaches for diagnosing SEL also differ between Japan and the USA. In this case series, we describe three cases of gastric SEL that were subsequently diagnosed as GA. Case 1 was a fundic gland type (chief cell predominant type) adenocarcinoma; Case 2 was a poorly differentiated GA; Case 3 was an advanced GA, found after 4 serial years of endoscopic follow-up for SEL. While standard biopsy led to successful diagnosis in the first 2 cases, no standard biopsy was performed during surveillance in Case 3, making its diagnostic effectiveness unclear. The third case highlights the importance of longitudinal observation for endoscopic mucosal alterations that may suggest certain types of GA. Clinicians should be aware that standard biopsy may play an important role in the evaluation of malignant gastric SEL-like lesions. It is crucial to remain vigilant for surface changes in SEL and not to summarily omit standard biopsy.
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  • 文章类型: Case Reports
    粘膜相关淋巴组织(MALT)的结外边缘区淋巴瘤并不常见,并且由于临床表现和内窥镜表现伪装成其他病理而难以诊断。很少,它与急性上消化道(GI)出血有关。我们报道了一名60岁的男性,他出现了急性上消化道出血和内窥镜检查结果,提示孤立的胃静脉曲张(GV),最终确定为MALT淋巴瘤。放射治疗可以完全缓解,在12个月的随访中没有复发。该病例突出了MALT淋巴瘤的独特临床和内窥镜表现,提供者应该注意。我们强调使用内窥镜超声(EUS)评估以进行准确诊断。
    Extra-nodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT) is uncommon and difficult to diagnose due to varied clinical presentations and endoscopic appearances masquerading as other pathology. Rarely, it has been associated with acute upper gastrointestinal (GI) bleeding. We report on a 60-year-old male who presented with an acute upper GI bleed and endoscopic findings suggestive of isolated gastric varices (GV), ultimately determined to be MALT lymphoma. Complete remission was achieved with radiation therapy, with no recurrence at a 12-month follow-up. This case highlights a unique clinical and endoscopic presentation of MALT lymphoma which providers should be aware of. We emphasize the use of endoscopic ultrasound (EUS) evaluation for accurate diagnosis.
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