Michael G Noujaim, Claire Dorsey, Alice Parish, Daniel Raines, Lara Boudreaux, Mark Hanscom, David Cave, Donna Niedzwiecki, Daniel Wild
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This large multi-center study aims to understand the various clinical presentations, histologies and management options for SBMLs.</p><p><strong>Methods: </strong>After obtaining Institutional Review Board (IRB) approval, electronic records were used to identify all device-assisted enteroscopy (DAE) performed for luminal small bowel evaluation in adult patients at three US referral centers (Duke, LSU and UMass) from January 1, 2014, to October 1, 2020. We identified all patients within this cohort in whom a SBML was detected. Using a focused electronic medical record chart review, we collected patient, procedure, and lesion-related data and used descriptive statistics to explore relationships between these data and outcomes.</p><p><strong>Results: </strong>A total of 218 patients (49 at Duke, 148 at LSU, and 21 at UMass) in this cohort had at least one SBML found on DAE. The most common presenting symptoms were iron-deficiency anemia/bleeding (73.3%) and abnormal imaging (33.6%). Thirty-five percent of patients had symptoms for more than a year prior to their diagnosis. Most patients (71.6%) underwent video capsule endoscopy (VCE) prior to DAE and 84% of these exams showed the lesion. The lesion was seen less frequently (48.9%) on computed tomography (CT) scan performed prior to DAE. The majority of lesions were found on antegrade (56%) or retrograde (29.8%) double-balloon enteroscopy (DBE). The most common lesion phenotypes were submucosal (41.3%) and pedunculated (33%) with a much smaller number being sessile (14.7%) or obstructing/invasive (11%). They were found equally as commonly in the jejunum (46.3%) and ileum (49.5%). Most lesions were 10 - 20 mm in size (47%) but 22.1% were larger than 20 mm. The most common histologies were neuroendocrine tumors (NETs, 20.6%) and hamartomas (20.6%). Primary adenocarcinoma of the small bowel was rare, constituting only 5% of lesions. The majority of polyps (78.4%) were sporadic, compared to 21.7% associated with a polyposis or hereditary cancer syndrome, most commonly Peutz-Jeghers syndrome (18.3%). After DAE, 37.6% were advised to undergo surgical resection and 48% were advised to undergo endoscopic surveillance or no further management because of benign histology or successful endoscopic resection.</p><p><strong>Conclusions: </strong>In this multi-center retrospective study we found that SBMLs are more likely to be sporadic than syndromic, medium in size and either pedunculated or submucosal. NETs and hamartomas predominated and symptoms, most commonly anemia, can be present for more than a year prior to diagnosis. 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引用次数: 1
摘要
背景:小肠肿块性病变(Small bowel mass lesion, sbml)是一种罕见的疾病,具有多种不同的组织学和表型,我们对其认识有限。一些病变发生在公认的息肉综合征患者身上,而另一些则是零星出现的。目前的文献中,关于sbml的研究仅限于小型回顾性研究、病例报告和小型病例系列。这项大型多中心研究的目的是了解不同的临床表现,组织学和治疗方案的smml。方法:在获得机构审查委员会(IRB)批准后,电子记录用于识别2014年1月1日至2020年10月1日期间在美国三个转诊中心(Duke, LSU和UMass)对成年患者进行的腔内小肠评估的所有器械辅助肠镜检查(DAE)。我们确定了该队列中检测到SBML的所有患者。通过重点电子病历表回顾,我们收集了患者、手术和病变相关数据,并使用描述性统计来探索这些数据与结果之间的关系。结果:该队列中共有218例患者(杜克大学49例,路易斯安那州立大学148例,马萨诸塞大学21例)在DAE中发现至少1例SBML。最常见的表现为缺铁性贫血/出血(73.3%)和影像学异常(33.6%)。35%的患者在确诊前症状已经持续了一年多。大多数患者(71.6%)在DAE前接受了视频胶囊内窥镜检查(VCE),其中84%的检查显示病变。在DAE之前进行的计算机断层扫描(CT)扫描中发现病变的频率较低(48.9%)。大多数病变是在顺行(56%)或逆行(29.8%)双气囊肠镜(DBE)上发现的。最常见的病变表型是粘膜下病变(41.3%)和带梗病变(33%),无梗病变(14.7%)或阻塞/侵袭性病变(11%)的数量要少得多。它们在空肠(46.3%)和回肠(49.5%)中同样常见。绝大多数病变在10 ~ 20mm之间(47%),但大于20mm的占22.1%。最常见的组织学为神经内分泌肿瘤(NETs, 20.6%)和错构瘤(错构瘤,20.6%)。原发性小肠腺癌是罕见的,仅占病变的5%。大多数息肉(78.4%)为散发性,21.7%与息肉病或遗传性癌症综合征相关,最常见的是Peutz-Jeghers综合征(18.3%)。DAE后,37.6%的患者建议进行手术切除,48%的患者建议进行内镜监测或因组织学良性或内镜切除成功而无需进一步治疗。结论:在这项多中心回顾性研究中,我们发现smml更可能是散发性的,而不是综合征性的,大小中等,有带梗或粘膜下。NETs和错构瘤占主导地位,症状,最常见的贫血,可在诊断前一年以上出现。接近一半的病变不需要进一步干预或只需要内窥镜监测。
Clinical Features and Management of Small Bowel Masses Detected During Device-Assisted Enteroscopy: A Multi-Center Experience.
Background: Small bowel mass lesions (SBMLs) are rare, span a range of different histologies and phenotypes, and our understanding of them is limited. Some lesions occur in patients with recognized polyposis syndromes and others arise sporadically. The current literature regarding SBMLs is limited to small retrospective studies, case reports, and small case series. This large multi-center study aims to understand the various clinical presentations, histologies and management options for SBMLs.
Methods: After obtaining Institutional Review Board (IRB) approval, electronic records were used to identify all device-assisted enteroscopy (DAE) performed for luminal small bowel evaluation in adult patients at three US referral centers (Duke, LSU and UMass) from January 1, 2014, to October 1, 2020. We identified all patients within this cohort in whom a SBML was detected. Using a focused electronic medical record chart review, we collected patient, procedure, and lesion-related data and used descriptive statistics to explore relationships between these data and outcomes.
Results: A total of 218 patients (49 at Duke, 148 at LSU, and 21 at UMass) in this cohort had at least one SBML found on DAE. The most common presenting symptoms were iron-deficiency anemia/bleeding (73.3%) and abnormal imaging (33.6%). Thirty-five percent of patients had symptoms for more than a year prior to their diagnosis. Most patients (71.6%) underwent video capsule endoscopy (VCE) prior to DAE and 84% of these exams showed the lesion. The lesion was seen less frequently (48.9%) on computed tomography (CT) scan performed prior to DAE. The majority of lesions were found on antegrade (56%) or retrograde (29.8%) double-balloon enteroscopy (DBE). The most common lesion phenotypes were submucosal (41.3%) and pedunculated (33%) with a much smaller number being sessile (14.7%) or obstructing/invasive (11%). They were found equally as commonly in the jejunum (46.3%) and ileum (49.5%). Most lesions were 10 - 20 mm in size (47%) but 22.1% were larger than 20 mm. The most common histologies were neuroendocrine tumors (NETs, 20.6%) and hamartomas (20.6%). Primary adenocarcinoma of the small bowel was rare, constituting only 5% of lesions. The majority of polyps (78.4%) were sporadic, compared to 21.7% associated with a polyposis or hereditary cancer syndrome, most commonly Peutz-Jeghers syndrome (18.3%). After DAE, 37.6% were advised to undergo surgical resection and 48% were advised to undergo endoscopic surveillance or no further management because of benign histology or successful endoscopic resection.
Conclusions: In this multi-center retrospective study we found that SBMLs are more likely to be sporadic than syndromic, medium in size and either pedunculated or submucosal. NETs and hamartomas predominated and symptoms, most commonly anemia, can be present for more than a year prior to diagnosis. Close to one half of lesions required either no further intervention or only endoscopic surveillance.