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Solitary Peutz-Jeghers Type Hamartomatous Polyp Arising from the Appendix. 阑尾单发Peutz-Jeghers型错构瘤息肉。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000521196
Mariana Sant'Anna, Elisa Gravito-Soares, Marta Gravito-Soares, Sofia Mendes, Pedro Narra Figueiredo
Digestive hamartomatous polyps may be solitary or multiple, the latter often associated with genetic predisposition [1, 2]. Solitary Peutz-Jeghers (PJ)-type hamartomatous polyps represent a rare and distinct entity from the classic PJ syndrome, an autosomal dominant genetic disorder characterized by the development of multiple polyps in the gastrointestinal (GI) tract in association with patches of hyperpigmentation in the mouth, hands and feet [1, 3]. It is important to distinguish these two entities since the latter is associated with a lifetime cumulative risk of up to 93% for development of malignancies (such as colorectal, breast, small bowel, gastric and pancreatic cancers), but the first seems benign in its course. Solitary PJ polyps are diagnosed in patients with an isolated hamartomatous polyp of the GI tract, no familiar history of polyposis and no typical phenotype [3]. An 80-year-old man with a history of sigmoidectomy due to an obstructive T2N0M0 colorectal cancer underwent a surveillance thoracoabdominopelvic CT scan showing a voluminous endoluminal polyp at the caecum (Fig. 1). He was referred to our reference centre for colonoscopy. A 4-cm diameter pedunculated and congestive polyp was identified with a short and thick stalk arising from the appendiceal orifice. We proceeded to its en bloc resection using a 25-mm oval diathermic snare after stalk injection with diluted adrenaline 1:10,000, normal saline and methylene blue with polyp recovery for histology (Fig. 2a–c, 3a). The polyp was confirmed to be a hamartomatous polyp of the PJ type (R0 resection) with arborizing pattern of vascularized smooth-muscle tissue axes covered by elongated veliform crypts and occasional intraluminal necrosis with no dysplasia (Fig. 3b). The patient had no typical manifestations of PJ syndrome or family history. His follow-up showed no complications related to the procedure, including bleeding or acute appendicitis (prophylactic antibiotic was not used). Solitary PJ-type hamartomatous polyps of the GI tract are rare, and appendiceal location is even rarer. Accord-
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引用次数: 0
Small Bowel Adenocarcinoma in a Patient with Crohn's Disease: The Role of Balloon-Assisted Enteroscopy. 克罗恩病患者的小肠腺癌:气球辅助肠镜检查的作用。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000520906
Emanuel Dias, Miguel Mascarenhas Saraiva, Francisco Moreira, Hélder Cardoso, Guilherme Macedo

Introduction: Small bowel adenocarcinoma is a rare but well-known complication of Crohn's disease. Diagnosis can be challenging, as clinical presentation may mimic an exacerbation of Crohn's disease and imaging findings may be indistinguishable from benign strictures. The result is that the majority of cases are diagnosed at the time of operation or postoperatively at an advanced stage.

Case presentation: A 48-year-old male with a previous 20-year history of ileal stenosing Crohn's disease presented with iron deficiency anemia. The patient reported melena approximately 1 month earlier but was currently asymptomatic. There were no other laboratory abnormalities. Anemia was refractory to intravenous iron replacement. The patient underwent computerized tomography enterography, which revealed multiple ileal strictures with features suggesting underlying inflammation and an area of sacculation with circumferential thickening of adjacent bowel loops. Therefore, the patient underwent retrograde balloon-assisted small bowel enteroscopy, where an area of irregular mucosa and ulceration was found at the region of ileo-ileal anastomosis. Biopsies were performed and histopathological examination revealed tubular adenocarcinoma infiltrating the muscularis mucosae. The patient underwent right hemicolectomy plus segmental enterectomy of the anastomotic region where the neoplasia was located. After 2 months, he is asymptomatic and there is no evidence of recurrence.

Discussion: This case demonstrates that small bowel adenocarcinoma may have a subtle clinical presentation and that computed tomography enterography may not be accurate enough to distinguish benign from malignant strictures. Clinicians must, therefore, maintain a high index of suspicion for this complication in patients with long-standing small bowel Crohn's disease. In this setting, balloon-assisted enteroscopy may be a useful tool when there is raised concern for malignancy, and it is expected that its more widespread use could contribute to an earlier diagnosis of this severe complication.

小肠腺癌是一种罕见但众所周知的克罗恩病并发症。诊断可能具有挑战性,因为临床表现可能模仿克罗恩病的恶化,影像学表现可能与良性狭窄难以区分。结果是,大多数病例在手术时或术后晚期被诊断出来。病例介绍:48岁男性,既往有20年回肠狭窄史,克罗恩病表现为缺铁性贫血。患者约1个月前报告黑黑,但目前无症状。没有其他实验室异常。贫血对静脉补铁是难治性的。患者接受了计算机断层肠摄影检查,发现多处回肠狭窄,表现为潜在的炎症和囊性结缔组织,邻近肠袢呈周向增厚。因此,患者行逆行气囊辅助小肠镜检查,发现回肠-回肠吻合区黏膜不规则及溃疡。活检及病理检查显示管状腺癌浸润粘膜肌层。患者行右半结肠切除术加肿瘤所在吻合区节段性肠切除术。2个月后,患者无症状,无复发迹象。讨论:本病例表明,小肠腺癌可能具有微妙的临床表现,计算机断层扫描肠摄影可能不足以准确区分良性和恶性狭窄。因此,临床医生必须对长期患有小肠克罗恩病的患者的这种并发症保持高度的怀疑。在这种情况下,气球辅助肠镜检查可能是一种有用的工具,当有恶性肿瘤的担忧,并期望其更广泛的使用可以有助于早期诊断这种严重的并发症。
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引用次数: 0
Endoscopic Submucosal Dissection for Subepithelial Tumor Treatment in the Upper Digestive Tract: A Western, Multicenter Study. 内镜下粘膜剥离治疗上消化道上皮下肿瘤:一项西方多中心研究。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000525993
Raffaele Manta, Francesco Paolo Zito, Francesco Pugliese, Angelo Caruso, Santi Mangiafico, Alessandra D'Alessandro, Danilo Castellani, Ugo Germani, Massimiliano Mutignani, Rita Luisa Conigliaro, Luca Reggiani Bonetti, Takahisa Matsuda, Vincenzo De Francesco, Angelo Zullo, Giuseppe Galloro

Background/aims: Endoscopic submucosal dissection (ESD) has been proposed for removal of gastrointestinal subepithelial tumors (GI-SETs), but data are still scanty. This study aimed to report a case series from a western country.

Patients and methods: Data of patients with upper GI-SETs suitable for ESD removal observed in 4 centers were retrospectively reviewed. Before endoscopic procedure, the lesion was characterized by endosonographic evaluation, histology, and CT scan. The en bloc resection and the R0 resection rates were calculated, as well as incidence of complications, and the 1-year follow-up was reported.

Results: Data of 84 patients with esophageal (N = 13), gastric (N = 61), and duodenal (N = 10) GI-SETs were collected. The mean diameter of lesions was 26 mm (range: 12-110 mm). There were 17 gastrointestinal stromal tumors, 12 neuroendocrine tumors, 35 leiomyomas, 18 lipomas, and 2 hamartomas. En bloc and R0 resection were achieved in 83 (98.8%) and in 80 (95.2%) patients, respectively. Overall, a complication occurred in 11 (13.1%) patients, including bleeding (N = 7) and perforation (N = 4). Endoscopic approach was successful in all bleedings, but 1 patient who required radiological embolization, and in 2 perforations, while surgery was performed in the other patients. Overall, a surgical approach was eventually needed in 5 (5.9%), including 3 in whom R0 resection failed and 2 with perforation.

Conclusions: Our study found that ESD may be an effective and safe alternative to surgical intervention for both benign and localized malignant GI-SETs.

背景/目的:内镜下粘膜剥离(ESD)已被提出用于胃肠道上皮下肿瘤(GI-SETs)的切除,但数据仍然很少。本研究旨在报道一个西方国家的病例系列。患者和方法:回顾性分析4个中心观察到的适合ESD移除的上GI-SETs患者的资料。在内窥镜手术前,病变通过超声评估、组织学和CT扫描进行表征。计算整体切除率、R0切除率及并发症发生率,并报道1年随访。结果:收集84例食管(N = 13)、胃(N = 61)、十二指肠(N = 10) GI-SETs数据。病灶直径平均26 mm(范围12 ~ 110 mm)。胃肠道间质瘤17例,神经内分泌瘤12例,平滑肌瘤35例,脂肪瘤18例,错构瘤2例。整体切除83例(98.8%),R0切除80例(95.2%)。总体而言,11例(13.1%)患者出现并发症,包括出血(N = 7)和穿孔(N = 4)。内镜下入路在所有出血中都成功,但1例患者需要放射栓塞,2例穿孔,而其他患者进行了手术。总体而言,5例(5.9%)最终需要手术入路,其中3例R0切除术失败,2例穿孔。结论:我们的研究发现,对于良性和局部恶性GI-SETs, ESD可能是一种有效且安全的手术干预方法。
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引用次数: 1
Erratum. 勘误表。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000528361

[This corrects the article DOI: 10.1159/000525994.].

[这更正了文章DOI: 10.1159/000525994。]
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000528333

[This corrects the article DOI: 10.1159/000524060.].

[这更正了文章DOI: 10.1159/000524060]。
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000528359

[This corrects the article DOI: 10.1159/000525993.].

[此更正文章DOI: 10.1159/000525993.]。
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000528340

[This corrects the article DOI: 10.1159/000525964.].

[这更正了文章DOI: 10.1159/000525964。]
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000528362

[This corrects the article DOI: 10.1159/000526032.].

[此更正文章DOI: 10.1159/000526032.]。
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000528337

[This corrects the article DOI: 10.1159/000525809.].

[这更正了文章DOI: 10.1159/000525809.]。
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-03-01 DOI: 10.1159/000528366

[This corrects the article DOI: 10.1159/000526126.].

[此更正文章DOI: 10.1159/000526126.]。
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GE Portuguese Journal of Gastroenterology
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