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Endoscopic Retrograde Cholangiopancreatography on Pediatric Patients: Experience of a Portuguese Adult Gastroenterology Department 内窥镜逆行胆管造影对儿科患者:葡萄牙成人消化内科的经验
Q3 Medicine Pub Date : 2023-03-08 DOI: 10.1159/000529090
Rita Ornelas Saraiva, Verónica Pavão Borges, Mário Jorge Silva, Rafaela Loureiro, Tiago Capela, Gonçalo Ramos, Jorge Canena, António Mateus Dias, Rui Alves, João Coimbra
Introduction: Experience with endoscopic retrograde cholangiopancreatography (ERCP) in the pediatric population is limited. Few medical centers have experts specifically trained in pediatric therapeutic endoscopy. As a result, patients are generally referred to adult endoscopists with high experience in the procedure. The aim of this study was to characterize the experience of an adult endoscopy unit with ERCP on pediatric patients, with a special focus on very young patients. Methods: We retrospectively analyzed indications, technical success rate, final clinical diagnosis, and complications of ERCPs in children <18 years at our tertiary referral hospital center between January 1994 and June 2022. Results: Sixty-five ERCPs were performed on 57 children with a median age of 13 years (range 1–17 years). Eleven ERCPs were performed on 9 patients up to 5 years old. Indications for ERCP were as follows: biliary obstruction (n = 40), mainly due to choledocholithiasis, lithiasic acute pancreatitis (n = 19), recurrent pancreatitis (n = 3), stent extraction (n = 2), and post-operative biliary fistula (n = 1). The cannulation success rate was 95.1%. Therapeutic interventions were performed in 79% of ERCP. All patients were followed up as inpatients. Complications were recorded in two procedures (3.1%), and no procedure-related mortality occurred. Conclusion: In our experience, ERCP in children can be safely performed with high success rates by advanced adult-trained expert endoscopists at a high-volume center.
& lt; b> & lt; i>简介:& lt; / i> & lt; / b>内窥镜逆行胆管造影术(ERCP)在儿科人群中的经验是有限的。很少有医疗中心有专门训练儿科治疗性内窥镜的专家。因此,患者通常被推荐给在手术方面经验丰富的成人内窥镜医师。本研究的目的是描述成人内窥镜单元对儿童患者进行ERCP的经验,特别关注非常年轻的患者。& lt; b> & lt; i>方法:& lt; / i> & lt; / b>我们回顾性分析了1994年1月至2022年6月在我们三级转诊医院中心进行的18年儿童ercp的适应症、技术成功率、最终临床诊断和并发症。& lt; b> & lt; i>结果:& lt; / i> & lt; / b>对57名中位年龄13岁(范围1-17岁)的儿童进行65例ercp。对9例5岁以下的患者进行了11次ercp。ERCP的适应症如下:胆道梗阻(<i>n</i>= 40),主要因胆总管结石、结石性急性胰腺炎(<i>n</i>= 19),复发性胰腺炎(<i>n</i>= 3),支架拔出(<i>n</i>= 2),术后胆瘘(<i>n</i>= 1),插管成功率为95.1%。在79%的ERCP中进行了治疗干预。所有患者均作为住院患者随访。两例手术发生并发症(3.1%),无手术相关死亡发生。& lt; b> & lt; i>结论:& lt; / i> & lt; / b>根据我们的经验,在高容量中心,由受过高级成人培训的内窥镜专家安全且成功率高的情况下,可以对儿童进行ERCP。
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引用次数: 0
Current Approach to Dysphagia: A Review Focusing on Esophageal Motility Disorders and Their Treatment. 吞咽困难的当前治疗方法:以食管运动障碍及其治疗为重点的综述》(Current Approach to Dysphagia: A Review Focusing on Esophageal Motility Disorders and Their Treatment)。
IF 0.9 Q3 Medicine Pub Date : 2023-03-08 eCollection Date: 2023-12-01 DOI: 10.1159/000529428
André Mascarenhas, Rui Mendo, Catarina O'Neill, Ana Rita Franco, Raquel Mendes, Inês Simão, José Pedro Rodrigues

Background: Dysphagia is a prevalent condition which may severely impact the patient's quality of life. However, there are still lacking standardized therapeutic options for esophageal motility disorders.

Summary: Dysphagia is defined as a subjective sensation of difficulty swallowing which can result from oropharyngeal or esophageal etiologies. Regarding esophageal dysphagia, after excluding structural causes and esophageal mucosal lesions, high-resolution manometry (HRM) is the gold standard for the diagnosis of esophageal motility disorders. HRM has not only improved the sensitivity for detecting achalasia but has also expanded our understanding of spastic and hypomotility disorders of the esophageal body. The Chicago Classification v4.0 uses a hierarchical approach and provides a standardized diagnosis of esophageal motility disorders, allowing a tailored therapeutic approach. Dysphagia is often a long-term health problem that broadly impacts health and well-being and leads to physical and psychosocial disability, namely, malnutrition and aspiration pneumonia, as well as social isolation, depression, and anxiety. Apart from achalasia, most esophageal motility disorders tend to have a benign long-term course with symptoms of dysphagia and noncardiac chest pain that can improve significantly over time. Patient-reported outcomes (PROs) are self-assessment tools that capture the patients' illness experience and help providers better understand symptoms from the patients' perspective. Therefore, PROs have a critical role in providing patient-centered care.

Key messages: Motility disorders should be ruled out in the presence of nonobstructive esophageal dysphagia, and treatment options should be considered according to the severity of symptoms reported by the patient.

背景:吞咽困难是一种普遍存在的疾病,可能严重影响患者的生活质量。摘要:吞咽困难的定义是吞咽困难的主观感觉,可由口咽或食道病因引起。关于食管吞咽困难,在排除结构性原因和食管粘膜病变后,高分辨率测压法(HRM)是诊断食管运动障碍的金标准。高分辨率测压法不仅提高了检测贲门失弛缓症的灵敏度,还扩展了我们对食管痉挛和食管运动功能减退疾病的认识。芝加哥分类法》v4.0 采用分层方法,为食管运动障碍提供了标准化诊断,从而可以采取有针对性的治疗方法。吞咽困难通常是一个长期的健康问题,会广泛影响健康和幸福,并导致身体和心理残疾,即营养不良和吸入性肺炎,以及社会隔离、抑郁和焦虑。除贲门失弛缓症外,大多数食管运动障碍的长期病程往往是良性的,吞咽困难和非心源性胸痛的症状会随着时间的推移而明显改善。患者报告结果(PROs)是一种自我评估工具,可记录患者的患病经历,帮助医疗服务提供者从患者的角度更好地了解症状。因此,PROs 在提供以患者为中心的护理方面发挥着至关重要的作用:关键信息:出现非梗阻性食管吞咽困难时应排除运动障碍,并根据患者报告的症状严重程度考虑治疗方案。
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引用次数: 0
Transvenous Obliteration Procedure in the Management of Parastomal Variceal Bleeding: A Case Report. 经静脉闭塞术治疗造口旁静脉曲张出血1例。
IF 0.9 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.1159/000521325
João Estorninho, Pedro Patrão, Maria José Temido, David Perdigoto, Pedro Figueiredo, Paulo Donato

Introduction: Parastomal variceal bleeding (PVB) is a recognized complication of ostomized patients in the presence of portal hypertension. However, since there are few reported cases, a therapeutic algorithm has not yet been established.

Case presentation: A 63-year-old man, who had undergone a definitive colostomy, recurrently presented to the emergency department hemorrhage of bright red blood from his colostomy bag, initially assumed to be caused by stoma trauma. Accordingly, temporary success on local approaches such as direct compression, silver nitrate application and suture ligation was achieved. However, bleeding recurred, requiring transfusion of red blood cell concentrate and hospitalization. The patient's evaluation showed chronic liver disease with massive collateral circulation, particularly at the colostomy site. After a PVB with associated hypovolemic shock, the patient was submitted to a balloon-occluded retrograde transvenous obliteration (BRTO) procedure which stopped the bleeding successfully. The patient was subsequently proposed for a transjugular intrahepatic portosystemic shunt (TIPS) conjugated with percutaneous transhepatic obliteration (PTO). After an initial refusal by the patient, a new episode of self-limited PVB resulted in execution of the procedure. Four months later, in a routine consultation, the patient presented with grade II hepatic encephalopathy, successfully treated with medical therapy. After a 9-month follow-up, he remained clinically well and without further episodes of PVB or other adverse effects.

Discussion: This report highlights the importance of a high index of suspicion when dealing with significant stomal hemorrhage. Portal hypertension as an etiology of this entity may compel to a specific approach to prevent recurrence of bleeding, including conjugation of endovascular procedures. The authors pre-sent a case of PVB, initially submitted to a variety of treatment options including BRTO, which was successfully addressed with conjugated treatment of TIPS and PTO.

简介:造口旁静脉曲张出血(PVB)是门静脉高压症患者的一个公认的并发症。然而,由于报告的病例很少,治疗算法尚未建立。病例介绍:一名63岁男性,接受了明确的结肠造口术,反复出现结肠造口袋出血鲜红色血液,最初认为是由造口外伤引起的。因此,局部入路如直接压迫、硝酸银应用和缝合结扎取得了暂时的成功。然而,出血复发,需要输血浓缩红细胞和住院治疗。患者的评估显示慢性肝病伴大量侧支循环,特别是在结肠造口部位。在PVB伴低血容量性休克后,患者接受了球囊闭塞逆行经静脉闭塞术(BRTO),成功止血。患者随后被建议进行经颈静脉肝内门静脉系统分流术(TIPS)结合经皮经肝闭塞术(PTO)。在患者最初拒绝后,自限性PVB的新发作导致了手术的执行。四个月后,在一次常规会诊中,患者表现为II级肝性脑病,经药物治疗成功。随访9个月后,患者临床状态良好,无PVB发作或其他不良反应。讨论:本报告强调了在处理显著口出血时高度怀疑的重要性。门静脉高压症作为这种疾病的病因,可能需要采取特殊的方法来防止出血复发,包括血管内手术的结合。作者提出了一个PVB病例,最初提交了包括BRTO在内的多种治疗方案,通过TIPS和PTO的结合治疗成功地解决了这个问题。
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.1159/000528365

[This corrects the article DOI: 10.1159/000526125.].

[此更正文章DOI: 10.1159/000526125.]。
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.1159/000528334

[This corrects the article DOI: 10.1159/000524062.].

[这更正了文章DOI: 10.1159/000524062.]。
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引用次数: 0
Erratum. 勘误表。
IF 0.9 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.1159/000528332

[This corrects the article DOI: 10.1159/000523773.].

[这更正了文章DOI: 10.1159/000523773]。
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引用次数: 0
Long-Term Intestinal Failure and Home Parenteral Support: A Single Center Experience. 长期肠衰竭和家庭肠外支持:单中心经验。
IF 0.9 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.1159/000522161
Mariana Brito, Mafalda Padinha, Sandra Carlos, Cátia Oliveira, Ana Paula Santos, Gonçalo Nunes, Carla Adriana Santos, Jorge Fonseca

Introduction: Home parenteral nutrition (HPN) and/or home parenteral hydration (HPH) are the gold-standard treatment for patients with long-term intestinal failure (IF). The authors aimed to assess the impact of HPN/HPH on nutritional status and survival of long-term IF patients, as well as HPN/HPH-related complications.

Methods: This was a retrospective study including IF patients under HPN/HPH followed in a single large tertiary Portuguese hospital. The data collected included demographics, underlying conditions, anatomical characteristics, type and duration of parenteral support, IF functional, pathophysiological, and clinical classifications, body mass index (BMI) at the beginning and end of follow-up, complications/hospitalizations, current patient status (deceased, alive with HPN/HPH, and alive without HPN/HPH), and cause of death. Survival after HPN/HPH beginning, until death or August 2021, was recorded in months.

Results: Overall 13 patients were included (53.9% female, mean age 63.46 years), and 84.6% of patients presented type III IF and 15.4% type II. Short bowel syndrome caused 76.9% of IF. Nine patients received HPN and 4 HPH. Eight patients (61.5%) were underweight at the beginning of HPN/HPH. At the end of follow-up, 4 patients were alive without HPN/HPH, 4 maintained HPN/HPH, and 5 died. All patients improved their BMI (mean initial BMI 18.9 vs. 23.5 at the end, p < 0.001). Eight patients (61.5%) were hospitalized due to catheter-related complications, mainly infectious (mean hospitalization episodes 2.25, mean hospital stay of 24.5 days). No deaths were related to HPN/HPH.

Conclusion: HPN/HPH significantly improved IF patients' BMI. HPN/HPH-related hospitalizations were common, however causing no deaths, reinforcing that HPN/HPH is an adequate and safe therapy for long-term IF patients.

家庭肠外营养(HPN)和/或家庭肠外水化(HPH)是长期肠衰竭(IF)患者的金标准治疗方法。作者旨在评估HPN/HPH对长期IF患者营养状况和生存的影响,以及HPN/HPH相关并发症。方法:这是一项回顾性研究,包括在葡萄牙一家大型三级医院接受HPN/HPH治疗的IF患者。收集的数据包括人口统计学、基础条件、解剖特征、肠外支持的类型和持续时间、IF功能、病理生理和临床分类、随访开始和结束时的体重指数(BMI)、并发症/住院情况、当前患者状态(死亡、伴HPN/HPH存活、无HPN/HPH存活)和死亡原因。以月为单位记录HPN/HPH开始后的生存,直到死亡或2021年8月。结果:共纳入13例患者(女性53.9%,平均年龄63.46岁),其中84.6%的患者为III型IF, 15.4%为II型IF。76.9%的IF由短肠综合征引起。9例患者接受HPN治疗,4例接受HPH治疗。8例(61.5%)患者在HPN/HPH开始时体重过轻。随访结束时,4例患者无HPN/HPH, 4例患者维持HPN/HPH, 5例死亡。所有患者的BMI均有所改善(初始平均BMI为18.9,结束时为23.5,p < 0.001)。8例(61.5%)患者因导管相关并发症住院,以感染性并发症为主(平均住院次数2.25次,平均住院时间24.5 d)。没有与HPN/HPH相关的死亡。结论:HPN/HPH可显著改善IF患者的BMI。与HPN/HPH相关的住院治疗很常见,但没有造成死亡,这加强了HPN/HPH对长期IF患者来说是一种足够和安全的治疗方法。
{"title":"Long-Term Intestinal Failure and Home Parenteral Support: A Single Center Experience.","authors":"Mariana Brito,&nbsp;Mafalda Padinha,&nbsp;Sandra Carlos,&nbsp;Cátia Oliveira,&nbsp;Ana Paula Santos,&nbsp;Gonçalo Nunes,&nbsp;Carla Adriana Santos,&nbsp;Jorge Fonseca","doi":"10.1159/000522161","DOIUrl":"https://doi.org/10.1159/000522161","url":null,"abstract":"<p><strong>Introduction: </strong>Home parenteral nutrition (HPN) and/or home parenteral hydration (HPH) are the gold-standard treatment for patients with long-term intestinal failure (IF). The authors aimed to assess the impact of HPN/HPH on nutritional status and survival of long-term IF patients, as well as HPN/HPH-related complications.</p><p><strong>Methods: </strong>This was a retrospective study including IF patients under HPN/HPH followed in a single large tertiary Portuguese hospital. The data collected included demographics, underlying conditions, anatomical characteristics, type and duration of parenteral support, IF functional, pathophysiological, and clinical classifications, body mass index (BMI) at the beginning and end of follow-up, complications/hospitalizations, current patient status (deceased, alive with HPN/HPH, and alive without HPN/HPH), and cause of death. Survival after HPN/HPH beginning, until death or August 2021, was recorded in months.</p><p><strong>Results: </strong>Overall 13 patients were included (53.9% female, mean age 63.46 years), and 84.6% of patients presented type III IF and 15.4% type II. Short bowel syndrome caused 76.9% of IF. Nine patients received HPN and 4 HPH. Eight patients (61.5%) were underweight at the beginning of HPN/HPH. At the end of follow-up, 4 patients were alive without HPN/HPH, 4 maintained HPN/HPH, and 5 died. All patients improved their BMI (mean initial BMI 18.9 vs. 23.5 at the end, <i>p</i> < 0.001). Eight patients (61.5%) were hospitalized due to catheter-related complications, mainly infectious (mean hospitalization episodes 2.25, mean hospital stay of 24.5 days). No deaths were related to HPN/HPH.</p><p><strong>Conclusion: </strong>HPN/HPH significantly improved IF patients' BMI. HPN/HPH-related hospitalizations were common, however causing no deaths, reinforcing that HPN/HPH is an adequate and safe therapy for long-term IF patients.</p>","PeriodicalId":51838,"journal":{"name":"GE Portuguese Journal of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/b6/66/pjg-0030-0127.PMC10050871.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9241845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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 Q3 Medicine 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-
{"title":"Solitary Peutz-Jeghers Type Hamartomatous Polyp Arising from the Appendix.","authors":"Mariana Sant'Anna,&nbsp;Elisa Gravito-Soares,&nbsp;Marta Gravito-Soares,&nbsp;Sofia Mendes,&nbsp;Pedro Narra Figueiredo","doi":"10.1159/000521196","DOIUrl":"https://doi.org/10.1159/000521196","url":null,"abstract":"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-","PeriodicalId":51838,"journal":{"name":"GE Portuguese Journal of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/84/72/pjg-0030-0156.PMC10050839.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9241699","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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 Q3 Medicine 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。
{"title":"Small Bowel Adenocarcinoma in a Patient with Crohn's Disease: The Role of Balloon-Assisted Enteroscopy.","authors":"Emanuel Dias,&nbsp;Miguel Mascarenhas Saraiva,&nbsp;Francisco Moreira,&nbsp;Hélder Cardoso,&nbsp;Guilherme Macedo","doi":"10.1159/000520906","DOIUrl":"https://doi.org/10.1159/000520906","url":null,"abstract":"<p><strong>Introduction: </strong>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.</p><p><strong>Case presentation: </strong>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.</p><p><strong>Discussion: </strong>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.</p>","PeriodicalId":51838,"journal":{"name":"GE Portuguese Journal of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/18/a9/pjg-0030-0141.PMC10050865.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9241700","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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 Q3 Medicine 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。
{"title":"Endoscopic Submucosal Dissection for Subepithelial Tumor Treatment in the Upper Digestive Tract: A Western, Multicenter Study.","authors":"Raffaele Manta,&nbsp;Francesco Paolo Zito,&nbsp;Francesco Pugliese,&nbsp;Angelo Caruso,&nbsp;Santi Mangiafico,&nbsp;Alessandra D'Alessandro,&nbsp;Danilo Castellani,&nbsp;Ugo Germani,&nbsp;Massimiliano Mutignani,&nbsp;Rita Luisa Conigliaro,&nbsp;Luca Reggiani Bonetti,&nbsp;Takahisa Matsuda,&nbsp;Vincenzo De Francesco,&nbsp;Angelo Zullo,&nbsp;Giuseppe Galloro","doi":"10.1159/000525993","DOIUrl":"https://doi.org/10.1159/000525993","url":null,"abstract":"<p><strong>Background/aims: </strong>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.</p><p><strong>Patients and methods: </strong>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 <i>en bloc</i> resection and the R0 resection rates were calculated, as well as incidence of complications, and the 1-year follow-up was reported.</p><p><strong>Results: </strong>Data of 84 patients with esophageal (<i>N</i> = 13), gastric (<i>N</i> = 61), and duodenal (<i>N</i> = 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. <i>En bloc</i> 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 (<i>N</i> = 7) and perforation (<i>N</i> = 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.</p><p><strong>Conclusions: </strong>Our study found that ESD may be an effective and safe alternative to surgical intervention for both benign and localized malignant GI-SETs.</p>","PeriodicalId":51838,"journal":{"name":"GE Portuguese Journal of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a0/3e/pjg-0030-0115.PMC10050838.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9241702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
GE Portuguese Journal of Gastroenterology
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