首页 > 最新文献

Acta gastro-enterologica Belgica最新文献

英文 中文
An unusual cause of abdominal pain: spontaneous bilateral adrenal hemorrhage. 腹痛的一个不寻常原因:自发性双侧肾上腺出血。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.11251
A Rodriguez Tebar, J Panza-Nduli, B Gubin, P-A Rogghe, P Oriot

Bilateral adrenal hemorrhage (BAH) is a rare condition that can lead to acute adrenal insufficiency and death if not recognized and treated promptly. We report the case of a 30-year-old male who presented to the emergency department with acute abdominal pain, nausea, and vomiting. On emergency room admission, the first abdominal CT revealed normal adrenal glands without enlargement, but with the development of hypotension and hypoglycemia, a second CT performed four days later showed enlargement due to hemorrhage in both adrenals. The diagnosis of BAH associated with acute adrenal insufficiency was retained. Prompt treatment with intravenous and oral corticosteroids resulted in successful conservative management. We describe the clinical, biological, radiological and etiological features of this condition based on a review of the literature.

双侧肾上腺出血(BAH)是一种罕见的情况,如果不及时识别和治疗,可能导致急性肾上腺功能不全和死亡。我们报告了一例30岁男性,因急性腹痛、恶心和呕吐到急诊科就诊。急诊室入院时,第一次腹部CT显示肾上腺正常,没有增大,但随着低血压和低血糖的发展,四天后进行的第二次CT显示由于两个肾上腺出血而增大。保留了BAH与急性肾上腺功能不全相关的诊断。静脉和口服皮质类固醇的及时治疗使保守治疗成功。我们在回顾文献的基础上描述了这种情况的临床、生物学、放射学和病因特征。
{"title":"An unusual cause of abdominal pain: spontaneous bilateral adrenal hemorrhage.","authors":"A Rodriguez Tebar,&nbsp;J Panza-Nduli,&nbsp;B Gubin,&nbsp;P-A Rogghe,&nbsp;P Oriot","doi":"10.51821/86.3.11251","DOIUrl":"10.51821/86.3.11251","url":null,"abstract":"<p><p>Bilateral adrenal hemorrhage (BAH) is a rare condition that can lead to acute adrenal insufficiency and death if not recognized and treated promptly. We report the case of a 30-year-old male who presented to the emergency department with acute abdominal pain, nausea, and vomiting. On emergency room admission, the first abdominal CT revealed normal adrenal glands without enlargement, but with the development of hypotension and hypoglycemia, a second CT performed four days later showed enlargement due to hemorrhage in both adrenals. The diagnosis of BAH associated with acute adrenal insufficiency was retained. Prompt treatment with intravenous and oral corticosteroids resulted in successful conservative management. We describe the clinical, biological, radiological and etiological features of this condition based on a review of the literature.</p>","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"495-498"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181777","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Local and systemic autoimmune manifestations linked to hepatitis A infection. 与甲型肝炎感染相关的局部和全身自身免疫表现。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.11299
M Doulberis, A Papaefthymiou, S A Polyzos, E Vardaka, M Tzitiridou-Chatzopoulou, D Chatzopoulos, A Koffas, V Papadopoulos, F Kyrailidi, J Kountouras

Hepatitis A virus (HAV) represents a global burdening infectious agent causing in the majority of cases a self-limiting acute icteric syndrome, the outcome is related to the hepatic substrate and the potential pre-existing damage, whereas a plethora of extra-hepatic manifestations has also been reported. Despite the absence of post- HAV chronicity it has been associated with an additional burden on existing chronic liver diseases. Moreover, the induced immune response and the antigenic molecular mimicry are considered as triggering factors of autoimmunity with regional and distal impact. Diseases such as autoimmune hepatitis, Guillain-Barré syndrome, rheumatoid arthritis, Still's syndrome, Henoch-Schönlein purpura, autoimmune hemolytic anemia, antiphospholipid syndrome, systematic lupus erythematosus or cryoglobulinemic vasculitis have been described in patients with HAV infection. Although the exact mechanisms remain unclear, this review aims to accumulate and clarify the pathways related to this linkage.

甲型肝炎病毒(HAV)是一种全球性的负担传染源,在大多数情况下会导致自限性急性黄疸综合征,其结果与肝脏基质和潜在的预先存在的损伤有关,而也有大量肝外表现的报道。尽管没有甲型肝炎后的慢性病,但它与现有慢性肝病的额外负担有关。此外,诱导的免疫反应和抗原分子模拟被认为是具有区域和远端影响的自身免疫的触发因素。HAV感染患者中出现了自身免疫性肝炎、格林-巴利综合征、类风湿性关节炎、斯蒂尔综合征、过敏性紫癜、自身免疫性溶血性贫血、抗磷脂综合征、系统性红斑狼疮或冷球蛋白血症血管炎等疾病。尽管确切的机制尚不清楚,但本综述旨在积累和阐明与这种联系相关的途径。
{"title":"Local and systemic autoimmune manifestations linked to hepatitis A infection.","authors":"M Doulberis,&nbsp;A Papaefthymiou,&nbsp;S A Polyzos,&nbsp;E Vardaka,&nbsp;M Tzitiridou-Chatzopoulou,&nbsp;D Chatzopoulos,&nbsp;A Koffas,&nbsp;V Papadopoulos,&nbsp;F Kyrailidi,&nbsp;J Kountouras","doi":"10.51821/86.3.11299","DOIUrl":"10.51821/86.3.11299","url":null,"abstract":"<p><p>Hepatitis A virus (HAV) represents a global burdening infectious agent causing in the majority of cases a self-limiting acute icteric syndrome, the outcome is related to the hepatic substrate and the potential pre-existing damage, whereas a plethora of extra-hepatic manifestations has also been reported. Despite the absence of post- HAV chronicity it has been associated with an additional burden on existing chronic liver diseases. Moreover, the induced immune response and the antigenic molecular mimicry are considered as triggering factors of autoimmunity with regional and distal impact. Diseases such as autoimmune hepatitis, Guillain-Barré syndrome, rheumatoid arthritis, Still's syndrome, Henoch-Schönlein purpura, autoimmune hemolytic anemia, antiphospholipid syndrome, systematic lupus erythematosus or cryoglobulinemic vasculitis have been described in patients with HAV infection. Although the exact mechanisms remain unclear, this review aims to accumulate and clarify the pathways related to this linkage.</p>","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"429-436"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181700","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Melanoma of the gallbladder. 胆囊黑色素瘤。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.12020
A Boca, N Bletard, R Materne
An 80-year-old man, with no medical history, was referred to the gastroenterologist due to cholestasis and altered general condition. Physical examination revealed mild abdominal tenderness in the right hypochondrium, with no other clinical signs. Laboratory examinations showed a cholestasis (gamma-glutamyl transferase: 160 U/L and alkaline phosphatase: 120 U/L) and an elevated CRP level of 25 mg/L. Abdominal MRI was performed (Fig 1, Fig 2A). Subsequently, a PET-CT and brain MRI for seizures (Fig. 2B) were realized.
{"title":"Melanoma of the gallbladder.","authors":"A Boca,&nbsp;N Bletard,&nbsp;R Materne","doi":"10.51821/86.3.12020","DOIUrl":"10.51821/86.3.12020","url":null,"abstract":"An 80-year-old man, with no medical history, was referred to the gastroenterologist due to cholestasis and altered general condition. Physical examination revealed mild abdominal tenderness in the right hypochondrium, with no other clinical signs. Laboratory examinations showed a cholestasis (gamma-glutamyl transferase: 160 U/L and alkaline phosphatase: 120 U/L) and an elevated CRP level of 25 mg/L. Abdominal MRI was performed (Fig 1, Fig 2A). Subsequently, a PET-CT and brain MRI for seizures (Fig. 2B) were realized.","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"505-506"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An unusual cause of extrahepatic cholestasis associated with solid liver lesions: a case report. 肝外胆汁淤积合并实体肝病变的一个不寻常原因:一例报告。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.10393
L Caverenne, L Weichselbaum, M Van Hoof, P Deltenre

IgG4-related sclerosing cholangitis is a special type of cholangiopathy often associated with autoimmune pancreatitis. In this article, we report an unusual case of IgG4-SC limited to the common hepatic duct and associated with pseudo tumoral liver lesions, but without evidence of pancreatic involvement. Corticosteroid therapy was rapidly effective and allowed normalization of liver tests.

IgG4相关的硬化性胆管炎是一种特殊类型的胆管疾病,通常与自身免疫性胰腺炎有关。在这篇文章中,我们报告了一例不寻常的IgG4 SC病例,局限于肝总管,并与假肿瘤性肝脏病变有关,但没有胰腺受累的证据。皮质类固醇治疗效果迅速,使肝脏检查正常化。
{"title":"An unusual cause of extrahepatic cholestasis associated with solid liver lesions: a case report.","authors":"L Caverenne,&nbsp;L Weichselbaum,&nbsp;M Van Hoof,&nbsp;P Deltenre","doi":"10.51821/86.3.10393","DOIUrl":"10.51821/86.3.10393","url":null,"abstract":"<p><p>IgG4-related sclerosing cholangitis is a special type of cholangiopathy often associated with autoimmune pancreatitis. In this article, we report an unusual case of IgG4-SC limited to the common hepatic duct and associated with pseudo tumoral liver lesions, but without evidence of pancreatic involvement. Corticosteroid therapy was rapidly effective and allowed normalization of liver tests.</p>","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"490-492"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biliary papillomatosis. 胆道乳头状瘤病。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.11733
F Gelders, M Struyve, H van Malenstein

Biliary papillomatosis (BP) is a rare disorder of the biliary tract characterized by the presence of multiple papillary adenomas spread along the biliary tree. Although benign, it carries a significant risk of malignant transformation. Due to low sensitivity and specificity of conventional radiologic modalities, the diagnosis as well as estimation of disease extent is difficult. Endoscopic ultrasound (EUS) and endoscopic retrograde cholangiopancreaticography (ERCP) are superior although direct peroral cholangioscopy (POC) is currently the most accurate diagnostic method. Mainly because it provides more detailed information and makes targeted histological diagnosis possible. The treatment of biliary papillomatosis consists of surgical resection, liver transplantation (LT) or a combination of both. Unfortunately, the recurrence rate after radical surgery without LT remains high due to the diffuse distribution of the disease.

胆道乳头状瘤病(BP)是一种罕见的胆道疾病,其特征是存在沿胆管树分布的多个乳头状腺瘤。虽然是良性的,但它有恶性转化的重大风险。由于传统放射学方法的敏感性和特异性低,诊断和估计疾病程度都很困难。内镜超声(EUS)和内镜逆行胰胆管造影(ERCP)是优越的,尽管直接经口胆管镜(POC)是目前最准确的诊断方法。主要是因为它提供了更详细的信息,并使有针对性的组织学诊断成为可能。胆道乳头状瘤病的治疗包括手术切除、肝移植或两者结合。不幸的是,由于疾病的弥漫性分布,在没有LT的情况下进行根治性手术后的复发率仍然很高。
{"title":"Biliary papillomatosis.","authors":"F Gelders,&nbsp;M Struyve,&nbsp;H van Malenstein","doi":"10.51821/86.3.11733","DOIUrl":"10.51821/86.3.11733","url":null,"abstract":"<p><p>Biliary papillomatosis (BP) is a rare disorder of the biliary tract characterized by the presence of multiple papillary adenomas spread along the biliary tree. Although benign, it carries a significant risk of malignant transformation. Due to low sensitivity and specificity of conventional radiologic modalities, the diagnosis as well as estimation of disease extent is difficult. Endoscopic ultrasound (EUS) and endoscopic retrograde cholangiopancreaticography (ERCP) are superior although direct peroral cholangioscopy (POC) is currently the most accurate diagnostic method. Mainly because it provides more detailed information and makes targeted histological diagnosis possible. The treatment of biliary papillomatosis consists of surgical resection, liver transplantation (LT) or a combination of both. Unfortunately, the recurrence rate after radical surgery without LT remains high due to the diffuse distribution of the disease.</p>","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"483-485"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181780","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial. 社论
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.12360
C Reenaers, H De Schepper
In this issue several important original papers as well as extensive reviews can be highlighted. The management of pelvic abscesses is usually challenging and the drainage is mandatory to avoid pelvis sepsis. Recently, minimally invasive techniques, including endoscopic ultrasound- guided transrectal drainage have been associated with a high success rates and good safety results (1). Peeters et all retrospectively analysed 17 patients with pelvic abscess and demonstrated a success rate of the technique of 100% defined by a resolution of the abscess. The full details of the technique are described in the original manuscript. In the hepatic section, since the picture of cirrhosis has changed in the last 2 decades with more metabolic dysfunction-associated steatotic liver diseases (2), Kaze et al aimed to assess whether the epidemiological and the clinical course of hepatocellular carcinoma had also changed over the last 25 years. By comparing two cohorts respectively before and after 2005 no major epidemiological changes were found except a higher rate of Alcohol-related HCC in the old cohort compared to the recent cohort. Metabolic dysfunction was similar with 10% in all groups. The review section includes three interesting.
{"title":"Editorial.","authors":"C Reenaers,&nbsp;H De Schepper","doi":"10.51821/86.3.12360","DOIUrl":"10.51821/86.3.12360","url":null,"abstract":"In this issue several important original papers as well as extensive reviews can be highlighted. The management of pelvic abscesses is usually challenging and the drainage is mandatory to avoid pelvis sepsis. Recently, minimally invasive techniques, including endoscopic ultrasound- guided transrectal drainage have been associated with a high success rates and good safety results (1). Peeters et all retrospectively analysed 17 patients with pelvic abscess and demonstrated a success rate of the technique of 100% defined by a resolution of the abscess. The full details of the technique are described in the original manuscript. In the hepatic section, since the picture of cirrhosis has changed in the last 2 decades with more metabolic dysfunction-associated steatotic liver diseases (2), Kaze et al aimed to assess whether the epidemiological and the clinical course of hepatocellular carcinoma had also changed over the last 25 years. By comparing two cohorts respectively before and after 2005 no major epidemiological changes were found except a higher rate of Alcohol-related HCC in the old cohort compared to the recent cohort. Metabolic dysfunction was similar with 10% in all groups. The review section includes three interesting.","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"393"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An unusual cause of portal hypertension. 门静脉高压的一个不寻常的原因。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.11925
K Ferdinande, T Lamiroy, A Hoorens, X Verhelst, H Degroote, S Raevens, H Van Vlierberghe, A Geerts
A 66-year-old male with a medical history of coronary artery disease presented with nonspecific symptoms of anorexia, lethargy and an increase in abdominal girth. He was diagnosed 3 months ago with chronic liver disease of undetermined aetiology. He did not smoke and was a social drinker till 4 months ago. He was taking tests showed progressive cholestatic liver enzymes (total bilirubin 1,09 mg/dL, AST 130 U/L, ALT 129 U/L, GGT 517 U/L and ALP 641 U/L) and a severe hypoalbuminemia. Laboratory workup made a metabolic, autoimmune, and viral aetiology of the suspected cirrhosis less probable. Urinalysis showed a rapidly progressive proteinuria in the nephrotic range accompanied by the presence of serum spike of monoclonal lambda light Furosemide, Aldactone, Pantoprazole, Acetylcysteine and Atorvastatin. He had no personal or familial history of liver diseases. Physical examination revealed a tender but distended abdomen and large ascites was present. The laboratory chain protein on electrophoresis with immunofixation. Doppler echocardiography revealed a hypertrophic cardiomyopathy based on diffuse left and right ventricular hypertrophy with relative apical sparing. A diagnostic paracentesis was undertaken and the results were consistent with portal hypertension (SAAG 1,6 g/ dL). Considering the concomitant presence of hypertrophic cardiomyopathy, nephrotic syndrome and a presentation of portal hypertension of undetermined aetiology in presence of a monoclonal IgG lambda light chain spike, a transjugular liver biopsy (figure 1 and 2) was performed with HVPG measurement consistent with significant portal hypertension (15 mmHg).
{"title":"An unusual cause of portal hypertension.","authors":"K Ferdinande, T Lamiroy, A Hoorens, X Verhelst, H Degroote, S Raevens, H Van Vlierberghe, A Geerts","doi":"10.51821/86.3.11925","DOIUrl":"10.51821/86.3.11925","url":null,"abstract":"A 66-year-old male with a medical history of coronary artery disease presented with nonspecific symptoms of anorexia, lethargy and an increase in abdominal girth. He was diagnosed 3 months ago with chronic liver disease of undetermined aetiology. He did not smoke and was a social drinker till 4 months ago. He was taking tests showed progressive cholestatic liver enzymes (total bilirubin 1,09 mg/dL, AST 130 U/L, ALT 129 U/L, GGT 517 U/L and ALP 641 U/L) and a severe hypoalbuminemia. Laboratory workup made a metabolic, autoimmune, and viral aetiology of the suspected cirrhosis less probable. Urinalysis showed a rapidly progressive proteinuria in the nephrotic range accompanied by the presence of serum spike of monoclonal lambda light Furosemide, Aldactone, Pantoprazole, Acetylcysteine and Atorvastatin. He had no personal or familial history of liver diseases. Physical examination revealed a tender but distended abdomen and large ascites was present. The laboratory chain protein on electrophoresis with immunofixation. Doppler echocardiography revealed a hypertrophic cardiomyopathy based on diffuse left and right ventricular hypertrophy with relative apical sparing. A diagnostic paracentesis was undertaken and the results were consistent with portal hypertension (SAAG 1,6 g/ dL). Considering the concomitant presence of hypertrophic cardiomyopathy, nephrotic syndrome and a presentation of portal hypertension of undetermined aetiology in presence of a monoclonal IgG lambda light chain spike, a transjugular liver biopsy (figure 1 and 2) was performed with HVPG measurement consistent with significant portal hypertension (15 mmHg).","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"509-510"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
EUS-guided transrectal drainage of pelvic abscesses: a retrospective analysis of 17 patients. EUS引导下经直肠引流治疗盆腔脓肿:17例患者的回顾性分析。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.12029
H Peeters, M Simoens, J Lenz

Background: Pelvic abscess is a common complication of abdominal surgery or intestinal or gynecological diseases. Over the last decades, endoscopic ultrasound (EUS)-guided drainage has emerged as a minimally invasive alternative to percutaneous or surgical treatment of pelvic abscesses.

Aim: To evaluate safety and efficacy of EUS-guided transrectal pelvic abscess drainage in a single center.

Methods: From February 2017 to April 2023, all data on patients who were treated for pelvic abscesses by EUS-guided drainage in a single center, were retrospectively analyzed.

Results: A total of 17 patients were treated for pelvic abscesses by EUS-guided drainage. The procedure was technically successful and uneventful in all 17 patients (100%). Etiology of the abscess was postsurgical (n=5, 29%), secondary to medical illness (n=10, 59%) or gastrointestinal perforation (n=2, 12%). The abscess was multilocular in 5 patients (29%), the mean largest diameter was 76 mm (range 40-146 mm). Drainage was performed using 2 double pigtail stents, and in 1 patient an additional 10 Fr drainage catheter was deployed. Two patients (12%) required a second endoscopic intervention. Treatment success, defined by complete abscess resolution on follow-up CT scan along with symptom relief, was 100%. There was no need for surgical intervention. The median post-procedural hospital stay was 5 days. No recurrence was reported within a median time of follow-up of 39 months.

Conclusion: EUS-guided transrectal drainage of pelvic abscesses using double pigtail stents is safe and highly effective. This case series contributes to the cumulative evidence that, in expert hands, EUS-guided drainage should be considered as first-line approach for treatment of pelvic abscesses.

背景:盆腔脓肿是腹部手术或肠道或妇科疾病的常见并发症。在过去的几十年里,内镜超声(EUS)引导引流已成为经皮或手术治疗盆腔脓肿的一种微创替代方法。目的:评价EUS引导下单中心经直肠盆腔脓肿引流术的安全性和有效性。方法:回顾性分析2017年2月至2023年4月在一个中心接受EUS引导引流治疗盆腔脓肿患者的所有数据。结果:共有17例患者接受了EUS引导下的盆腔脓肿引流治疗。该手术在技术上是成功的,所有17名患者(100%)都安然无恙。脓肿的病因为术后(n=5,29%),继发于内科疾病(n=10,59%)或胃肠道穿孔(n=2,12%)。脓肿为多房型5例(29%),平均最大直径为76mm(范围40-146mm)。使用2个双尾纤支架进行引流,1名患者使用额外的10Fr引流导管。两名患者(12%)需要第二次内镜介入治疗。治疗成功率为100%,其定义为在后续CT扫描中脓肿完全消退以及症状缓解。没有必要进行手术干预。术后平均住院时间为5天。中位随访时间39个月内无复发报告。结论:EUS引导下经直肠双尾纤支架引流治疗盆腔脓肿安全有效。该病例系列有助于累积证据,即在专家手中,EUS引导引流应被视为治疗盆腔脓肿的一线方法。
{"title":"EUS-guided transrectal drainage of pelvic abscesses: a retrospective analysis of 17 patients.","authors":"H Peeters,&nbsp;M Simoens,&nbsp;J Lenz","doi":"10.51821/86.3.12029","DOIUrl":"10.51821/86.3.12029","url":null,"abstract":"<p><strong>Background: </strong>Pelvic abscess is a common complication of abdominal surgery or intestinal or gynecological diseases. Over the last decades, endoscopic ultrasound (EUS)-guided drainage has emerged as a minimally invasive alternative to percutaneous or surgical treatment of pelvic abscesses.</p><p><strong>Aim: </strong>To evaluate safety and efficacy of EUS-guided transrectal pelvic abscess drainage in a single center.</p><p><strong>Methods: </strong>From February 2017 to April 2023, all data on patients who were treated for pelvic abscesses by EUS-guided drainage in a single center, were retrospectively analyzed.</p><p><strong>Results: </strong>A total of 17 patients were treated for pelvic abscesses by EUS-guided drainage. The procedure was technically successful and uneventful in all 17 patients (100%). Etiology of the abscess was postsurgical (n=5, 29%), secondary to medical illness (n=10, 59%) or gastrointestinal perforation (n=2, 12%). The abscess was multilocular in 5 patients (29%), the mean largest diameter was 76 mm (range 40-146 mm). Drainage was performed using 2 double pigtail stents, and in 1 patient an additional 10 Fr drainage catheter was deployed. Two patients (12%) required a second endoscopic intervention. Treatment success, defined by complete abscess resolution on follow-up CT scan along with symptom relief, was 100%. There was no need for surgical intervention. The median post-procedural hospital stay was 5 days. No recurrence was reported within a median time of follow-up of 39 months.</p><p><strong>Conclusion: </strong>EUS-guided transrectal drainage of pelvic abscesses using double pigtail stents is safe and highly effective. This case series contributes to the cumulative evidence that, in expert hands, EUS-guided drainage should be considered as first-line approach for treatment of pelvic abscesses.</p>","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"395-400"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Treatment of recurrent Clostridioides difficile infections with faecal microbiota transplantation: peri-procedural methods in a consecutive case series. 粪便微生物群移植治疗复发性艰难梭菌感染:连续病例系列的围手术期方法。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.11795
K Korpak, L Defourny, S Lali, M Delvallée, R Demeester, E Toussaint

Background: Faecal microbiota transplantation (FMT) has high efficacy against recurrent Clostridioides difficile infection (CDI). Despite the increasing use of this therapy, the delay between diagnosis and treatment is excessive. Furthermore, donor selection is an important and time-consuming process.

Methods: We reviewed patients who underwent FMT for recurrent CDI at the CHU Charleroi Hospital between 2015 and 2022. The general context, type of administration, adverse events, and donor selection were reported. FMT was conducted using gastroduodenoscopy, colonoscopy, and enema with either fresh or frozen material.

Results: Ten patients with multiple comorbidities were treated by FMT. Seven patients were cured after one procedure. One patient was successfully cured after a change to an unrelated donor, and preliminary efficacy was established.

Conclusions: FMT is an effective treatment that should be considered during the earlier phases of treatment. Stool donors should be thoroughly screened for infectious diseases and other criteria related to microbiota composition.

背景:粪便微生物群移植(FMT)对复发性艰难梭菌感染(CDI)具有很高的疗效。尽管这种疗法的使用越来越多,但诊断和治疗之间的延迟是过度的。此外,捐助者的选择是一个重要而耗时的过程。方法:我们回顾了2015年至2022年间在CHU Charleroi医院接受FMT治疗复发性CDI的患者。报告了一般情况、给药类型、不良事件和供体选择。FMT采用胃十二指肠镜、结肠镜和新鲜或冷冻材料灌肠进行。结果:10例合并多种疾病的患者均接受FMT治疗。7名患者在一次手术后治愈。一名患者在更换为无关供体后成功治愈,初步疗效已确定。结论:FMT是一种有效的治疗方法,应在治疗的早期阶段加以考虑。粪便捐献者应彻底筛查传染病和其他与微生物群组成有关的标准。
{"title":"Treatment of recurrent Clostridioides difficile infections with faecal microbiota transplantation: peri-procedural methods in a consecutive case series.","authors":"K Korpak,&nbsp;L Defourny,&nbsp;S Lali,&nbsp;M Delvallée,&nbsp;R Demeester,&nbsp;E Toussaint","doi":"10.51821/86.3.11795","DOIUrl":"10.51821/86.3.11795","url":null,"abstract":"<p><strong>Background: </strong>Faecal microbiota transplantation (FMT) has high efficacy against recurrent Clostridioides difficile infection (CDI). Despite the increasing use of this therapy, the delay between diagnosis and treatment is excessive. Furthermore, donor selection is an important and time-consuming process.</p><p><strong>Methods: </strong>We reviewed patients who underwent FMT for recurrent CDI at the CHU Charleroi Hospital between 2015 and 2022. The general context, type of administration, adverse events, and donor selection were reported. FMT was conducted using gastroduodenoscopy, colonoscopy, and enema with either fresh or frozen material.</p><p><strong>Results: </strong>Ten patients with multiple comorbidities were treated by FMT. Seven patients were cured after one procedure. One patient was successfully cured after a change to an unrelated donor, and preliminary efficacy was established.</p><p><strong>Conclusions: </strong>FMT is an effective treatment that should be considered during the earlier phases of treatment. Stool donors should be thoroughly screened for infectious diseases and other criteria related to microbiota composition.</p>","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"486-489"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
What do we know today about drug-induced microscopic colitis? A case of lymphocytic colitis on olmesartan. 我们今天对药物诱导的显微镜下结肠炎了解多少?奥美沙坦治疗淋巴细胞性结肠炎1例。
IF 1.5 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2023-07-01 DOI: 10.51821/86.3.11361
A Djembissi Fotso, M Arvanitakis, M Salame, J Gallez, A Lakis

Microscopic colitis is part of the differential diagnosis of chronic watery diarrhea. Colonoscopy discloses a normal looking mucosa, therefore its diagnosis is based on histology of colonic biopsies. Two main phenotypes are distinguished: collagenous colitis and lymphocytic colitis. A third entity, incomplete microscopic colitis or unspecified microscopic colitis has been reported in the literature. It affects preferentially women over 60 years of age and its association with certain drugs is increasingly established. In case of suspected drug-induced microscopic colitis, identification of the responsible drug is a key to management. After discontinuation of the suspected drug, the gold standard of treatment is budesonide both for induction and for maintenance in case of clinical relapse, as is often the case after discontinuation. Therapy with immunomodulators, biologics, or surgery is reserved for refractory forms of microscopic colitis after multidisciplinary consultation. Through the clinical case of colitis on olmesartan, we will review the latest recommendations on drug-induced microscopic colitis.

显微镜下结肠炎是鉴别诊断慢性水样腹泻的一部分。结肠镜检查显示粘膜外观正常,因此其诊断是基于结肠活检的组织学。有两种主要表型:胶原性结肠炎和淋巴细胞性结肠炎。第三种实体,不完全性显微镜下结肠炎或未指明的显微镜下结肠炎已在文献中报道。它优先影响60岁以上的女性,而且它与某些药物的联系越来越牢固。在疑似药物诱导的显微镜下结肠炎的情况下,确定责任药物是管理的关键。停用可疑药物后,治疗的金标准是布地奈德,用于诱导和在临床复发的情况下维持,停药后通常也是如此。免疫调节剂、生物制剂或手术治疗保留用于多学科会诊后的难治性显微镜下结肠炎。通过奥美沙坦治疗结肠炎的临床案例,我们将回顾药物诱导显微镜下结肠炎的最新建议。
{"title":"What do we know today about drug-induced microscopic colitis? A case of lymphocytic colitis on olmesartan.","authors":"A Djembissi Fotso,&nbsp;M Arvanitakis,&nbsp;M Salame,&nbsp;J Gallez,&nbsp;A Lakis","doi":"10.51821/86.3.11361","DOIUrl":"10.51821/86.3.11361","url":null,"abstract":"<p><p>Microscopic colitis is part of the differential diagnosis of chronic watery diarrhea. Colonoscopy discloses a normal looking mucosa, therefore its diagnosis is based on histology of colonic biopsies. Two main phenotypes are distinguished: collagenous colitis and lymphocytic colitis. A third entity, incomplete microscopic colitis or unspecified microscopic colitis has been reported in the literature. It affects preferentially women over 60 years of age and its association with certain drugs is increasingly established. In case of suspected drug-induced microscopic colitis, identification of the responsible drug is a key to management. After discontinuation of the suspected drug, the gold standard of treatment is budesonide both for induction and for maintenance in case of clinical relapse, as is often the case after discontinuation. Therapy with immunomodulators, biologics, or surgery is reserved for refractory forms of microscopic colitis after multidisciplinary consultation. Through the clinical case of colitis on olmesartan, we will review the latest recommendations on drug-induced microscopic colitis.</p>","PeriodicalId":7322,"journal":{"name":"Acta gastro-enterologica Belgica","volume":"86 3","pages":"474-480"},"PeriodicalIF":1.5,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41181706","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Acta gastro-enterologica Belgica
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1