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1.
Medicina (B Aires) ; 84(5): 997-1001, 2024.
Article in Spanish | MEDLINE | ID: mdl-39399943

ABSTRACT

Esophageal pathologies can exhibit extremely low incidence and prevalence rates. Therefore, it is essential to have multidisciplinary teams including surgeons specialized in esophageal pathology, with a high caseload, to ensure proper diagnosis and management. This manuscript presents a series of esophageal pathology cases with favorable outcomes and atypical resolution for non-specialized groups. However, failure to refer to specialists in a timely manner can result in missed diagnoses or poor quality of life for patients. These findings underscore the importance of having surgeons specialized in esophageal pathology and multidisciplinary teams to provide the best possible care for patients. Lusoria dysphagia (LD) is a condition caused by vascular compression of the esophagus, resulting from the most common embryological vascular abnormality of the aortic arch: the aberrant right subclavian artery (ARSA) or lusoria artery (LA). This variant occurs in 0.5 to 2.5% of individuals. Necrosis of the gastric tube following an esophagectomy is a rare complication with a high mortality rate. Esophageal replacement with coloplasty is the preferred technique for a second attempt at reconstruction. However, this remains a complex surgery with a high rate of complications.


Las enfermedades del esófago pueden presentar una incidencia y prevalencia extremadamente baja. Por lo tanto, es fundamental contar con equipos multidisciplinarios que incluyan cirujanos especializados en afecciones esofágicas, con un alto volumen de casos, para garantizar un diagnóstico y manejo adecuados. En este estudio, se analizan casos de enfermedad esofágica con resultados satisfactorios y una resolución atípica. La falta de derivación a especialistas a tiempo puede llevar a una ausencia de diagnóstico o una baja calidad de vida para los pacientes. Estos hallazgos subrayan la importancia de disponer de cirujanos especializados en esófago y equipos multidisciplinarios para asegurar la mejor atención posible para los pacientes.


Subject(s)
Deglutition Disorders , Humans , Deglutition Disorders/therapy , Deglutition Disorders/etiology , Male , Subclavian Artery/abnormalities , Patient Care Team , Middle Aged , Female , Esophagectomy/methods , Cardiovascular Abnormalities/therapy , Esophagus/abnormalities , Esophageal Diseases/therapy , Esophageal Diseases/diagnosis
2.
Ann Agric Environ Med ; 31(3): 450-454, 2024 Sep 25.
Article in English | MEDLINE | ID: mdl-39344738

ABSTRACT

Acute esophageal necrosis (AEN), known as black oesophagus or Gurvit's syndrome, is an extremely rare clinical syndrome. Patients usually present with life-threatening symptoms of upper gastrointestinal haemorrhage (70-90% of cases), as in this case report. Diagnosis of AEN is confirmed based on oesophagogastroduodenoscopy which reveals diffuse or patchy circumferential black necrotic oesophageal mucosa. The presented patient had some comorbidities, such as poorly controlled diabetes mellitus, secondary to chronic pancreatitis, hypertension, after cholecystectomy, addiction to alcohol and tobacco, and taking a small spoon of baking soda three times a day for a few months because of heartburn. Despite the poor prognosis of AEN, with mortality about 32-35%, most patients present with endoscopic improvement in short time - from 7 days to 1 month. Fortunately, the patient did not to have any complications in the course of AEN, and the treatment was effective.


Subject(s)
Necrosis , Humans , Male , Esophagus/pathology , Esophagus/surgery , Esophageal Diseases/pathology , Esophageal Diseases/etiology , Middle Aged
5.
BMC Gastroenterol ; 24(1): 310, 2024 Sep 14.
Article in English | MEDLINE | ID: mdl-39271994

ABSTRACT

BACKGROUND: Esophageal diseases (ED) are a kind of common diseases of upper digestive tract. Previous studies have proved that metabolic disorders are closely related to the occurrence and development of ED. However, there is a lack of evidence for causal relationships between metabolites and ED, as well as between metabolite ratios representing enzyme activities and ED. Herein, we explored the causality of genetically determined metabolites (GDMs) on ED through Mendelian Randomization (MR) study. METHODS: Two-sample Mendelian randomization analysis was used to assess the causal effects of genetically determined metabolites and metabolite ratios on ED. A genome-wide association analysis (GWAS) encompassing 850 individual metabolites along with 309 metabolite ratios served as the exposures. Meanwhile, the outcomes were defined by 10 types of ED phenotypes, including Congenital Malformations of Esophagus (CME), Esophageal Varices (EV), Esophageal Obstructions (EO), Esophageal Ulcers (EU), Esophageal Perforations (EP), Gastroesophageal Reflux Disease (GERD), Esophagitis, Barrett's Esophagus (BE), Benign Esophageal Tumors (BETs), and Malignant Esophageal Neoplasms (MENs). The standard inverse variance weighted (IVW) method was applied to estimate the causal relationship between exposure and outcome. Sensitivity analyses were carried out using multiple methods, including MR-Egger, Weighted Median, MR-PRESSO, Cochran's Q test, and leave-one-out analysis. P < 0.05 was conventionally considered statistically significant. After applying the Bonferroni correction for multiple testing, a threshold of P < 4.3E-05 (0.05/1159) was regarded as indicative of a statistically significant causal relationship. Furthermore, metabolic pathway analysis was performed using the web-based MetaboAnalyst 6.0 software. RESULTS: The findings revealed that initially, a total of 869 candidate causal association pairs ( P ivw < 0.05) were identified, involving 442 metabolites, 145 metabolite ratios and 10 types of ED. However, upon applying the Bonferroni correction for multiple testing, only 36 pairs remained significant, involving 28 metabolites (predominantly lipids and amino acids), 5 metabolite ratios and 6 types of ED. Sensitivity analyses and reverse MR were performed for these 36 causal association pairs, where the results showed that the pair of EV and 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (p-16:0/18:2) did not withstand the sensitivity tests, and Hexadecenedioate (C16:1-DC) was found to have a reverse causality with GERD. The final 34 robust causal pairs included 26 metabolites, 5 metabolite ratios and 5 types of ED. The involved 26 metabolites predominantly consisted of methylated nucleotides, glycine derivatives, sex hormones, phospholipids, bile acids, fatty acid dicarboxylic acid derivatives, and N-acetylated amino acids. Furthermore, through metabolic pathway analysis, we uncovered 8 significant pathways that played pivotal roles in five types of ED conditions. CONCLUSIONS: This study integrated genomics with metabolomics to assess causal relationships between ED and both metabolites and metabolite ratios, uncovering several key metabolic features in ED pathogenesis. These findings have potential as novel biomarkers for ED and provide insights into the disease's etiology and progression. However, further clinical and experimental validations are necessary.


Subject(s)
Esophageal Diseases , Genome-Wide Association Study , Mendelian Randomization Analysis , Humans , Esophageal Diseases/genetics , Esophageal Diseases/metabolism , Phenotype , Polymorphism, Single Nucleotide , Causality
6.
BMJ Case Rep ; 17(9)2024 Sep 03.
Article in English | MEDLINE | ID: mdl-39231567

ABSTRACT

This case report discusses a rare instance of polymicrobial pericarditis in a man in his early 60s with a history of substance abuse. The patient presented with chest pain and shortness of breath, later diagnosed as pericarditis caused by Streptococcus anginosus, S. intermedius and Candida glabrata, likely originating from a large adjacent oesophageal ulcer. The condition led to critical illness, requiring pericardiocentesis, antibiotic and antifungal therapy. Despite initial improvement, the patient experienced recurrence and ultimately underwent pericardectomy. The article emphasises the rarity and severity of polymicrobial pericarditis, often associated with high mortality. It underscores the importance of prompt recognition, broad-spectrum antibiotics and source control, particularly when the gastrointestinal tract is implicated. The case highlights the challenges in managing such cases and the potential need for surgical intervention for optimal outcomes.


Subject(s)
Candida glabrata , Candidiasis , Esophageal Diseases , Pericarditis , Ulcer , Humans , Male , Pericarditis/microbiology , Pericarditis/diagnosis , Candidiasis/complications , Candidiasis/diagnosis , Candidiasis/microbiology , Candidiasis/drug therapy , Ulcer/microbiology , Candida glabrata/isolation & purification , Esophageal Diseases/microbiology , Streptococcus anginosus/isolation & purification , Anti-Bacterial Agents/therapeutic use , Middle Aged , Streptococcus intermedius/isolation & purification , Streptococcal Infections/complications , Streptococcal Infections/microbiology , Streptococcal Infections/diagnosis , Streptococcal Infections/drug therapy , Antifungal Agents/therapeutic use , Bacterial Translocation , Coinfection , Pericardiocentesis , Pericardiectomy
8.
Magy Onkol ; 68(3): 215-220, 2024 Sep 19.
Article in Hungarian | MEDLINE | ID: mdl-39299687

ABSTRACT

The introduction of robot-assisted minimally invasive esophageal surgery (RAMIE) represents a significant advancement in minimally invasive surgery. The robot system typically includes a high-resolution 3D camera and specially maneuverable instruments that are controlled by the surgeon from a console. By reducing the trauma caused by the intervention, this method allows for faster recovery compared to traditional open surgeries. Furthermore, the increased range of motion provided by the robot instruments enables more precise manipulations in the area of the esophagus and surrounding tissues, thereby improving the effectiveness of tumor resections and reconstructions. The results of clinical trials are promising: there is a decrease in postoperative pain, a lower risk of complications, and a shorter hospital stay, while the oncological outcomes are at least equivalent to open surgeries. As technology advances, robot-assisted esophageal surgery is expected to spread more widely, providing better patient care and surgical outcomes for both benign and malignant esophageal diseases.


Subject(s)
Esophageal Neoplasms , Esophagectomy , Robotic Surgical Procedures , Humans , Esophageal Neoplasms/surgery , Esophagectomy/methods , Esophagectomy/instrumentation , Robotic Surgical Procedures/methods , Robotic Surgical Procedures/instrumentation , Treatment Outcome , Length of Stay , Esophageal Diseases/surgery , Robotics/instrumentation , Robotics/methods , Minimally Invasive Surgical Procedures/methods , Minimally Invasive Surgical Procedures/instrumentation , Pain, Postoperative/etiology , Pain, Postoperative/prevention & control
9.
Tidsskr Nor Laegeforen ; 144(11)2024 Sep 24.
Article in Norwegian | MEDLINE | ID: mdl-39319767

ABSTRACT

Background: Spontaneous rupture of the oesophagus is a potentially fatal condition. Symptoms can vary and diagnosis can be challenging. Case presentation: A woman in her seventies presented to the emergency department with sudden-onset epigastric pain after a meal. A computed tomography (CT) showed signs of oesophageal rupture. Upper gastrointestinal endoscopy revealed an oesophageal rupture, and a stent was placed. The patient developed fever, dyspnoea and hypotension after the procedure. Additional CT revealed increasing pleural effusion, pneumomediastinum and loculaments of air in the peritoneum, and a mediastinal abscess. Laparoscopy with lavage and debridement was performed. A catheter was placed in the abscess and a chest tube in her right hemithorax. The stent was removed after 27 days. Further investigation revealed eosinophil oesophagitis as the likely cause of her oesophageal rupture. Interpretation: This case highlights the importance of early diagnosis and proper treatment of spontaneous oesophageal rupture. Treatment depends on the cause of the rupture and severity of the patient's condition.


Subject(s)
Tomography, X-Ray Computed , Humans , Female , Rupture, Spontaneous , Aged , Stents , Eosinophilic Esophagitis/diagnosis , Eosinophilic Esophagitis/complications , Eosinophilic Esophagitis/therapy , Esophageal Diseases/diagnosis , Esophageal Diseases/etiology , Esophageal Diseases/diagnostic imaging , Esophageal Perforation/etiology , Esophageal Perforation/diagnosis , Esophageal Perforation/diagnostic imaging , Esophageal Perforation/surgery
10.
J Affect Disord ; 366: 189-195, 2024 Dec 01.
Article in English | MEDLINE | ID: mdl-39187201

ABSTRACT

BACKGROUND: Previous studies have suggested a potential association between irritability and the risk of various diseases. However, establishing a causal relationship has remained a significant challenge. To address this issue, we employed Mendelian randomization (MR), a sophisticated approach that leverages genotype data to emulate the conditions of randomized controlled trials. This method enables us to investigate the potential causal link between irritability and the susceptibility to esophageal diseases. METHODS: We conducted an extensive multivariable MR analysis using summary-level data from genome-wide association studies (GWAS) encompassing various esophageal diseases, including gastroesophageal reflux disease (GERD), esophageal cancer (EC), and Barrett's esophagus. Both univariable and multivariable MR analyses were performed to elucidate and confirm the causal association between genetically predicted irritability and the incidence of esophageal diseases. RESULTS: Based on our primary causal effects model utilizing MR analyses with the inverse-variance weighted (IVW) method, genetically predicted irritability was identified as a risk factor for GERD (OR = 2.413; 95 % CI: 1.678-3.470; P = 2.03E-06) and Barrett's esophagus (OR = 2.306; 95 % CI: 1.042-5.101; P = 0.039). However, irritability was not found to be associated with the risk of EC, even after adjusting for BMI, smoking initiation, and alcohol consumption. CONCLUSION: The multivariable MR analysis performed in this study demonstrated a causal relationship between irritability and esophageal diseases. It is imperative to acknowledge the need for further large-scale prospective studies to validate these findings.


Subject(s)
Barrett Esophagus , Esophageal Neoplasms , Gastroesophageal Reflux , Genome-Wide Association Study , Irritable Mood , Mendelian Randomization Analysis , Humans , Barrett Esophagus/genetics , Gastroesophageal Reflux/genetics , Gastroesophageal Reflux/epidemiology , Esophageal Neoplasms/genetics , Esophageal Neoplasms/epidemiology , Risk Factors , Esophageal Diseases/genetics , Polymorphism, Single Nucleotide , Genetic Predisposition to Disease/genetics
11.
J Investig Med High Impact Case Rep ; 12: 23247096241269864, 2024.
Article in English | MEDLINE | ID: mdl-39107990

ABSTRACT

Acute esophageal necrosis (AEN), also known as Gurvits syndrome, is a rare and potentially life-threatening condition characterized by necrosis of the esophageal mucosa. Acute esophageal necrosis is often associated with critical conditions, such as myocardial infarction, diabetic ketoacidosis (DKA), coronavirus disease 2019 (COVID-19) infection, or post-surgical complications. Patients typically present with nausea, hematemesis, acute dysphagia, and melena. Given its high mortality rate, prompt detection with upper endoscopy and early initiation of treatment are crucial. Most cases of Gurvits syndrome are managed conservatively using intravenous fluids, proton pump inhibitors, and antibiotics. Herein, we present a case series of AEN in the setting of DKA. Both patients received supportive care and were discharged in a stable condition.


Subject(s)
Diabetic Ketoacidosis , Necrosis , Humans , Diabetic Ketoacidosis/complications , Male , Middle Aged , Female , Esophagus/pathology , Esophageal Diseases/pathology , COVID-19/complications , Adult , Acute Disease
13.
Turk J Gastroenterol ; 35(7): 587-588, 2024 Jul.
Article in English | MEDLINE | ID: mdl-39128110

ABSTRACT

Cite this article as: Zong Z, Xu J, Zhang H, Xu H, Tang X, Shi L. A small "tent" in the esophagus. Turk J Gastroenterol. 2024;35(7): 587-588.


Subject(s)
Esophagus , Humans , Male , Esophageal Diseases , Female
14.
Aliment Pharmacol Ther ; 60(6): 715-726, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39082463

ABSTRACT

BACKGROUND: Oesophageal disorders and chronic liver disease are common worldwide and significantly impact quality of life. The intricate link between these conditions, including how oesophageal disorders like GERD, Barrett's oesophagus and oesophageal cancer affect and are affected by chronic liver disease, remains poorly understood. AIMS: To review the relationship between oesophageal disorders and chronic liver disease, evaluating epidemiology, pathophysiology and therapeutic factors. METHODS: We reviewed the literature on the relationship between oesophageal disorders and chronic liver disease, including cirrhosis, using the PubMed database RESULTS: Oesophageal disorders such as gastroesophageal reflux disease, Barrett's oesophagus, oesophageal cancer, oesophageal motor disorders and oesophageal candidiasis are prevalent among individuals with cirrhosis, exacerbating the burden of liver disease. These diseases have a multifaceted symptomatology and pathogenic basis, posing a significant challenge in cirrhotic patients that necessitates careful diagnosis and management. Additionally, therapies frequently used for these diseases, such as proton pump inhibitors, require careful consideration in cirrhotic patients due to potential adverse effects and altered pharmacokinetics. Managing oesophageal disorders in cirrhotic patients requires a cautious approach due to possible interactions with medications and the risk of adverse effects. Furthermore, symptoms associated with these conditions are often exacerbated by common interventions in patients with cirrhosis, such as band ligation for oesophageal varices. CONCLUSIONS: Oesophageal disorders are common in cirrhosis and increase the disease burden. These conditions require careful management due to complex symptoms and treatment risks. Proton pump inhibitors and other therapies must be used cautiously, as cirrhosis interventions can worsen symptoms.


Subject(s)
Esophageal Diseases , Liver Diseases , Humans , Esophageal Diseases/physiopathology , Esophageal Diseases/etiology , Esophageal Diseases/complications , Liver Diseases/complications , Liver Diseases/physiopathology , Chronic Disease , Liver Cirrhosis/complications , Liver Cirrhosis/physiopathology , Quality of Life , Gastroesophageal Reflux/complications , Gastroesophageal Reflux/physiopathology , Proton Pump Inhibitors/therapeutic use
15.
Dig Liver Dis ; 56(10): 1675-1682, 2024 Oct.
Article in English | MEDLINE | ID: mdl-38851975

ABSTRACT

BACKGROUD: The use of neuromodulators is prevalent in various functional gastrointestinal disease. However, data concerning the outcomes of these treatments in functional esophageal disorders (FED) remains limited and inadequate. AIMS: The aim of the present study is to examine the efficacy of central neuromodulators in FED. METHODS: We searched PubMed, EMBASE, and the Cochrane library databases from inception to April 2023. Randomized controlled trials that compared the effects of neuromodulators and placebos on FED are included. Primary outcome is the symptom improvement, and Rome IV criteria is used to assess eligible studies. RESULTS: Eleven randomized controlled studies (three for functional chest pain, four for reflux hypersensitivity/functional heartburn, three for globus, and one for functional dysphagia) were included in the final analysis. Neuromodulators reduced chest pain by 52%-71% in patients with functional chest pain, and alleviated symptom by 46%-75% in patients with globus (n = 3, Odds ratio 6.30, 95% confidence interval 4.17-9.50). However, the results were inconsistent for reflux hypersensitivity and functional heartburn. There was a lack of convincing evidence to support the use of neuromodulators for functional dysphagia. The use of neuromodulators did not have a significant impact on the quality of life. CONCLUSIONS: Functional chest pain and globus may potentially benefit from the use of neuromodulators, but their effectiveness for functional dysphagia, functional heartburn and reflux hypersensitivity remains controversial. More controlled trials are needed to confirm the therapeutic effects on these conditions.


Subject(s)
Chest Pain , Deglutition Disorders , Heartburn , Neurotransmitter Agents , Randomized Controlled Trials as Topic , Humans , Neurotransmitter Agents/therapeutic use , Chest Pain/drug therapy , Chest Pain/etiology , Heartburn/drug therapy , Heartburn/etiology , Deglutition Disorders/drug therapy , Esophageal Diseases/drug therapy , Gastroesophageal Reflux/drug therapy , Treatment Outcome
16.
J Gastroenterol Hepatol ; 39(10): 2097-2104, 2024 Oct.
Article in English | MEDLINE | ID: mdl-38860301

ABSTRACT

BACKGROUND AND AIM: Patients with proton-pump-inhibitor (PPI)-unresponsive reflux symptoms, often caused by functional esophageal disorders (FED), are frequently encountered in clinical practice. We aimed to investigate the prevalence of FED and its associated clinical characteristics in patients with PPI-unresponsive reflux symptoms. METHODS: We retrospectively identified patients who were evaluated for persistent typical reflux symptoms, despite ≥8 weeks of PPI treatment, at the National Taiwan University Hospital from 2014 to 2023. All patients underwent a comprehensive evaluation comprising validated gastroesophageal reflux disease (GERD) symptom questionnaires, 5-item Brief Symptom Rating Scale (BSRS-5), Pittsburgh Sleep Quality Index (PSQI), esophagogastroduodenoscopy, high-resolution impedance manometry, and 24-h impedance-pH monitoring off PPI therapy. Diagnosis of FED and non-erosive reflux disease (NERD) was based on the Rome IV criteria. RESULTS: We analyzed 190 patients [46.8% male, median age 52 (interquartile range, 42-61) years], of whom 32 (16.8%) had NERD and 158 (83.2%) had FED (57.9% with functional heartburn and 25.3% with reflux hypersensitivity). Patients with FED had a lower body mass index than those with NERD and a higher prevalence of psychological comorbidities and poor sleep quality than healthy volunteers. The severity of reflux symptoms among FED patients was significantly associated with the severity of psychological comorbidities and sleep quality. CONCLUSIONS: A notably high prevalence (83.2%) of FED was observed among patients experiencing PPI-unresponsive reflux symptoms. Patients with FED had a higher level of psychological distress and diminished sleep quality, both of which were associated with reflux symptom severity.


Subject(s)
Gastroesophageal Reflux , Proton Pump Inhibitors , Humans , Male , Proton Pump Inhibitors/therapeutic use , Female , Middle Aged , Prevalence , Adult , Retrospective Studies , Gastroesophageal Reflux/epidemiology , Gastroesophageal Reflux/drug therapy , Gastroesophageal Reflux/diagnosis , Surveys and Questionnaires , Esophageal Diseases/epidemiology , Esophageal Diseases/etiology , Esophageal Diseases/diagnosis , Taiwan/epidemiology , Esophageal pH Monitoring , Manometry , Sleep Quality , Endoscopy, Digestive System , Treatment Failure
17.
Z Gastroenterol ; 62(9): 1384-1388, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38917831

ABSTRACT

As of now, there exists no established therapy for ELP. Retinoids, which are standard in treating cutaneous LP, do not exhibit positive effects in ELP. While topical glucocorticosteroids often yield favorable responses in esophageal inflammation, some cases prove recalcitrant or refractory. In such instances, various immunosuppressive therapies have been attempted with variable success.This report details a severe case of ELP that showed resistance to prednisolone, acitretin, alitretinoin, adalimumab, tacrolimus, hydroxychloroquine plus mycophenolate mofetil, and cyclophosphamide. The initiation of the JAK inhibitor tofacitinib induced an impressive clinical, endoscopic, and histological remission. This positive response to a JAK inhibitor is discussed in the context of our evolving understanding of the immune-mediated pathogenesis of this disease.


Subject(s)
Lichen Planus , Piperidines , Pyrimidines , Pyrroles , Humans , Piperidines/therapeutic use , Piperidines/adverse effects , Pyrimidines/therapeutic use , Pyrimidines/adverse effects , Lichen Planus/drug therapy , Lichen Planus/chemically induced , Lichen Planus/pathology , Treatment Outcome , Pyrroles/therapeutic use , Pyrroles/adverse effects , Esophageal Diseases/drug therapy , Esophageal Diseases/chemically induced , Esophageal Diseases/pathology , Remission Induction , Middle Aged , Male , Female
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