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1.
Ann Surg ; 264(6): 1016-1021, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26756755

RESUMO

OBJECTIVE: This study aimed to establish the incidence of postesophagectomy columnar metaplasia and dysplasia, and the timescale over which it develops. It also aimed to assess if this epithelium is molecularly similar to sporadic Barrett esophagus, thereby confirming suitability as a research model. BACKGROUND: Metaplasia in the esophageal remnant after esophagectomy is well described, but incidence and the potential for dysplasia are uncertain, and the clinical relevance unclear. Although proposed as a model for Barrett esophagus, no large studies have examined the molecular phenotype of postesophagectomy metaplasia. METHODS: Patients underwent prospective endoscopic evaluation having previously undergone esophagectomy. The macroscopic appearance of the esophageal remnant was noted and biopsies taken. Specimens were stained using hematoxylin and eosin and by immunohistochemistry for cytokeratins 7 and 20, and Chromogranin A-proteins which have a well described expression pattern in sporadic Barrett esophagus. RESULTS: Of the 126 eligible patients, 45 (36%) had evidence of metaplasia. There were no cases of dysplasia. Nonintestinalized columnar epithelium occurred earlier than specialized intestinal metaplasia (median 4.8 vs 8.1 yr; P = 0.025). Thirty-seven samples underwent immunohistochemical analysis. A classic cytokeratin 7/20 staining pattern was present in 23 cases (62%), within the prevalence range reported for sporadic Barrett. CONCLUSIONS: Columnar metaplasia is common following esophagectomy, but the absence of dysplasia in this large cohort is reassuring. Presence of specialized intestinal metaplasia is associated with increased time from surgery, suggesting this represents later disease. Immunohistochemistry staining is similar to sporadic Barrett, suggesting that this group of patients represent an accurate human model for the development of Barrett.


Assuntos
Esôfago de Barrett/patologia , Esôfago de Barrett/cirurgia , Esofagectomia , Adulto , Idoso , Idoso de 80 Anos ou mais , Biópsia , Esofagoscopia , Feminino , Humanos , Imuno-Histoquímica , Incidência , Masculino , Metaplasia/patologia , Pessoa de Meia-Idade , Fenótipo , Prevalência , Estudos Prospectivos
2.
Dig Dis Sci ; 60(5): 1187-94, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25424203

RESUMO

BACKGROUND: Trefoil proteins are believed to have an important role in mucosal protection and repair in the gastrointestinal tract. They are well recognized in Barrett's esophagus and considered a potential biomarker for the condition. Metaplasia occurring in the esophageal remnant after esophagectomy is a human model for the early stages of development of Barrett's esophagus. AIMS: To assess expression of trefoil proteins in post-esophagectomy columnar epithelium and to use trefoils as a molecular tool to understand regenerative mucosa in the esophagus. METHODS: Patients with columnar metaplasia in the esophageal remnant were recruited from a large esophago-gastric cancer center. Trefoil factor expression was determined using immunohistochemical techniques. RESULTS: Samples were obtained from 37 patients. TFF1 and TFF2 were expressed by all samples in a similar pattern to that described in studies of sporadic Barrett's esophagus. TFF3 was less widely expressed and was significantly associated with time elapsed between surgery and endoscopy. Median time from surgery to endoscopy was 8.1 years for patients with TFF3 expression versus 3.4 years for those without (p = 0.004). CONCLUSIONS: Widespread expression of trefoils in this environment suggests that these proteins have an important role in development of Barrett's metaplasia. TFF3 expression may be absent in the early stages of metaplasia and may represent more established columnar epithelium. Biopsy samples from post-esophagectomy patients provide a valuable resource to study the early stages of Barrett's esophagus.


Assuntos
Esôfago de Barrett/metabolismo , Neoplasias Esofágicas/química , Esôfago/química , Peptídeos/análise , Lesões Pré-Cancerosas/química , Adulto , Idoso , Esôfago de Barrett/patologia , Esôfago de Barrett/cirurgia , Biomarcadores Tumorais/análise , Biópsia , Progressão da Doença , Neoplasias Esofágicas/patologia , Neoplasias Esofágicas/cirurgia , Esofagectomia , Esofagoscopia , Esôfago/patologia , Esôfago/cirurgia , Feminino , Humanos , Imuno-Histoquímica , Masculino , Metaplasia , Pessoa de Meia-Idade , Mucosa/química , Mucosa/patologia , Estadiamento de Neoplasias , Lesões Pré-Cancerosas/patologia , Lesões Pré-Cancerosas/cirurgia , Valor Preditivo dos Testes , Estudos Prospectivos , Estudos Retrospectivos , Fator Trefoil-1 , Fator Trefoil-2 , Fator Trefoil-3 , Proteínas Supressoras de Tumor/análise
4.
Ann Thorac Surg ; 89(2): 604-6, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-20103354

RESUMO

Barrett's esophagus results from the long-term effects of both acid and bile reflux. After subtotal esophagectomy and reconstruction with a gastric tube, many patients experience profound reflux. Development of Barrett's epithelium in the esophageal remnant has been reported. Here we report the case of a man who was diagnosed with adenocarcinoma in his esophageal remnant on a background of Barrett's change 52 years after undergoing one of the first esophageal resections for benign disease as a child.


Assuntos
Adenocarcinoma/cirurgia , Esôfago de Barrett/cirurgia , Neoplasias Esofágicas/cirurgia , Estenose Esofágica/cirurgia , Esofagite Péptica/cirurgia , Complicações Pós-Operatórias/cirurgia , Adenocarcinoma/patologia , Anastomose Cirúrgica , Esôfago de Barrett/patologia , Biópsia , Neoplasias Esofágicas/patologia , Esofagoscopia , Seguimentos , Humanos , Jejunostomia/métodos , Jejuno/transplante , Masculino , Microcirurgia , Pessoa de Meia-Idade , Pescoço/cirurgia , Estadiamento de Neoplasias , Complicações Pós-Operatórias/patologia , Disfunção Primária do Enxerto/cirurgia , Reoperação , Toracotomia/métodos
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