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European Surgery
Erschienen in:

01.10.2015 | Short Communication

Selected commentary to “Treatment of Barrett’s esophagus with a novel focal cryoablation device: a safety and feasibility study”

verfasst von: I. Kristo, MD, F. M. Riegler, MD, R. Asari, MD, E. Cosentini, MD, Univ.-Prof. Dr. S. F. Schoppmann, MD

Erschienen in: European Surgery | Ausgabe 5/2015

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Auszug

Barrett’s esophagus (BE) is caused by gastroesophageal reflux disease (GERD) and harbors an increased risk for esophageal cancer [1‐3]. Via a sequence involving low- (LGD) and high-grade dysplasia (HGD), esophageal adenocarcinoma may develop (annual cancer risk: 0.1–0.7 %) [4, 5]. Indefinite for dysplasia (ID) defines a condition where the presence or absence of dysplasia cannot be accurately assessed, due to inflammatory changes in the mucosa. Re-endoscopy and biopsy sampling is recommended after a 3–4 weeks course of double dose proton pump inhibitor (PPI) therapy p.o. (i.e. 2 × 40 mg PPI). Diagnosis of BE is established if biopsies obtained from endoscopically visible segments, tongues or islands of columnar lined esophagus (CLE) contain goblet cells ± LGD, HGD or cancer [6]. …
Vorheriger Artikel Retroperitoneal necrotizing fasciitis secondary to Fournier’s gangrene
Nächster Artikel Erratum to: 8th annual meeting of Chinese College of Surgeons and 19th annual meeting of the European Society of Surgery
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Metadaten
Titel
Selected commentary to “Treatment of Barrett’s esophagus with a novel focal cryoablation device: a safety and feasibility study”
verfasst von
I. Kristo, MD
F. M. Riegler, MD
R. Asari, MD
E. Cosentini, MD
Univ.-Prof. Dr. S. F. Schoppmann, MD
Publikationsdatum
01.10.2015
Verlag
Springer Vienna
Erschienen in
European Surgery / Ausgabe 5/2015
Print ISSN: 1682-8631
Elektronische ISSN: 1682-4016
DOI
https://doi.org/10.1007/s10353-015-0340-x

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