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Inadequate steroid injection after esophageal ESD might cause mural necrosis
Background and study aims Locoregional triamcinolone acetonide (TAC) injection is increasingly used for prevention of stricture after extensive endoscopic submucosal dissection (ESD) for superficial esophageal neoplasia. However, the safety of intramural TAC injection has not been elucidated. The a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
© Georg Thieme Verlag KG
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336468/ https://www.ncbi.nlm.nih.gov/pubmed/30705941 http://dx.doi.org/10.1055/a-0781-2333 |
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author | Yamashita, Satoshi Kato, Motohiko Fujimoto, Ai Maehata, Tadateru Sasaki, Motoki Inoshita, Naoko Sato, Hiroki Suzuki, Kenji Yahagi, Naohisa |
author_facet | Yamashita, Satoshi Kato, Motohiko Fujimoto, Ai Maehata, Tadateru Sasaki, Motoki Inoshita, Naoko Sato, Hiroki Suzuki, Kenji Yahagi, Naohisa |
author_sort | Yamashita, Satoshi |
collection | PubMed |
description | Background and study aims Locoregional triamcinolone acetonide (TAC) injection is increasingly used for prevention of stricture after extensive endoscopic submucosal dissection (ESD) for superficial esophageal neoplasia. However, the safety of intramural TAC injection has not been elucidated. The aim of this study was to assess the clinical courses and histopathological changes after TAC injection into the muscle layer in a porcine model. Methods Three pigs were subjected to ESD under general anesthesia. Two artificial 30-mm lesions were created at the oral and anal ends of the esophagus in each pig. TAC was injected into the muscle layer of the artificial oral ulcers (TAC group) and saline was injected into the muscle layer of the artificial anal ulcers (control group). Endoscopic, macroscopic, and histopathological evaluations were performed. Results The artificial ulcers remained open at sacrifice on day 28 post-ESD in the three ulcers injected with TAC. Esophageal wall perforation and abscess spreading to the mediastinum were observed in two of the three ulcers in the TAC group. The abscesses involved the lungs, bronchi, and aortic adventitia. Severe inflammatory cell infiltration in the muscularis propria layer and significant muscularis propria degradation were observed in all three ulcers in the TAC group. Conclusions This study suggests that TAC may cause deep mural damage when it is injected into the muscularis propria. Care should be taken not to inject TAC into the muscle layer when it is used to prevent post-ESD stricture formation. |
format | Online Article Text |
id | pubmed-6336468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | © Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-63364682019-02-01 Inadequate steroid injection after esophageal ESD might cause mural necrosis Yamashita, Satoshi Kato, Motohiko Fujimoto, Ai Maehata, Tadateru Sasaki, Motoki Inoshita, Naoko Sato, Hiroki Suzuki, Kenji Yahagi, Naohisa Endosc Int Open Background and study aims Locoregional triamcinolone acetonide (TAC) injection is increasingly used for prevention of stricture after extensive endoscopic submucosal dissection (ESD) for superficial esophageal neoplasia. However, the safety of intramural TAC injection has not been elucidated. The aim of this study was to assess the clinical courses and histopathological changes after TAC injection into the muscle layer in a porcine model. Methods Three pigs were subjected to ESD under general anesthesia. Two artificial 30-mm lesions were created at the oral and anal ends of the esophagus in each pig. TAC was injected into the muscle layer of the artificial oral ulcers (TAC group) and saline was injected into the muscle layer of the artificial anal ulcers (control group). Endoscopic, macroscopic, and histopathological evaluations were performed. Results The artificial ulcers remained open at sacrifice on day 28 post-ESD in the three ulcers injected with TAC. Esophageal wall perforation and abscess spreading to the mediastinum were observed in two of the three ulcers in the TAC group. The abscesses involved the lungs, bronchi, and aortic adventitia. Severe inflammatory cell infiltration in the muscularis propria layer and significant muscularis propria degradation were observed in all three ulcers in the TAC group. Conclusions This study suggests that TAC may cause deep mural damage when it is injected into the muscularis propria. Care should be taken not to inject TAC into the muscle layer when it is used to prevent post-ESD stricture formation. © Georg Thieme Verlag KG 2019-02 2019-01-17 /pmc/articles/PMC6336468/ /pubmed/30705941 http://dx.doi.org/10.1055/a-0781-2333 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Yamashita, Satoshi Kato, Motohiko Fujimoto, Ai Maehata, Tadateru Sasaki, Motoki Inoshita, Naoko Sato, Hiroki Suzuki, Kenji Yahagi, Naohisa Inadequate steroid injection after esophageal ESD might cause mural necrosis |
title | Inadequate steroid injection after esophageal ESD might cause mural necrosis |
title_full | Inadequate steroid injection after esophageal ESD might cause mural necrosis |
title_fullStr | Inadequate steroid injection after esophageal ESD might cause mural necrosis |
title_full_unstemmed | Inadequate steroid injection after esophageal ESD might cause mural necrosis |
title_short | Inadequate steroid injection after esophageal ESD might cause mural necrosis |
title_sort | inadequate steroid injection after esophageal esd might cause mural necrosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336468/ https://www.ncbi.nlm.nih.gov/pubmed/30705941 http://dx.doi.org/10.1055/a-0781-2333 |
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