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Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis

Background and Aims. To explore the association of magnifying endoscopic (ME) findings with histopathology and relapse in ulcerative colitis (UC). Methods. Forty-six patients with UC underwent ME with narrow band imaging (NBI) and crystal violet staining and were followed for more than 12 months. ME...

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Autores principales: Isomoto, Hajime, Uehara, Ryohei, Hayashi, Tomayoshi, Shiota, Junya, Matsushima, Kayoko, Chen, Chun Chuan, Takeshima, Fuminao, Nakayama, Toshiyuki, Nakao, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807555/
https://www.ncbi.nlm.nih.gov/pubmed/24198828
http://dx.doi.org/10.1155/2013/671576
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author Isomoto, Hajime
Uehara, Ryohei
Hayashi, Tomayoshi
Shiota, Junya
Matsushima, Kayoko
Chen, Chun Chuan
Takeshima, Fuminao
Nakayama, Toshiyuki
Nakao, Kazuhiko
author_facet Isomoto, Hajime
Uehara, Ryohei
Hayashi, Tomayoshi
Shiota, Junya
Matsushima, Kayoko
Chen, Chun Chuan
Takeshima, Fuminao
Nakayama, Toshiyuki
Nakao, Kazuhiko
author_sort Isomoto, Hajime
collection PubMed
description Background and Aims. To explore the association of magnifying endoscopic (ME) findings with histopathology and relapse in ulcerative colitis (UC). Methods. Forty-six patients with UC underwent ME with narrow band imaging (NBI) and crystal violet staining and were followed for more than 12 months. ME findings with vital staining were classified into ME-A, regular arrangement of round to oval pits; ME-B, irregular arrangement with/without enlarged spaces between even pits; ME-C, irregular pits in size and shape with more irregular arrangement of pits; and ME-D, disrupted or disappeared pits. NBI-guided ME features of microvascular pattern (MVP) were divided into the MVP-regular and MVP-irregular type. Results. There were 5, 24, 10, and 7 cases of ME-A, ME-B, ME-C, and ME-D grade, respectively, while there were 21 and 25 of MVP-regular and MVP-irregular type, respectively. ME classifications were significantly associated with Matts endoscopic grade. ME classifications and MVP types were significantly associated with each pathognomonic microscopic feature of severe mucosal inflammation, crypt abscess, and goblet cell depletion. There were significant differences in the percentages of remission among ME classifications and between MVP types. Conclusion. ME findings can be predictive of relapse in UC and reliable for in vivo histopathological assessment.
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spelling pubmed-38075552013-11-06 Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis Isomoto, Hajime Uehara, Ryohei Hayashi, Tomayoshi Shiota, Junya Matsushima, Kayoko Chen, Chun Chuan Takeshima, Fuminao Nakayama, Toshiyuki Nakao, Kazuhiko Gastroenterol Res Pract Clinical Study Background and Aims. To explore the association of magnifying endoscopic (ME) findings with histopathology and relapse in ulcerative colitis (UC). Methods. Forty-six patients with UC underwent ME with narrow band imaging (NBI) and crystal violet staining and were followed for more than 12 months. ME findings with vital staining were classified into ME-A, regular arrangement of round to oval pits; ME-B, irregular arrangement with/without enlarged spaces between even pits; ME-C, irregular pits in size and shape with more irregular arrangement of pits; and ME-D, disrupted or disappeared pits. NBI-guided ME features of microvascular pattern (MVP) were divided into the MVP-regular and MVP-irregular type. Results. There were 5, 24, 10, and 7 cases of ME-A, ME-B, ME-C, and ME-D grade, respectively, while there were 21 and 25 of MVP-regular and MVP-irregular type, respectively. ME classifications were significantly associated with Matts endoscopic grade. ME classifications and MVP types were significantly associated with each pathognomonic microscopic feature of severe mucosal inflammation, crypt abscess, and goblet cell depletion. There were significant differences in the percentages of remission among ME classifications and between MVP types. Conclusion. ME findings can be predictive of relapse in UC and reliable for in vivo histopathological assessment. Hindawi Publishing Corporation 2013 2013-10-02 /pmc/articles/PMC3807555/ /pubmed/24198828 http://dx.doi.org/10.1155/2013/671576 Text en Copyright © 2013 Hajime Isomoto et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Isomoto, Hajime
Uehara, Ryohei
Hayashi, Tomayoshi
Shiota, Junya
Matsushima, Kayoko
Chen, Chun Chuan
Takeshima, Fuminao
Nakayama, Toshiyuki
Nakao, Kazuhiko
Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis
title Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis
title_full Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis
title_fullStr Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis
title_full_unstemmed Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis
title_short Magnifying Endoscopic Findings Can Predict Clinical Outcome during Long-Term Follow-Up of More Than 12 Months in Patients with Ulcerative Colitis
title_sort magnifying endoscopic findings can predict clinical outcome during long-term follow-up of more than 12 months in patients with ulcerative colitis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807555/
https://www.ncbi.nlm.nih.gov/pubmed/24198828
http://dx.doi.org/10.1155/2013/671576
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