Magnifying Endoscopy with Narrow Band Imaging of Early Gastric Cancer: Correlation with Histopathology and Mucin Phenotype.
- Author:
Kyung Sun OK
1
;
Gwang Ha KIM
;
Do Youn PARK
;
Hyun Jeong LEE
;
Hye Kyung JEON
;
Dong Hoon BAEK
;
Bong Eun LEE
;
Geun Am SONG
Author Information
- Publication Type:Original Article
- Keywords: Magnifying endoscopy; Narrow band imaging; Stomach neoplasms; Mucins
- MeSH: Endoscopy*; Gastrointestinal Tract; Humans; Immunohistochemistry; Mucins*; Narrow Band Imaging*; Phenotype*; Prospective Studies; Stomach Neoplasms*
- From:Gut and Liver 2016;10(4):532-541
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND/AIMS: Magnifying endoscopy with narrow band imaging (ME-NBI) is a useful modality for the detailed visualization of microsurface (MS) and microvascular (MV) structures in the gastrointestinal tract. This study aimed to determine whether the MS and MV patterns in ME-NBI differ according to the histologic type, invasion depth, and mucin phenotype of early gastric cancers (EGCs). METHODS: The MS and MV patterns of 160 lesions in 160 patients with EGC who underwent ME-NBI before endoscopic or surgical resection were prospectively collected and analyzed. EGCs were categorized as either differentiated or undifferentiated and as either mucosal or submucosal, and their mucin phenotypes were determined via immunohistochemistry of the tumor specimens. RESULTS: Differentiated tumors mainly displayed an oval and/or tubular MS pattern and a fine network or loop MV pattern, whereas undifferentiated tumors mainly displayed an absent MS pattern and a corkscrew MV pattern. The destructive MS pattern was associated with submucosal invasion, and this association was more prominent in the differentiated tumors than in the undifferentiated tumors. MUC5AC expression was increased in lesions with either a papillary or absent MS pattern and a corkscrew MV pattern, whereas MUC6 expression was increased in lesions with a papillary MS pattern and a loop MV pattern. CD10 expression was more frequent in lesions with a fine network MV pattern. CONCLUSIONS: ME-NBI can be useful for predicting the histopathology and mucin phenotype of EGCs.
