Back to Search Start Over

Characteristic endoscopic findings of gastric adenocarcinoma of fundic-gland mucosa type

Authors :
Kenshi Yao
Kentaro Imamura
Toshiharu Ueki
Satoshi Nimura
Takao Kanemitsu
Hiroshi Tanabe
Yoichiro Ono
Akinori Iwashita
Masaki Miyaoka
Source :
Gastric Cancer. 24:1307-1319
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

Gastric adenocarcinoma of fundic-gland type (GA-FG) was first proposed as a new entity of gastric adenocarcinoma in 2010. Subsequently, gastric adenocarcinoma of fundic-gland mucosa type (GA-FGM) was reported as a subtype of gastric adenocarcinoma. This study aimed to investigate the endoscopic findings of GA-FGM and to evaluate the differences between GA-FGM and GA-FG. This was a single-center retrospective study. Participants were selected from patients with gastric cancer treated at Fukuoka University Chikushi Hospital, between September 2007 and May 2020. Patients histologically diagnosed with GA-FGM or GA-FG were enrolled, and endoscopic findings were analyzed in detail. A total of 12 GA-FGM lesions (12 patients) and 14 GA-FG lesions (13 patients) were analyzed. The two lesion types showed similar features: most lesions were of elevated type, located in the upper stomach, and developed in the stomach without Helicobacter pylori infection. On conventional endoscopy using the dye-spraying method, well-demarcated fine granular areas were observed in 7 GA-FGM lesions (58%) but not in any GA-FG lesions, with a significant difference between the two groups (P = 0.001). Magnifying endoscopy with narrow-band imaging (NBI) showed that 11 GA-FGM lesions (92%) met the diagnostic criteria for cancer according to the vessel plus surface classification system, whereas none of the GA-FG lesions met the same criteria (0%, 0/14) (P = 0.001). Our results suggest that magnifying endoscopy with NBI is a potentially useful method for the diagnosis of GA-FGM.

Details

ISSN :
14363305 and 14363291
Volume :
24
Database :
OpenAIRE
Journal :
Gastric Cancer
Accession number :
edsair.doi.dedup.....5cf1420f4023514c63208b11dde1ad24