Published online Jan 28, 2015. doi: 10.3748/wjg.v21.i4.1268
Peer-review started: May 4, 2014
First decision: June 27, 2014
Revised: July 22, 2014
Accepted: September 18, 2014
Article in press: September 19, 2014
Published online: January 28, 2015
Processing time: 272 Days and 0.9 Hours
AIM: To determine whether the endoscopic findings of depressed-type early gastric cancers (EGCs) could precisely predict the histological type.
METHODS: Ninety depressed-type EGCs in 72 patients were macroscopically and histologically identified. We evaluated the microvascular (MV) and mucosal surface (MS) patterns of depressed-type EGCs using magnifying endoscopy (ME) with narrow-band imaging (NBI) (NBI-ME) and ME enhanced by 1.5% acetic acid, respectively. First, depressed-type EGCs were classified according to MV pattern by NBI-ME. Subsequently, EGCs unclassified by MV pattern were classified according to MS pattern by enhanced ME (EME) images obtained from the same angle.
RESULTS: We classified the depressed-type EGCs into the following 2 MV patterns using NBI-ME: a fine-network pattern that indicated differentiated adenocarcinoma (25/25, 100%) and a corkscrew pattern that likely indicated undifferentiated adenocarcinoma (18/23, 78.3%). However, 42 of the 90 (46.7%) lesions could not be classified into MV patterns by NBI-ME. These unclassified lesions were then evaluated for MS patterns using EME, which classified 33 (81.0%) lesions as MS patterns, diagnosed as differentiated adenocarcinoma. As a result, 76 of the 90 (84.4%) lesions were matched with histological diagnoses using a combination of NBI-ME and EME.
CONCLUSION: A combination of NBI-ME and EME was useful in predicting the histological type of depressed-type EGC.
Core tip: Prediction of the histological diagnosis of early gastric cancer (EGC) using endoscopy is important for determining the appropriate therapeutic approach. In the present study, we combined magnifying endoscopy (ME) with narrow-band imaging (NBI) and enhanced ME (EME) to determine the associations between microvascular (MV) and mucosal surface (MS) patterns of depressed-type EGCs and the histological type. Indeed, 82 of the 90 lesions (91.1%) were classified according to MV or MS pattern, and 76 of the 90 lesions (84.4%) were diagnosed according to histological type. Therefore, our study suggested that the NBI-EME combination was useful for diagnosing the histological type in depressed-type EGC.