Published online Jun 16, 2022. doi: 10.12998/wjcc.v10.i17.5620
Peer-review started: December 8, 2021
First decision: March 11, 2022
Revised: March 17, 2022
Accepted: April 9, 2022
Article in press: April 9, 2022
Published online: June 16, 2022
Processing time: 182 Days and 14.7 Hours
There is significant heterogeneity between gastroesophageal varices (GOV2) and isolated gastric varices (IGV1). The data on the difference between GOV2 and IGV1 are limited.
The Sarin classification does not truly describe the heterogeneity in the etiology and vascular alternation. Thus, studies should be performed to determine the etiology, clinical profiles, and imaging signs in patients with GOV2 and IGV1.
The Sarin classification does not truly describe the heterogeneity in the etiology To obtain a better understanding of fundic varices (GOV2 and IGV1), a large sample of patients (119 patients with GOV2, 133 patients with IGV1) was enrolled, and then the etiology, clinical profiles, endoscopic findings, imaging signs, and portosystemic collateral veins in patients with fundic varices were investigated in our study. The data in our study are helpful in making therapeutic decisions.
The authors retrospectively collected the medical records of 252 patients with gastric fundal varices, and analyzed computed tomography images.
Significant differences in the etiology, blood routine examination, liver function, the incidence of peptic ulcer and the morbidity of portal hypertensive gastropathy were found between GOV2 and IGV1. Typical radiological signs of liver cirrhosis were more commonly observed in patients with GOV2 compared with IGV1. Spleno-gastroomental-superior mesenteric shunt was a major collateral vessel of IGV1 patients caused by the obstruction of the splenic vein. Gastro-renal shunt or gastrocaval shunt occurred in GOV2 patients with small size of esophageal varices and IGV1 patients caused by liver cirrhosis
These findings highlight the differences in the etiology, clinical profiles, endoscopic findings, imaging signs, portosystemic collaterals between patients with GOV2 and patients with IGV1. Knowledge of the etiology and portosystemic collaterals in our study is helpful in making therapeutic decisions.
A multicenter study should be performed to determine the differences in the etiology, clinical profiles, endoscopic findings, imaging signs, portosystemic collaterals between patients with GOV2 and patients with IGV1. A prospective RCT study should be performed to determine therapeutic interventions for patients with GOV2 or IGV1.