The endoscopic diagnosis and treatment for Mallory-Weiss syndrome.
- Author:
Geun Am SONG
1
;
Tae Oh KIM
;
Dae Hwan KANG
;
Mong CHO
;
Ung Suk YANG
;
Sang Moon BAE
;
Soo Hyung RYU
;
Jun hyup AN
;
Seong Hwun LEE
Author Information
1. Department of Internal Medicine, College of Medicine, Pusan National University, Pusan, Korea.
- Publication Type:Original Article
- Keywords:
Mallory-Weiss syndrome;
Endoscopic band ligation
- MeSH:
Alcohol Drinking;
Cardia;
Diagnosis*;
Endoscopy;
Esophageal and Gastric Varices;
Esophagogastric Junction;
Esophagus;
Follow-Up Studies;
Gastritis;
Hemorrhage;
Lacerations;
Ligation;
Mallory-Weiss Syndrome*;
Nausea;
Precipitating Factors;
Vomiting
- From:Korean Journal of Medicine
2000;58(5):542-547
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Mallory-Weiss syndrome is a laceration of gastroesophageal junction due to abruptly increased intraabdominal pressure. Bleeding from Mallory-Weiss tears stops spontaneously within 2-3 days without specific therapy in 80-90% of cases, but in some cases, aggressive treatment is required due to massive bleeding. METHODS: Among two hundreds and fifteen cases of upper gastrointestinal bleeding from January 1997 to January 1999, twenty three cases (10.7%) were diagnosed as Mallory-Weiss syndrome by endoscopy. We assessed the site, number, coexisting diseases, precipitating factors and bleeding lesion according to the time interval after the tears. After supportive care or specific therapy, we performed follow-up endoscopy to evaluate the healing of the lesions. RESULT: The mean age was 49.1 years and male:female ratio was 4.8:1. The most common precipitating factors were nausea, vomiting and alcohol drinking. In twenty cases, coexisting diseases such as gastritis and esophageal varix were detected. As for the number of tears, one tear was the most common (69.6%), while two tears were identified in five cases and three were in two cases. Thirteen cases of the Mallory-Weiss tears were located on the gastroesophageal junction, seven cases on the lower esophagus, one case on the cardia and two cases from lower esophagus to cardia. Eighteen cases were diagnosed by endoscopy within 24 hours after bleeding, of whom fourteen cases had active bleeding. Among four cases diagnosed after 24 hours, endoscopic finding revealed active bleeding in two cases and blood clots in the other two cases. We treated thirteen cases with supportive care, one case with hypertonic saline injection and nine cases who had active bleeding or deep and long tears with endoscopic band ligation. One or two weeks later, we performed follow-up endoscopy, and no bleeding was detected in all cases. CONCLUSION: We diagnosed twenty three cases of Mallory-Weiss syndrome by endoscopy and treated all cases with supportive care or endoscopic band ligation successfully.
