Boerhaave syndrome due to excessive alcohol consumption: two case reports

• Published in: International journal of emergency medicine Vol. 13; no. 1; p. 56
• Main Authors: Haba, Yuichiro, Yano, Shungo, Akizuki, Hikaru, Hashimoto, Takashi, Naito, Toshio, Hashiguchi, Naoyuki
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 30.11.2020; Springer Nature B.V; BMC
• Subjects: Alcohol use; Angiology; Boerhaave syndrome; Cardiology; Case Report; Case reports; Chest pain; Dyspnea; Emergency medical care; Emergency Medicine; Esophagus; Hematemesis; Internal Medicine; Mallory–Weiss syndrome; Medical diagnosis; Medicine; Medicine & Public Health; Ostomy; Pain; Pediatrics; Vomiting; Vomiting; Mallory–Weiss syndrome; Hematemesis; Chest pain; Boerhaave syndrome
• ISSN: 1865-1372; 1865-1380
• DOI: 10.1186/s12245-020-00318-5

Background Spontaneous esophageal rupture, or Boerhaave syndrome, is a fatal disorder caused by an elevated esophageal pressure owing to forceful vomiting. Patients with Boerhaave syndrome often present with chest pain, dyspnea, and shock. We report on two patients of Boerhaave syndrome with different severities that was triggered by excessive alcohol consumption and was diagnosed immediately in the emergency room. Case presentation The patient in case 1 complained of severe chest pain and nausea and vomited on arrival at the hospital. He was subsequently diagnosed with Boerhaave syndrome coupled with mediastinitis using computed tomography (CT) and esophagogram. An emergency operation was successfully performed, in which a 3-cm tear was found on the left posterior wall of the distal esophagus. The patient subsequently had anastomotic leakage but was discharged 41 days later. The patient in case 2 complained of severe chest pain, nausea, vomiting, and hematemesis on arrival. He was suggested of having Boerhaave syndrome without mediastinitis on CT. The symptoms gradually disappeared after conservative treatment. Upper gastrointestinal endoscopy performed on the ninth day revealed a scar on the left wall of the distal esophagus. The patient was discharged 11 days later. In addition to the varying severity between the cases, the patient in case 2 was initially considered to have Mallory–Weiss syndrome. Conclusion Owing to similar histories and symptoms, Boerhaave syndrome and Mallory–Weiss syndrome must be accurately distinguished by emergency clinicians. CT can be a useful modality to detect any severity of Boerhaave syndrome and also offers the possibility to distinguish Boerhaave syndrome from Mallory–Weiss syndrome.