Revista de Gastroenterología de México (English Edition) (Jan 2014)

Boerhaave's syndrome: A review of our experience over the last 16 years

  • L. Granel-Villach,
  • C. Fortea-Sanchis,
  • D. Martínez-Ramos,
  • G.A. Paiva-Coronel,
  • R. Queralt-Martín,
  • A. Villarín-Rodríguez,
  • J.L. Salvador-Sanchis

DOI
https://doi.org/10.1016/j.rgmxen.2013.11.001
Journal volume & issue
Vol. 79, no. 1
pp. 67 – 70

Abstract

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Objective: Report our experience in the diagnosis and treatment of Boerhaave syndrome by retrospective study from 1997 to 2013. Patients and methods: A retrospective study was conducted covering the time frame of 1997 to 2013. Results: There were a total of 5 men (71%) and 2 women (29%) and the mean age was 54 years (range: 33-80 years). Diagnosis was made through computed tomography scan in 5 cases (71%) and esophagogram in 2 cases (19%). Six patients (86%) had emergency surgery, whereas one case (14%) was managed conservatively. The surgical technique employed was primary suture and repair in 4 patients (67%) and esophageal resection and subsequent cervical esophagostomy in 2 patients (33%). Conclusions: Boerhaave's syndrome is a clinically rare entity with an elevated mortality rate. Therefore, a high degree of suspicion is necessary for making the diagnosis and providing early treatment that can result in improved outcome.

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