'Boerhaave syndrome' (also called 'Boerhaave's syndrome') is rupture of the
esophagus. It is generally caused by excessive
vomiting in
eating disorders such as
bulimia although it may rarely occur in extremely forceful
coughing or other situations. It can cause
pneumomediastinum and/or
mediastinitis (air or inflammation of the
mediastinum) and
sepsis. This condition was first documented by the 18th-century physician
Herman Boerhaave, after whom it is named.
Symptoms
It typically occurs after forceful
vomiting. Boerhaave syndrome is a transmural perforation (full-thickness; a 'hole') of the
esophagus, distinct from
Mallory-Weiss syndrome, a nontransmural esophageal 'tear' also associated with vomiting. Because it is generally associated with vomiting, Boerhaave syndrome usually is not truly spontaneous. However, the term is useful for distinguishing it from
iatrogenic perforation, which accounts for 85-90% of cases of esophageal rupture, typically as a complication of an
endoscopic procedure, feeding tube, or unrelated
surgery. Boerhaave syndrome is often seen as a complication of Bulimia.
The classic Meckler's triad of symptoms includes vomiting, lower chest pain, and cervical subcutaneous emphysema following overindulgence in
food or
alcohol, but is observed in only half of the cases. The most common chest
radiograph findings in spontaneous esophageal rupture (SER) are
pleural effusion (91%) and
pneumothorax (80%). The initial sign on a plain film may be
pneumomediastinum or subcutaneous emphysema. Up to 12% of patients with SER may have a normal chest radiograph. Contrast-enhanced esophageal radiography is diagnostic in 75% to 85% of cases.
[1]
Pathophysiology
Esophageal rupture in Boerhaave syndrome is thought to be the result of a sudden rise in internal esophageal pressure produced during vomiting, as a result of neuromuscular incoordination causing failure of the cricopharyngeus muscle (a
sphincter within the esophagus) to relax. The syndrome is commonly associated with the consumption of excessive food and/or alcohol. The most common anatomical location of the tear in Boerhaave syndrome is at left posterolateral wall of the lower third of the esophagus, 2-3 cm before the
stomach.
Treatment
Its treatment includes immediate
antibiotic therapy to prevent
mediastinitis and sepsis, surgical repair of the perforation, and if there is significant fluid loss it should be replaced with
IV fluid therapy since oral rehydration is, obviously, not possible.
Notes
1. S. Herman, H. Shanies, H. Singh & M. Warshawsky: "Spontaneous Esophageal Rupture: Boerhaave's Syndrome," pages 177-182. Clinical Pulmonary Medicine 10(3), May 2003
References
★
Cecil Textbook of Medicine
★
The Oxford Textbook of Medicine