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2026, Number 4

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Acta Med 2026; 24 (4)

Bouveret syndrome

Castro RR, Paredes VJE
Full text How to cite this article 10.35366/123522

DOI

DOI: 10.35366/123522
URL: https://dx.doi.org/10.35366/123522

Language: Spanish
References: 4
Page: 478-480
PDF size: 1043.13 Kb.


Key words:

Bouveret's syndrome, gallstone ileus, Mirizzi’s syndrome, bowel obstruction, Rigler's triad.

ABSTRACT

Bouveret syndrome is a very rare form of gastric outlet obstruction following the passage of a gallstone from the gallbladder to the duodenum or pylorus through a bilioenteric fistula. This rare syndrome was first described in 1896 by Leon Bouveret, a French physician, which since then bears his name. A classic Rigler’s triad of dilated stomach, pneumobilia, and ectopic stone appearing as a filling defect in the duodenum seen on a CT scan is virtually pathognomonic of the Bouveret’s syndrome. The primary therapeutic goal is gallstone retrieval.


REFERENCES

  1. Philipose J, Khan HM, Ahmed M, Idiculla PS, Andrawes S.Bouveret’s syndrome. Cureus. 2019; 11 (4): e4414. doi: 10.7759/cureus.4414.

  2. Haddad FG, Mansour W, Deeb L. Bouveret’s syndrome: literaturereview. Cureus. 2018; 10 (3): e2299. doi: 10.7759/cureus.2299.

  3. Koulaouzidis A, Moschos J. Bouveret’s syndrome. Narrative review.Ann Hepatol. 2007; 6 (2): 89-91.

  4. Thatipalli N, Gattani R, Nayak K, Sudabattula K. Bouveret syndrome:etiology, clinical presentation, differential diagnosis, complications,and treatment options. Cureus. 2024; 16 (7): e64754. doi: 10.7759/cureus.64754.




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Acta Med. 2026;24