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American Journal of Medical Case Reports. 2020, 8(4), 110-111
DOI: 10.12691/AJMCR-8-4-5
Case Report

An Interesting Case of Gastrointestinal Bleeding Resulting from Dieulafoy’s Lesion

Krithika Suresh1, , Daniel Ortolano2, Amir Ashiq1 and Suril Patel1

1Conemaugh Memorial Medical Center, Johnstown, PA, USA

2Conemaugh Memorial Medical Center Johnstown, PA, USA

Pub. Date: February 22, 2020

Cite this paper

Krithika Suresh, Daniel Ortolano, Amir Ashiq and Suril Patel. An Interesting Case of Gastrointestinal Bleeding Resulting from Dieulafoy’s Lesion. American Journal of Medical Case Reports. 2020; 8(4):110-111. doi: 10.12691/AJMCR-8-4-5

Abstract

Dieulafoy’s lesion (DL) is a relatively rare, but potentially life-threatening condition. It accounts for 1-2% of acute Gastrointestinal (GI) bleeding. DL is an uncommon, but important cause of gastrointestinal bleeding in which hemorrhage occurs from a pinpoint, non-ulcerated arterial lesion. [1] DLs are usually located in the stomach, most commonly in people between the ages 50 and 70 years. [2] We present a case of GI bleeding resulting from Dieulafoy lesion of the stomach, successfully treated with endoscopic intervention.

Keywords

Dieulafoy’s lesion (DL), Gastrointestinal (GI) bleed, endoscopy

Copyright

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References

[1]  Bilal M, Kapetanos A, Khan HA, Thakkar S. Bleeding "Dieulafoy's-like" lesion resembling the duodenal papilla: a case report. J Med Case Rep. 2015 May 23; 9: 118.
 
[2]  Jeon HK, Kim GH. Endoscopic Management of Dieulafoy's Lesion. Clin Endosc. 2015 Mar; 48(2): 112-20.
 
[3]  Baxter M, Aly EH. Dieulafoy's lesion: current trends in diagnosis and management. Ann R Coll Surg Engl. 2010 Oct; 92(7): 548-54.
 
[4]  Cardoso MF, Lourenço LC, Antunes M, Carvalho E Branco J, Santos L, Martins A, Reis JA. Recurrent Gastrointestinal Bleeding from Dieulafoy's Lesions in a Patient with Type 1 von Willebrand Disease: A Rare Association. GE Port J Gastroenterol. 2019 May; 26(3): 202-206.