Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2023 Aug 16;4(4):e347.
doi: 10.1097/PG9.0000000000000347. eCollection 2023 Nov.

Avoiding Surgery: Endoscopic Treatment of Congenital Duodenal Stenosis

Affiliations
Case Reports

Avoiding Surgery: Endoscopic Treatment of Congenital Duodenal Stenosis

Jessica V Baran et al. JPGN Rep. .

Abstract

Duodenal stenosis is a rare congenital anomaly that is typically treated surgically, although endoscopic incisional therapy (EIT) and balloon dilation are minimally invasive alternatives. We present a case of a 15-month-old male with vomiting and difficulty tolerating solid food due to severe congenital duodenal stenosis. The patient underwent EIT and serial duodenal dilation to a diameter of 20 mm, which resulted in significant symptom improvement. Intralesional corticosteroid injection (ISI) was administered to help prevent the duodenal septum from restricturing. The combination of EIT, balloon dilation, and ISI was successful in treating the patient's congenital duodenal stenosis and avoided the need for surgery. However, further studies are required to confirm the efficacy of this treatment approach in this patient population. This report highlights the potential of this minimally invasive approach as an alternative to surgical intervention in the management of congenital duodenal stenosis.

Keywords: endoscopic balloon dilation; endoscopy; intralesional corticosteroid injection; membranous duodenal web; radial incisional therapy.

PubMed Disclaimer

Conflict of interest statement

The authors report no conflicts of interest.

Figures

FIGURE 1.
FIGURE 1.
Fluoroscopic UGI series images showing: (A) “Double-bubble sign” with proximal duodenum dilated to 5.5 cm in diameter; and (B) high-grade duodenal obstruction associated with severe duodenal stenosis (arrow).
FIGURE 2.
FIGURE 2.
Significant duodenal dilation (A) noted proximal to the duodenal stenosis with pinhole orifice (B) just distal to the Ampulla of Vater on initial endoscopy. Bile was noted to pool (C) in the dilated duodenum. (B) Close-up view of pinhole orifice of the duodenal stenosis (arrow). (C) Endoscopic image showing balloon dilation of severe duodenal stenosis. (D) Patent duodenal orifice, status post endoscopic incisional therapy, and balloon dilation to 20 mm.

References

    1. Williams SA, Nguyen ATH, Chang H, et al. . Multicenter comparison of laparoscopic versus open repair of duodenal atresia in neonates. J Laparoendosc Adv Surg Tech A. 2022;32:226–230. - PubMed
    1. Poddar U, Jain V, Yachha SK, et al. . Congenital duodenal web: successful management with endoscopic dilatation. Endosc Int Open. 2016;4:E238–E241. - PMC - PubMed
    1. Huang MH, Bian HQ, Liang C, et al. . Gastroscopic treatment of membranous duodenal stenosis in infants and children: report of 6 cases. J Pediatr Surg. 2015;50:413–416. - PubMed
    1. Beeks A, Gosche J, Giles H, et al. . Endoscopic dilation and partial resection of a duodenal web in an infant. J Pediatr Gastroenterol Nutr. 2009;48:378–381. - PubMed
    1. Muensterer OJ, Hansen EN. Resection of a duodenal web using single-incision pediatric endosurgery. J Pediatr Surg. 2011;46:989–993. - PubMed

Publication types