Open Access
CC BY 4.0 · Endoscopy 2025; 57(S 01): E686-E687
DOI: 10.1055/a-2619-1220
E-Videos

Inadvertent portal vein stenting during endoscopic retrograde cholangiopancreatography for distal bile duct cancer: endoscopic rescue and spontaneous resolution of thrombosis

Seong-Hun Kim
1   Division of Gastroenterology, Department of Internal Medicine, Jeonbuk National University Medical School, Jeonju, Korea
,
2   Division of Biliopancreas, Department of Internal Medicine, Wonkwang University College of Medicine, Iksan, Korea
3   Institute of Wonkwang Medical Science, Iksan, Korea
› Author Affiliations

Supported by: Wonkwang University 2025
 

An 86-year-old woman with distal bile duct cancer and obstructive cholangitis presented with jaundice and a 5-kg weight loss over 1 month. She underwent endoscopic retrograde cholangiopancreatography (ERCP) for biliary decompression ([Fig. 1]). Initial selective biliary cannulation failed, prompting placement of a plastic pancreatic duct stent followed by transpancreatic septotomy. A guidewire was advanced in the presumed direction of the bile duct and contrast injection suggested biliary opacification. Assuming correct guidewire placement, a fully covered self-expandable metal stent (FCSEMS) (HANAROSTENT Biliary Full Cover Benefit, 8 mm × 6 cm; M.I. Tech, Pyeongtaek, South Korea) was deployed. Substantial resistance was encountered during stent deployment, and the contrast rapidly washed out, raising suspicion of extrabiliary placement. A contrast-enhanced computed tomography (CECT) performed 2 hours later revealed that the FCSEMS had traversed the distal bile duct mass and had been inadvertently placed in the portal vein, resulting in acute portal vein thrombosis ([Fig. 2]).

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Fig. 1 Coronal contrast-enhanced computed tomography images showing an enhancing mass (white arrow) in the distal common bile duct with upstream dilation of the intrahepatic (black arrow heads) and extrahepatic bile ducts (black arrow), suggestive of distal bile duct cancer.
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Fig. 2 Contrast-enhanced computed tomography obtained 2 hours post-endoscopic retrograde cholangiopancreatography showing maldeployed fully covered self-expandable metal stent (white arrow) in the portal vein via the distal bile duct mass, with associated portal vein thrombosis (black arrow).

An emergency ERCP was performed, during which selective biliary cannulation was achieved via needle-knife precutting. The misplaced stent was retrieved, and a new FCSEMS (HANAROSTENT Biliary Lasso Full covered, 10 mm × 6 cm; M.I. Tech) and plastic stents were successfully deployed into the bile duct ([Fig. 3], [Video 1]). The patient recovered uneventfully and was discharged 10 days later. Follow-up CECT 7 days later showed portal vein thrombosis, which had resolved spontaneously by Day 153 without anticoagulation ([Fig. 4]).

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Fig. 3 Retrieval and replacement of the fully covered self-expandable metal stent (FCSEMS). a Endoscopic image showing selective bile duct cannulation with subsequent retrieval of the maldeployed FCSEMS using forceps during emergency endoscopic retrograde cholangiopancreatography. b Fluoroscopic image demonstrating correct placement of a new FCSEMS within the bile duct.
Endoscopic rescue and spontaneous resolution of thrombosis after inadvertent portal vein stenting during endoscopic retrograde cholangiopancreatography for distal bile duct cancer.Video 1

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Fig. 4 Contrast-enhanced computed tomography. a At 7 days post- endoscopic retrograde cholangiopancreatography, demonstrating portal vein thrombosis (black arrow). b The portal vein thrombosis had spontaneously resolved by follow-up imaging on Day 153 without anticoagulant therapy.

Portal vein injury is a rare but potentially fatal complication of ERCP [1] [2]. This case underscores the importance of recognizing signs of vascular misplacement, such as rapid contrast washout and deployment resistance. Early recognition and prompt endoscopic management are critical to avoiding serious complications. Notably, the spontaneous resolution of portal vein thrombosis without anticoagulation suggests that conservative management may be appropriate in selected patients with localized, nonocclusive thrombosis.

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Conflict of Interest

The authors declare that they have no conflict of interest.


Correspondence

Hyung Ku Chon, MD, PhD
Division of Biliopancreas, Department of Internal Medicine, Wonkwang University College of Medicine
895 Muwang-ro
Iksan, Jeonbuk 54538
Korea   

Publication History

Article published online:
01 July 2025

© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany


Zoom
Fig. 1 Coronal contrast-enhanced computed tomography images showing an enhancing mass (white arrow) in the distal common bile duct with upstream dilation of the intrahepatic (black arrow heads) and extrahepatic bile ducts (black arrow), suggestive of distal bile duct cancer.
Zoom
Fig. 2 Contrast-enhanced computed tomography obtained 2 hours post-endoscopic retrograde cholangiopancreatography showing maldeployed fully covered self-expandable metal stent (white arrow) in the portal vein via the distal bile duct mass, with associated portal vein thrombosis (black arrow).
Zoom
Fig. 3 Retrieval and replacement of the fully covered self-expandable metal stent (FCSEMS). a Endoscopic image showing selective bile duct cannulation with subsequent retrieval of the maldeployed FCSEMS using forceps during emergency endoscopic retrograde cholangiopancreatography. b Fluoroscopic image demonstrating correct placement of a new FCSEMS within the bile duct.
Zoom
Fig. 4 Contrast-enhanced computed tomography. a At 7 days post- endoscopic retrograde cholangiopancreatography, demonstrating portal vein thrombosis (black arrow). b The portal vein thrombosis had spontaneously resolved by follow-up imaging on Day 153 without anticoagulant therapy.