S4142 Hemobilia Secondary to Choledochal Varices: A Rare Cause of GI Bleeding Managed Endoscopically With Biliary Stenting

Introduction: Choledochal varices are an uncommon cause of hemobilia and can mimic neoplasia on cross-sectional imaging, especially during active bleeding or in the presence of an intraductal blood clot. Historically, management has been with portosystemic shunting. Case Description/Methods: A 68-year-old man was admitted to our system with new, worsening abdominal distention and abdominal pain. On computed tomography (CT), notable findings included cirrhotic liver morphology, large-intra-abdominal ascites, a portal venous thrombus with cavernous transformation, an ill-defined hypoattenuation near the portal venous thrombus concerning for a mass, and pancreatic calcification suggestive of chronic pancreatitis. The patient was found to be hepatitis C positive and did endorse a longstanding alcohol abuse. During his admission, the patient also developed melena with an acute hemoglobin decline to 11.4 g/dL. After a multi-disciplinary discussion, the decision was made to pursue esophagogastroduodenoscopy (EGD) evaluation for melena; endoscopic ultrasound (EUS) to evaluate the hypoattenuation on CT scan; and endoscopic retrograde cholangiopancreatography (ERCP) with cholangioscopy. Aside from small, non-bleeding esophageal varices and portal hypertensive gastropathy, the EGD was unremarkable. On EUS, there was well-defined, heteroechoic lesion within the lumen of the bile duct; the bile duct in this region was also surrounded by doppler-positive structures consistent with choledochal varices. ERCP was performed, showing a large intraductal filling defect that was freely mobile, and cholangioscopy confirmed a large blood clot, not a mass. Extraction of the clot was successful, and classic features of choledochal varices were seen on the post-extraction cholangiogram. A transpapillary fully covered metal stent was placed with resulting hemostasis and no recurrence of hemorrhage. The patient ultimately was discharged, but prior to liver transplant evaluation, he was readmitted with septic shock from aspiration pneumonia with Enterobactercloacae bacteremia and ultimately died in hospice. Discussion: Bile duct varices can cause extrinsic biliary compression (even mimicking a malignant stricture on cholangiogram) with rare cases of hemobilia described in old literature. While portosystemic shunting is the typical management strategy, we describe a successful case of endoscopic management with biliary stenting, which could be considered in patients who are poor candidates for portosystemic shunting or transplantation. Watch the video: https://tinyurl.com/25ACGS4142

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001144028.05255.d1
Primary Topic
Abdominal vascular conditions and treatments
Type
article
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article

S4142 Hemobilia Secondary to Choledochal Varices: A Rare Cause of GI Bleeding Managed Endoscopically With Biliary Stenting

Edward Villa, Paul Hong, Sarah Burroughs
The American Journal of Gastroenterology
Abdominal vascular conditions and treatments
article

S4142 Hemobilia Secondary to Choledochal Varices: A Rare Cause of GI Bleeding Managed Endoscopically With Biliary Stenting

Edward Villa, Paul Hong, Sarah Burroughs
article en

Abstract

Introduction: Choledochal varices are an uncommon cause of hemobilia and can mimic neoplasia on cross-sectional imaging, especially during active bleeding or in the presence of an intraductal blood clot. Historically, management has been with portosystemic shunting. Case Description/Methods: A 68-year-old man was admitted to our system with new, worsening abdominal distention and abdominal pain. On computed tomography (CT), notable findings included cirrhotic liver morphology, large-intra-abdominal ascites, a portal venous thrombus with cavernous transformation, an ill-defined hypoattenuation near the portal venous thrombus concerning for a mass, and pancreatic calcification suggestive of chronic pancreatitis. The patient was found to be hepatitis C positive and did endorse a longstanding alcohol abuse. During his admission, the patient also developed melena with an acute hemoglobin decline to 11.4 g/dL. After a multi-disciplinary discussion, the decision was made to pursue esophagogastroduodenoscopy (EGD) evaluation for melena; endoscopic ultrasound (EUS) to evaluate the hypoattenuation on CT scan; and endoscopic retrograde cholangiopancreatography (ERCP) with cholangioscopy. Aside from small, non-bleeding esophageal varices and portal hypertensive gastropathy, the EGD was unremarkable. On EUS, there was well-defined, heteroechoic lesion within the lumen of the bile duct; the bile duct in this region was also surrounded by doppler-positive structures consistent with choledochal varices. ERCP was performed, showing a large intraductal filling defect that was freely mobile, and cholangioscopy confirmed a large blood clot, not a mass. Extraction of the clot was successful, and classic features of choledochal varices were seen on the post-extraction cholangiogram. A transpapillary fully covered metal stent was placed with resulting hemostasis and no recurrence of hemorrhage. The patient ultimately was discharged, but prior to liver transplant evaluation, he was readmitted with septic shock from aspiration pneumonia with Enterobactercloacae bacteremia and ultimately died in hospice. Discussion: Bile duct varices can cause extrinsic biliary compression (even mimicking a malignant stricture on cholangiogram) with rare cases of hemobilia described in old literature. While portosystemic shunting is the typical management strategy, we describe a successful case of endoscopic management with biliary stenting, which could be considered in patients who are poor candidates for portosystemic shunting or transplantation. Watch the video: https://tinyurl.com/25ACGS4142

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 48%
Abdominal vascular conditions and treatments
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