S4649 A Rare Case of a Portal Vein Pseudoaneurysm

Introduction: Pseudoaneurysms arise due to trauma, inflammation, infection or iatrogenic causes including procedures. The prevalence of portal venous aneurysms, which include pseudoaneurysms, is less than 0.4%. We present a case of a portal venous pseudoaneurysm secondary to a Whipple procedure that caused recurrent bleeding. Case Description/Methods: A 61-year-old woman with a past medical history of cholangiocarcinoma status post Whipple procedure with Billroth II and portal vein repair in December 2022 presented to the hospital in September 2024 with hematochezia. A computed tomography (CT) of the abdomen and pelvis (A/P) with gastrointestinal bleed (GI) protocol showed a large pseudoaneurysm at the portal vein confluence anteriorly that was 28 × 20 × 22 mm in size. Operative management was not offered due to the location of the bleed. The patient had no further drops in hemoglobin or ongoing melena and was discharged home. She represented in January and February 2025 with melena and hematochezia. Workup included a CT abdomen and pelvis which showed the portal vein pseudoaneurysm at 20 × 20 × 25 mm in size, an upper endoscopy, colonoscopy, double balloon anterograde enteroscopy and double balloon retrograde enteroscopy that were all negative for a bleed, and a video capsule endoscopy that showed an illeal angioectasia without bleeding. She was sent home on subcutaneous octreotide. She then presented from clinic due to melena. She had hematemesis that led to hemorrhagic shock. Small bowel enteroscopy showed mucosal changes in the efferent jejunum, concerning for active bleeding. A CT GI bleed did not show active bleeding. Pancreatobiliary surgery was consulted due to concern a fistula between the portal vein pseudoaneurysm and pancreaticojejenum anastomosis site. She underwent a complete pancreatectomy, portal vein reconstruction with a peritoneal patch, and a splenectomy. Discussion: Portal vein pseudoaneurysms are a rare phenomenon after a Whipple procedure. More conservative measurements were tried in this patient given the limitations of procedural management. The decision was made to send the patient home since her bleeding resolved after initial presentation with the recommendation to present back to the emergency department if she had more bleeding. She presented 3 more times for bleeding over 6 months, requiring the massive transfusion protocol and admission to the medical intensive care unit for hemorrhagic shock. Her course highlights how symptomatic a portal vein pseudoaneurysm can be, as well as the intermittent of the bleeding.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001146056.22950.db
Primary Topic
Abdominal vascular conditions and treatments
Type
article
Field-Weighted Citation Impact
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article

S4649 A Rare Case of a Portal Vein Pseudoaneurysm

Tayna Latortue, Manuel A. Amaris, Muhammad Ali, Jack Burcher
The American Journal of Gastroenterology
Abdominal vascular conditions and treatments
article

S4649 A Rare Case of a Portal Vein Pseudoaneurysm

Tayna Latortue, Manuel A. Amaris, Muhammad Ali, Jack Burcher
article en

Abstract

Introduction: Pseudoaneurysms arise due to trauma, inflammation, infection or iatrogenic causes including procedures. The prevalence of portal venous aneurysms, which include pseudoaneurysms, is less than 0.4%. We present a case of a portal venous pseudoaneurysm secondary to a Whipple procedure that caused recurrent bleeding. Case Description/Methods: A 61-year-old woman with a past medical history of cholangiocarcinoma status post Whipple procedure with Billroth II and portal vein repair in December 2022 presented to the hospital in September 2024 with hematochezia. A computed tomography (CT) of the abdomen and pelvis (A/P) with gastrointestinal bleed (GI) protocol showed a large pseudoaneurysm at the portal vein confluence anteriorly that was 28 × 20 × 22 mm in size. Operative management was not offered due to the location of the bleed. The patient had no further drops in hemoglobin or ongoing melena and was discharged home. She represented in January and February 2025 with melena and hematochezia. Workup included a CT abdomen and pelvis which showed the portal vein pseudoaneurysm at 20 × 20 × 25 mm in size, an upper endoscopy, colonoscopy, double balloon anterograde enteroscopy and double balloon retrograde enteroscopy that were all negative for a bleed, and a video capsule endoscopy that showed an illeal angioectasia without bleeding. She was sent home on subcutaneous octreotide. She then presented from clinic due to melena. She had hematemesis that led to hemorrhagic shock. Small bowel enteroscopy showed mucosal changes in the efferent jejunum, concerning for active bleeding. A CT GI bleed did not show active bleeding. Pancreatobiliary surgery was consulted due to concern a fistula between the portal vein pseudoaneurysm and pancreaticojejenum anastomosis site. She underwent a complete pancreatectomy, portal vein reconstruction with a peritoneal patch, and a splenectomy. Discussion: Portal vein pseudoaneurysms are a rare phenomenon after a Whipple procedure. More conservative measurements were tried in this patient given the limitations of procedural management. The decision was made to send the patient home since her bleeding resolved after initial presentation with the recommendation to present back to the emergency department if she had more bleeding. She presented 3 more times for bleeding over 6 months, requiring the massive transfusion protocol and admission to the medical intensive care unit for hemorrhagic shock. Her course highlights how symptomatic a portal vein pseudoaneurysm can be, as well as the intermittent of the bleeding.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 41%
Abdominal vascular conditions and treatments
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