Feasibility and safety of non-operative management of portal vein aneurysms: a thirty-five year experience.


Journal

HPB : the official journal of the International Hepato Pancreato Biliary Association
ISSN: 1477-2574
Titre abrégé: HPB (Oxford)
Pays: England
ID NLM: 100900921

Informations de publication

Date de publication:
01 2021
Historique:
received: 07 01 2020
revised: 18 03 2020
accepted: 13 05 2020
pubmed: 21 6 2020
medline: 26 10 2021
entrez: 21 6 2020
Statut: ppublish

Résumé

Portal vein aneurysms (PVAs) are rare, though clinically challenging with post-operative mortality approaching 20% and no evidence-based treatment guidelines. We aim to describe our experience with PVAs and recommend optimum management strategies. Demographics and clinical details of patients with PVAs admitted to our institution from 1984 to 2019 were reviewed. Clinical presentation, management and outcomes were analysed. PVAs were identified in 18 patients (median age 56 years, range 20-101 years; 13 female); 10 were incidental and 8 diagnosed during abdominal pain work-up. Median aneurysm diameter at diagnosis was 3.4 cm (1.8-5.5 cm), remaining unchanged at 3.5 cm (1.9-4.8 cm) during a 3.2-year follow-up (4 months-31 years). Aneurysm sites were the main portal vein (n = 12), porto-splenic-junction (n = 3), splenic-SMV-junction (n = 2) and right portal vein (n = 1). Thrombosis occurred in 4 patients; 3 developed clinically insignificant cavernous transformation. Two patients underwent surgery for abdominal pain. Postoperatively, one developed PV thrombosis and PVA recurrence occurred in the second. No aneurysm ruptures or mortalities occurred during follow-up. PVAs follow a clinically indolent course with structural stability and minimal complications over time. Non-operative management is feasible for most patients. Abdominal pain, large size or thrombosis don't appear to confer additional risks and should not, in isolation, merit surgical intervention.

Sections du résumé

BACKGROUND
Portal vein aneurysms (PVAs) are rare, though clinically challenging with post-operative mortality approaching 20% and no evidence-based treatment guidelines. We aim to describe our experience with PVAs and recommend optimum management strategies.
METHODS
Demographics and clinical details of patients with PVAs admitted to our institution from 1984 to 2019 were reviewed. Clinical presentation, management and outcomes were analysed.
RESULTS
PVAs were identified in 18 patients (median age 56 years, range 20-101 years; 13 female); 10 were incidental and 8 diagnosed during abdominal pain work-up. Median aneurysm diameter at diagnosis was 3.4 cm (1.8-5.5 cm), remaining unchanged at 3.5 cm (1.9-4.8 cm) during a 3.2-year follow-up (4 months-31 years). Aneurysm sites were the main portal vein (n = 12), porto-splenic-junction (n = 3), splenic-SMV-junction (n = 2) and right portal vein (n = 1). Thrombosis occurred in 4 patients; 3 developed clinically insignificant cavernous transformation. Two patients underwent surgery for abdominal pain. Postoperatively, one developed PV thrombosis and PVA recurrence occurred in the second. No aneurysm ruptures or mortalities occurred during follow-up.
CONCLUSION
PVAs follow a clinically indolent course with structural stability and minimal complications over time. Non-operative management is feasible for most patients. Abdominal pain, large size or thrombosis don't appear to confer additional risks and should not, in isolation, merit surgical intervention.

Identifiants

pubmed: 32561177
pii: S1365-182X(20)31021-2
doi: 10.1016/j.hpb.2020.05.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

127-133

Informations de copyright

Copyright © 2020 International Hepato-Pancreato-Biliary Association Inc. Published by Elsevier Ltd. All rights reserved.

Auteurs

Ola Ahmed (O)

Department of Abdominal Organ Transplantation Surgery, Washington University School of Medicine, St Louis, MO, USA.

John W Ohman (JW)

Department of Vascular Surgery, Washington University School of Medicine, St. Louis, MO, USA.

Neeta Vachharajani (N)

Department of Abdominal Organ Transplantation Surgery, Washington University School of Medicine, St Louis, MO, USA.

Motoyo Yano (M)

Mallinckrodt Institute of Radiology, Washington University School of Medicine, St Louis, MO, USA.

Dominic E Sanford (DE)

Department of Hepatobiliary, Pancreatic, And Gastrointestinal Surgery, Washington University School of Medicine, St. Louis, MO, USA.

Chet Hammill (C)

Department of Hepatobiliary, Pancreatic, And Gastrointestinal Surgery, Washington University School of Medicine, St. Louis, MO, USA.

Ryan C Fields (RC)

Department of Hepatobiliary, Pancreatic, And Gastrointestinal Surgery, Washington University School of Medicine, St. Louis, MO, USA.

William G Hawkins (WG)

Department of Hepatobiliary, Pancreatic, And Gastrointestinal Surgery, Washington University School of Medicine, St. Louis, MO, USA.

Steven M Strasberg (SM)

Department of Hepatobiliary, Pancreatic, And Gastrointestinal Surgery, Washington University School of Medicine, St. Louis, MO, USA.

Maria B Doyle (MB)

Department of Abdominal Organ Transplantation Surgery, Washington University School of Medicine, St Louis, MO, USA.

William C Chapman (WC)

Department of Abdominal Organ Transplantation Surgery, Washington University School of Medicine, St Louis, MO, USA.

Adeel S Khan (AS)

Department of Abdominal Organ Transplantation Surgery, Washington University School of Medicine, St Louis, MO, USA. Electronic address: akhan24@wustl.edu.

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