Stephanie Romutis, Anna Evans Phillips, Anil K Dasyam, Mordechai Rabinovitz, Mary Lou Klem, Charles Gabbert, Jennifer Chennat, Asif Khalid, Rohit Das, Robert Feldman, Harkirat Singh, Dhiraj Yadav, Adam Slivka, Natalie E Griffin, Morgan Ferrell, Sultan Mahmood
Journal: Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2024;24(6):870-877
PMID: 39147659
BACKGROUND
Spontaneous pancreatic portal vein fistula (PPVF) - a rare complication of pancreatic inflammation - varies widely in presentation and means of diagnosis but has been previously associated with bleeding complications and mortality. A systematic review of published literature was performed to assess the frequency of outcomes.
METHODS
A search of electronic databases (PubMed, Ovid MEDLINE, Scopus, EMBASE, gray literature) resulted in 1667 relevant unique manuscripts; 52 met inclusion criteria.
RESULTS
A total of 74 unique (male n = 47, 63.5 %) patients were included. Mean age was 53.5 (±11.9) years. History of alcohol use was reported in 55 (74.3 %). Underlying chronic pancreatitis (CP) was present in 49 (66.2 %). In cases where presenting symptoms were reported (n = 57, 77.4 %), the most frequent were abdominal pain (63.5 %), weight loss (14.9 %), rash (12.2 %), nausea/vomiting (12.2 %), and polyarthritis (9.5 %). Computed tomography was the most common imaging modality used to confirm the diagnosis (n = 20, 27.0 %), followed by magnetic resonance cholangiopancreatography (n = 14, 18.9 %). Portal vein thrombosis was reported in 57 (77.0 %), and bleeding events (luminal, variceal, or intra-pseudocyst) were reported in 13(17.6 %) patients. Younger age was associated with higher risk of bleeding events. Mortality was reported in 12 (16.2 %) patients at any time during follow up. Older age and polyarthritis at presentation were associated with mortality.
CONCLUSIONS
PPVF is a rare and potentially fatal condition, though rates of bleeding complication and death were relatively low in this population. High-quality observational studies are needed to better understand the pathophysiology and natural history of this diagnosis.
Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.
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