Pancreatic arteriovenous malformations as a manifestation of hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease): a systematic review.

ABSTRACT:

Objectives

Limited data are available on pancreatic arteriovenous malformations (AVMs) in patients with hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber disease. This systematic review aimed to identify all reported cases of pancreatic AVMs in patients with HHT and summarise patient demographics, clinical presentation, diagnostic modalities, treatment strategies and follow-up.

Design

Systematic review in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.

Data sources

Databases PubMed, Embase, Cochrane Library and Web of Science were systematically screened up to June 2025.

Eligibility criteria

All English-language, full-text studies reporting pancreatic AVMs in patients with H

SUBMITTER: de Jager I 

PROVIDER: S-EPMC13629951 | biostudies-literature | 2026 Sep

REPOSITORIES: biostudies-literature