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Updated: Oct 15, 2025

A Patient-Derived Xenograft Model for Venous Malformation
Published on: June 15, 2020
Venous Malformations in Childhood: Clinical, Histopathological and Genetics Update
Isabel Colmenero1, Nicole Knöpfel2,3
1Department of Pathology, Hospital Infantil Universitario Niño Jesús, 28009 Madrid, Spain.
Abstract:
Our knowledge in vascular anomalies has grown tremendously in the past decade with the identification of key molecular pathways and genetic mutations that drive the development of vascular tumors and vascular malformations. This has led us to better understand the pathogenesis of vascular lesions, refine their diagnosis and update their classification while also exploring the opportunity for a targeted molecular treatment. This paper aims to provide an overview of venous malformations (VM) in childhood. Specific entities include common VMs, cutaneo-mucosal VM, blue rubber bleb nevus syndrome or Bean syndrome, glomuvenous malformation, cerebral cavernous malformation, familial intraosseous vascular malformation and verrucous venous malformation. The clinicopathological features and the molecular basis of each entity are reviewed.
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