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Molecular Pathways and Possible Therapies for Head and Neck Vascular Anomalies

Authors :
UCL - SSS/DDUV/GEHU - Génétique
UCL - (SLuc) Service de chirurgie plastique
Coulie, Julien
Boon, Laurence
Vikkula, Miikka
UCL - SSS/DDUV/GEHU - Génétique
UCL - (SLuc) Service de chirurgie plastique
Coulie, Julien
Boon, Laurence
Vikkula, Miikka
Source :
Journal of Oral Pathology & Medicine, (2022)
Publication Year :
2022

Abstract

Vascular Anomalies are a heterogenous group of vascular lesions that can be divided, according to the International Society for the Study of Vascular Anomalies Classification, into two main groups : Vascular Tumors and Vascular Malformations. Vascular Malformations can be further subdivided into slow-flow and fast-flow malformations. This clinical and radiologica l classification allows for a better understanding of vascular anomalies and aims to offer a more precise final diagnosis. Correct diagnosis is essential to propose the best treatment, which traditionally consists of surgery, embolization or sclerotherapy. Since a few years, medical treatment has become an important part of multidisciplinary treatment. Genetic and molecular knowledge of vascular anomalies are increasing rapidly and opens the door for a molecular classification of vascular anomalies according to the underlying pathways involved. The main pathways seem to be: PI3K/AKT/mTOR (PIKopathies) and RAS/RAF/MEK/ERK (RASopathies). Knowing the underlying molecular cascades allows us to use targeted medical therapies. The first part of this article aims to review the vascular anomalies seen in the head and neck region and their underlying molecular causes and involved pathways. The second part will propose an overview of the available targeted therapies based on the affected molecular cascade. This article summarizes theragnostic treatments available in vascular anomalies.

Details

Database :
OAIster
Journal :
Journal of Oral Pathology & Medicine, (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372961302
Document Type :
Electronic Resource