Syndrome Capillary Malformation- Arteriovenous-Malformation (CM-AVM) : revue de la littérature

2021 ◽  
Vol 1 (8) ◽  
pp. A207-A208
Author(s):  
Adèle Essemilaire ◽  
Serge Bracard ◽  
Laetitia Goffinet ◽  
Jean-Luc Schmutz ◽  
Anne-Claire Bursztejn
Keyword(s):  
Arteriovenous Malformation ◽  
Revue De La Littérature ◽  
Capillary Malformation

A case of capillary malformation‐arteriovenous malformation and Ebstein’s anomaly in a child with EphB4 mutation

2021 ◽  
Author(s):  
Yousuf Sherwani ◽  
Samantha Jenkins ◽  
Ayodele Adelanwa ◽  
David Marshall Burch ◽  
Nita Ray Chaudhuri ◽  
...  
Keyword(s):  
Arteriovenous Malformation ◽  
Ebstein’S Anomaly ◽  
Ebstein's Anomaly ◽  
Capillary Malformation

Capillary malformation–arteriovenous malformation syndrome: Identification of a family with a novel mutation

2012 ◽  
Vol 67 (6) ◽  
pp. e287-e289 ◽  
Author(s):  
Lynn M. Boyden ◽  
Charisse M. Orme ◽  
Richard J. Antaya ◽  
Keith A. Choate ◽  
Brett A. King
Keyword(s):  
Arteriovenous Malformation ◽  
Novel Mutation ◽  
Malformation Syndrome ◽  
Capillary Malformation

Capillary malformation−arteriovenous malformation syndrome: a multicentre study

2020 ◽  
Author(s):  
M. Valdivielso‐Ramos ◽  
A. Martin‐Santiago ◽  
J. M. Azaña ◽  
A. Hernández‐Nuñez ◽  
A. Vera ◽  
...  
Keyword(s):  
Multicentre Study ◽  
Arteriovenous Malformation ◽  
Malformation Syndrome ◽  
Capillary Malformation

A Typical Vascular and Pigmentary Dermoscopic Pattern of Capillary Malformations in Capillary Malformation-Arteriovenous Malformation Syndrome: Report of Four Cases

2016 ◽  
Vol 33 (5) ◽  
pp. e337-e341 ◽  
Author(s):  
Claudine Gandon ◽  
Bertille Bonniaud ◽  
Evelyne Collet ◽  
Sophie Dalac ◽  
Géraldine Jeudy ◽  
...  
Keyword(s):  
Arteriovenous Malformation ◽  
Malformation Syndrome ◽  
Capillary Malformation ◽  
Syndrome Report

Histopathological hallmarks of cutaneous lesions of capillary malformation–arteriovenous malformation syndrome

2020 ◽  
Vol 34 (10) ◽  
pp. 2428-2435 ◽  
Author(s):  
M. Valdivielso‐Ramos ◽  
A. Torrelo ◽  
A. Martin‐Santiago ◽  
A. Hernández‐Nuñez ◽  
J.M. Azaña ◽  
...  
Keyword(s):  
Arteriovenous Malformation ◽  
Cutaneous Lesions ◽  
Malformation Syndrome ◽  
Capillary Malformation

Parkes Weber syndrome—Diagnostic and management paradigms: A systematic review

2016 ◽  
Vol 32 (6) ◽  
pp. 371-383 ◽  
Author(s):  
Igor Banzic ◽  
Milos Brankovic ◽  
Živan Maksimović ◽  
Lazar Davidović ◽  
Miroslav Marković ◽  
...  
Keyword(s):  
Systematic Review ◽  
Arteriovenous Malformation ◽  
Clinical Improvement ◽  
Venous Malformation ◽  
Lymphatic Malformation ◽  
Treatment Modalities ◽  
Eligibility Criteria ◽  
Capillary Malformation ◽  
Weber Syndrome ◽  
Klippel Trenaunay Syndrome

Objectives Parkes Weber syndrome is a congenital vascular malformation which consists of capillary malformation, venous malformation, lymphatic malformation, and arteriovenous malformation. Although Parkes Weber syndrome is a clinically distinctive entity with serious complications, it is still frequently misdiagnosed as Klippel–Trenaunay syndrome that consists of the triad capillary malformation, venous malformation, and lymphatic malformation. Methods We performed a systematic review investigating clinical, diagnostic, and treatment modalities of Parkes Weber syndrome (PubMed/MEDLINE, Embase, and Cochrane databases). Thirty-six publications (48 patients) fulfilled the eligibility criteria. Results The median age of patients was 23 years (IQR, 8–32), and 24 (50.0%) were males. Lower extremity was affected in 42 (87.5%) and upper extremity in 6 (12.5%) patients; 15 (31.3%) patients developed high-output heart failure; 12 (25.0%) patients had chronic venous ulcerations, whereas 4 (8.3%) manifested distal arterial ischemia. The spinal arteriovenous malformations were reported in six (12.5%) patients and coexistence of aneurysmatic disease in five (10.4%) patients. The most frequently utilized invasive treatments were embotherapy followed by amputation and surgical arteriovenous malformation resection, and occasionally stent-graft implantation. All modalities showed clinical improvement. However, long follow-up and outcome remained unclear. Conclusion A diagnosis of Parkes Weber syndrome should be made on the presence of capillary malformation, venous malformation, lymphatic malformation, and arteriovenous malformation (as main defect) in overgrowth extremity. Arteriovenous malformation presents the criterion for distinguishing Parkes Weber syndrome from Klippel-Trenaunay syndrome, which is substantial for treatment strategy. The primary management goal should be patient's quality of life improvement and complication reduction. Embolization alone/combined with surgical resection targeting occlusion or removal of arteriovenous malformation “nidus” reliably leads to clinical improvement.

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