Diagnosis and management of extensive vascular malformations of the lower limb : Part II. Systemic repercussions, diagnosis, and treatment - 14/10/11
Abstract |
At least nine types of vascular malformations with specific clinical and radiologic characteristics must be distinguished in the lower limbs: Klippel–Trénaunay syndrome, port-wine stain with or without hypertrophy, cutis marmorata telangiectatica congenita, macrocephaly–capillary malformation, Parkes Weber syndrome, Stewart–Bluefarb syndrome, venous malformation, glomuvenous malformation, and lymphatic malformation. Extensive vascular malformations are often more complex than they appear and require a multidisciplinary therapeutic approach. Vascular malformations may be associated with underlying disease or systemic anomalies. Part II of this two-part series on the diagnosis and management of extensive vascular malformations of the lower limb highlights the systemic repercussions (bone, articular, visceral, and hematologic involvement), diagnosis, and treatment of these lesions.
Le texte complet de cet article est disponible en PDF.Key words : cutis marmorata telangiectatica congenita, embolization, glomuvenous malformation, port-wine stain, Klippel-Trenaunay syndrome, laser, localized intravascular coagulation, lymphatic malformation, macrocephaly-capillary malformation, magnetic resonance, multi-detector computed tomography, Parkes Weber syndrome, pulmonary hypertension vascular malformations, Stewart-Bluefarb syndrome, sclerotherapy, surgery, venous malformation
Plan
Funding sources: None. |
Vol 65 - N° 5
P. 909-923 - novembre 2011 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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