Peripheral Vascular Malformations: Imaging, Treatment Approaches, and Therapeutic Issues
- 1 October 2005
- journal article
- review article
- Published by Radiological Society of North America (RSNA) in RadioGraphics
- Vol. 25 (suppl_1) , S159-S171
- https://doi.org/10.1148/rg.25si055509
Abstract
Peripheral vascular malformations are now described according to some accepted guidelines, and the principle of proper treatment (nidus ablation) is becoming clear. An appropriate classification scheme for vascular anomalies and definite indications for treatment are important to successful treatment overall. The findings from noninvasive imaging (ie, Doppler ultrasonography, computed tomography, or magnetic resonance imaging) in association with clinical findings are critical in establishing the diagnosis, evaluating the extent of the malformation, and planning appropriate treatment. Direct opacification of the nidus is useful, not only in making a correct diagnosis, but also in treating the lesion with sclerotherapy. In most cases, conservative treatment is recommended, but when a patient suffers clinical complications (eg, ulceration, pain, hemorrhage, cardiac failure, or unacceptable cosmetic consequences), the nidus sclerotherapy becomes mandatory. If the vascular malformation has blood outflow to a drainage vein during nidus opacification, flow control (with balloon occlusion, tourniquet, or embolization) is necessary to achieve sclerosant stasis within the nidus. Embolotherapy (with a coil, n-butyl cyanoacrylate, or small particles) should be used for subsequent multifaceted palliative therapy. A multi-disciplinary approach is needed in the treatment of a high-flow lesion, and a dedicated team approach is necessary for appropriate management in most cases.Keywords
This publication has 36 references indexed in Scilit:
- Low-Flow Vascular Malformations: MR-guided Percutaneous Sclerotherapy in Qualitative and Quantitative Assessment of Therapy and OutcomeRadiology, 2004
- Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st centuryPostgraduate Medical Journal, 2003
- Soft-Tissue Venous Malformations in Adult Patients: Imaging and Therapeutic IssuesRadioGraphics, 2001
- Evaluation of flow characteristics of soft-tissue vascular malformations using technetium-99m labelled red blood cells.European Journal of Nuclear Medicine and Molecular Imaging, 1999
- Classification and Management of the Various Superficial Vascular Anomalies: Hemangiomas and Vascular MalformationsThe Journal of Dermatology, 1997
- Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2Nature Genetics, 1996
- Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1Nature Genetics, 1994
- Hemangiomas, Vascular Malformations, and Lymphovenous MalformationsPlastic and Reconstructive Surgery, 1993
- Mucocutaneous and peripheral soft-tissue hemangiomas: MR imaging.Radiology, 1987
- Hemangiomas and Vascular Malformations in Infants and ChildrenPlastic and Reconstructive Surgery, 1982