Purpose: To evaluate the safety and effectiveness of percutaneous magnetic resonance (MR) imaging-guided laser ablation and cryoablation for the treatment of symptomatic soft tissue vascular anomalies (VAs) of the trunk and extremities.Materials and Methods: An institutional review board-approved retrospective review was undertaken of all pediatric and adult patients who underwent MR imaging-guided and monitored laser ablation and/or cryoablation for the treatment of symptomatic peripheral soft tissue VA. Preablation and postablation MR imaging was independently reviewed. Pain scores on the visual analog scale (0 to 10) and self-reported subjective symptomatic improvement were assessed. Change in VA size and pain scores were compared using a paired t test.Results: Thirty patients (24 females; age, 10-75 years) with 34 VAs were treated for moderate to severe pain (n ¼ 27) or swelling/mass effect (n ¼ 3) with 60 total ablation sessions. The baseline maximum VA diameter was 9.5 cm ± 8.6. At baseline, all VAs (100%) demonstrated variable T2-weighted signal hyperintensity and enhancement. The baseline pain score was 6.4 ± 1.6. Clinical follow-up was available for 23 patients. At a mean follow-up time of 12.2 months ± 10.1, 19 of 20 (95%) patients treated for pain and 2 of 3 (67%) patients treated for swelling/mass effect reported partial or complete symptomatic relief. There was a significant decrease in the postablation pain scores (À5.7 ± 1.0, P < .001) and maximum VA size (À2.3 cm ± 2.7, P ¼ .004), with >50% reduction in VA T2 signal (59%) and enhancement (73%). Nine of 30 (30%) patients experienced minor complications.Conclusions: MR imaging-guided and monitored percutaneous laser ablation and cryoablation appear to be safe and effective for the treatment of symptomatic peripheral soft tissue VAs.
ABBREVIATIONSPeripheral soft tissue vascular anomalies (VAs) can be classified as vascular tumors, which can be benign, locally aggressive/borderline, or malignant, or as vascular malformations, which can be further subdivided into simple or combined nonneoplastic anomalies. VAs are typically sporadic and isolated but may be associated with a number of different genetic syndromes (1). VAs may not only cause pain, swelling, or cosmetic concern but also may cause more serious, potentially life-threatening problems such as highoutput cardiac failure or consumptive coagulopathy, depending on VA size, location, histopathology, and flow characteristics (2).