Cryoablation in fibro-adipose vascular anomaly (FAVA): a minimally invasive treatment option
Background Fibro-adipose vascular anomaly (FAVA) is a complex vascular malformation that typically presents with persistent pain, discomfort, contracture and other disabling symptoms. There are no minimally invasive treatment options to effectively control these symptoms. Image-guided percutaneous c...
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Veröffentlicht in: | Pediatric radiology 2016-07, Vol.46 (8), p.1179-1186 |
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Sprache: | eng |
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Zusammenfassung: | Background
Fibro-adipose vascular anomaly (FAVA) is a complex vascular malformation that typically presents with persistent pain, discomfort, contracture and other disabling symptoms. There are no minimally invasive treatment options to effectively control these symptoms. Image-guided percutaneous cryoablation, which has been used to control pain in people with cancer, could be used for similar indications in FAVA.
Objective
To assess the role of image-guided percutaneous cryoablation for control of symptoms in FAVA lesions.
Materials and methods
We conducted a retrospective cohort study of 20 children and young adults with FAVA who underwent percutaneous cryoablation at 26 sites, from September 2013 to August 2015. The outcome was based on the brief pain inventory scoring (BPI), concurrent symptoms, clinical response and patient satisfaction.
Results
After cryoablation there was significant improvement in pain, which dropped by 3 points (pain now) to 3.7 points (pain in the last 24 h). Most patients indicated that pain interfered less in their everyday social life. Concurrent symptoms like swelling, physical limitations and skin hyperesthesia also improved. Clinical response was greatest at 2–5 months follow-up after cryoablation, with acceptable patient satisfaction thereafter. Technical response was 100%. There were no major complications.
Conclusion
Image-guided percutaneous cryoablation is a safe and effective option for treatment of symptomatic FAVA lesions. |
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ISSN: | 0301-0449 1432-1998 |
DOI: | 10.1007/s00247-016-3576-0 |