Percutaneous image-guided cryoablation of umbilical endometriosis: safety, feasibility, clinical, and imaging outcomes
Percutaneous image-guided cryoablation for umbilical endometriosis achieved 82% pain relief, 73% nodule volume reduction, and high cosmetic satisfaction with predominantly minor adverse events.
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This single-institution study evaluated the safety, feasibility, and outcomes of percutaneous image-guided cryoablation for umbilical endometriosis in 17 women treated between 2017 and 2024, using ultrasound-only or combined ultrasound/CT guidance. Pain was measured with a visual analog scale and imaging with ultrasound and MRI, with cosmetic outcomes assessed before and after treatment; adverse events were graded using the Society of Interventional Radiology classification. Complete pain relief occurred in 14/17 patients (82%) at a median follow-up of 22 months, median VAS decreased from 8.0 to 0.0 (p<0.001), and MRI nodule volume decreased from 2.98 cm³ to 0.90 cm³ with a median individual reduction of 73.0%; cosmetic satisfaction was reported in 14/17 (82%). The paper’s main limitation is the small, single-arm cohort without a control group, which constrains comparative conclusions. This paper is centrally about endometriosis — specifically percutaneous cryoablation for umbilical endometriosis with reported safety, pain, imaging, and cosmetic outcomes.
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