| Literature DB >> 8403761 |
Abstract
The purpose of this study was to evaluate the relative merits of two physical methods of locally destroying colorectal liver metastases-interstitial laser photocoagulation (ILP) which causes thermal necrosis, and percutaneous alcohol injection (PAI) which causes cellular dehydration and coagulative necrosis. Seventy-six liver metastases in 22 patients were treated by ILP or PAI. Both techniques were performed using local anaesthesia and intravenous sedation/analgesia. Ultrasound was used to localize the tumours and guide the needles percutaneously. ILP: Up to eight 19 G needles were inserted into the tumour, and down each needle was passed a thin optical fibre; the tumour was heated using low power laser light (2 W) for 500 s from a Nd:YAG or diode laser. PAI: 0.5-1 ml of sterile 95% absolute alcohol was injected into multiple sites of the tumour using a single 19-22 G needle. Dynamic CT scan was used to evaluate the extent of treatment-induced necrosis. Ultrasound showed echogenic changes around the needles/fibre-tips during ILP and PAI; this gave a reasonable guide to the extent of thermal damage for smaller tumours during ILP, but not during PAI. ILP: 54 tumours were treated (median size 2.7 cm). Laser-induced necrosis was clearly seen 24 h after treatment as a well-defined area of non-enhancement on the dynamic CT scan; greater than 50% necrosis of tumour volume was achieved in 87% of tumours (complete necrosis was found in 52% of tumours). PAI: 22 tumours were treated (median size 1.5 cm). Dynamic CT showed patchy areas of non-enhancement in five tumours, decreased density in seven tumours, and no change in 10 tumours; complete tumour necrosis was never achieved. There were no major complications after ILP or PAI, but pain during treatment was more common and more severe with PAI. ILP is a simple, safe and effective treatment for colorectal liver metastases; PAI is relatively ineffective for these tumours (although it has been shown to be much more effective for small hepatocellular carcinomas).Entities:
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Year: 1993 PMID: 8403761 DOI: 10.1016/s0009-9260(05)80130-8
Source DB: PubMed Journal: Clin Radiol ISSN: 0009-9260 Impact factor: 2.350