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Optimal lesion assessment following acute radio frequency ablation of porcine kidney: cellular viability or histopathology?

作者信息

Marcovich Robert, Aldana Joel P A, Morgenstern Nora, Jacobson Avrum I, Smith Arthur D, Lee Benjamin R

机构信息

Department of Urology, Long Island Jewish Medical Center, New Hyde Park, New York, USA.

出版信息

J Urol. 2003 Oct;170(4 Pt 1):1370-4. doi: 10.1097/01.ju.0000073846.32015.45.

Abstract

PURPOSE

Radio frequency ablation (RFA) has been used as a minimally invasive alternative to nephrectomy for small renal tumors. Questions have arisen regarding the accuracy of cell viability determination on standard hematoxylin and eosin (H & E) staining. We investigated and compared the histological characteristics of RF ablated renal tissue using nicotinamide adenine dinucleotide (NADH) and H & E staining.

MATERIALS AND METHODS

Ten porcine kidneys underwent laparoscopic RFA of the upper and lower poles using a 2 (8) or 3 cm (2) protocol with 2 cycles of 90 W, target temperature 105C and treatment time 5.5 minutes per cycle. Following tract ablation the kidneys were immediately harvested, gross lesion size was measured and tissue was processed for standard H & E and NADH staining.

RESULTS

H & E staining of ablated tissue revealed a number of alterations in renal tubular histology. However, all of these findings were focal with areas of parenchyma that appeared well preserved. Corresponding areas on NADH processed sections showed the complete absence of staining, indicating the lack of cellular viability. There were no skip areas noted on NADH processed sections and treated portions demonstrated a well demarcated border of ablation.

CONCLUSIONS

While RFA produces discernible histological changes acutely on H & E, these alterations are variable and patchy, and they alternate with areas of well preserved tissue. Therefore, NADH staining should always be used to assess and verify cellular death in RFA lesions. In this study no skip areas of viable cells were noted within areas of ablated tissue on NADH staining.

摘要

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