[Microwave coagulation at different temperatures for hepatocellular carcinoma management: efficacy evaluation by enzyme histochemical staining].

Nan Fang Yi Ke Da Xue Xue Bao

Department of Hepatobiliary Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.

Published: August 2006

AI Article Synopsis

  • The study aimed to evaluate the effectiveness of HE staining versus enzyme histochemical staining in assessing the viability of hepatocellular carcinoma (HCC) cells after microwave ablation at different temperatures.
  • Two groups of mice with transplanted HCC were treated with microwave ablation at 60°C and 50°C, and tissue samples were analyzed before and after the procedure using both staining methods.
  • Results showed that while HE staining revealed no significant changes in cell morphology, enzyme histochemical staining indicated complete cell death at 60°C and some surviving cells at 50°C, highlighting the superiority of enzyme staining for assessing tumor cell viability post-ablation.

Article Abstract

Objective: To compare the application of HE and enzyme histochemical staining in assessing the viability of hepatocellular carcinoma (HCC) cells coagulated by microwave ablation at different temperatures.

Methods: Two groups of mice (n=6) with transplanted homogenic HCC were treated by microwave ablation at 60 degrees C and 50 degrees C for 3 min, respectively. Before and after microwave ablation, paraffin sections and frozen sections of the tumors were prepared for routine HE staining and enzyme histochemical staining with nicotinamide adenine dinucleotide diaphorase (NADH-diaphorase), respectively, and observed under microscope.

Results: Shortly after microwave ablation, the morphology and arrangements of the nucleus of the ablated tumor cells in the two groups showed no obvious alteration in HE stained sections, but in sections with enzyme histochemical staining, the activity of NADH-diaphorase in ablated tumor tissue at 60 degrees C disappeared, suggesting the death of HCC cells; sporadic activity of the enzyme was detected in the coagulated tumor at 50 degrees C, indicating tumor cells surviving the ablation. The ablation effect was markedly different between the two groups (P<0.01).

Conclusion: HE staining is not suitable for evaluation of HCC destruction immediately after microwave ablation, and detection of NADH-diaphorase activity with the enzyme histochemical method better suits this purpose.

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