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. 2024 Apr 25;14(9):894. doi: 10.3390/diagnostics14090894

Table 2.

Distribution of microvascular invasion and tumour characteristics per intensity of des-γ-carboxy prothrombin labelling in liver lesions of hepatocellular carcinoma.

All Lesions (n = 119) Negative Labelling (n = 58) Focally Positive Labelling (n = 27) Diffusely Positive Labelling (n = 34) p a
Medians (IQR) or n (%)
Maximum diameter (mm) 12 (9–21) 12 (7–18) 12 (8–18) 20 (12–26) 0.002 b
Microvascular invasion (presence) 44 (37.0) 11 (19.0) 13 (48.1) 20 (58.8) <0.001
Differentiation
No tumour residue 20 (16.8) 20 (34.5) 0 (0.0) 0 (0.0) <0.001
Low-grade dysplasia 2 (1.7) 2 (3.4) 0 (0.0) 0 (0.0) 0.343
High-grade dysplasia 1 (0.8) 1 (1.7) 0 (0.0) 0 (0.0) 0.588
Well-differentiated tumour 17 (14.3) 12 (20.7) 3 (11.1) 2 (5.9) 0.127
Moderately differentiated tumour 65 (54.6) 17 (29.3) 21 (77.8) 27 (79.4) <0.001
Poorly differentiated tumour 10 (8.4) 5 (8.6) 3 (11.1) 2 (5.9) 0.763
Features of CCC or mixed HCC-CCC 4 (3.4) 1 (1.7) 0 (0.0) 3 (8.8) 0.103

The values of p that are statistically significant are reported in bold. a Kruskal–Wallis tests for quantitative variables and Χ2 tests for nominal variables; b Dunn’s multiple comparisons test for negative labelling vs. diffusely positive labelling p = 0.003 and for focally positive labelling vs. diffusely positive labelling p = 0.023. Abbreviations: CCC, cholangiocellular carcinoma; HCC, hepatocellular carcinoma.