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. Author manuscript; available in PMC: 2019 Jan 22.
Published in final edited form as: Eur Radiol. 2012 Aug 21;23(2):579–587. doi: 10.1007/s00330-012-2631-y

Table 2.

Frequency with which binary features were present in focal type 1, focal type 2 and infiltrative papillary renal cell carcinoma (pRCC), with P value obtained from univariate generalised estimating equations analysis for comparison between categories of pRCC

Feature Focal type 1 pRCCa Focal type 2 pRCCa P (focal type 1 vs. focal type 2) Infiltrative pRCCa P (infiltrative vs. all focal)
Metastatic diseaseb 3.7 (2/54) 7.5 (3/40) 0.648 75.0 (6/8) <0.001
Central location 4.6 (3/65) 5.6 (3/54) 1.0 88.9 (8/9) <0.001
Poorly encapsulated 0 (0/65) 3.7 (2/54) 0.204 100 (9/9) <0.001
Renal vein thrombus 0 (0/65) 0 (0/54) 1.0 88.9 (8/9) <0.001
Irregular margins 21.5 (14/65) 35.2 (19/54) 0.089 100 (9/9) <0.001
Perirenal invasion 6.2 (4/65) 3.7 (2/54) 0.688 55.6 (5/9) <0.001
Retroperitoneal collaterals 30.8 (20/65) 22.2 (12/54) 0.309 77.8 (7/9) 0.007
Homogeneous enhancement 46.2 (30/65) 42.6 (23/54) 0.715 11.1 (1/9) 0.084
Microscopic fatc 7.9 (5/63) 3.8 (2/53) 0.451 22.2 (2/9) 0.095
Homogeneous T2 signal intensity 35.4 (23/65) 22.2 (12/54) 0.157 11.1 (1/9) 0.264
Haemosiderinc 27.0 (17/63) 50.9 (27/53) 0.056 22.2 (2/9) 0.358
Necrosis 32.3 (21/65) 25.9 (14/54) 0.448 55.6 (5/9) 0.117
Haemorrhage 41.5 (27/65) 70.4 (38/54) 0.004 22.2 (2/9) 0.082
High grade (most common) 1.5 (1/65) 38.9 (21/54) <0.001 44.4 (4/9) 0.077
High grade (highest) 38.5 (25/65) 88.9 (48/54) <0.001 88.9 (8/9) 0.134
Stage T2/T3 11.1 (7/63) 28.0 (14/50) 0.022 87.5 (7/8) <0.001

Data listed in bold are statistically significant at P<0.05. Features not recorded in binary fashion (T2 signal intensity, enhancement in nephron-graphic phase, and cystic component) are not included in the table but did not show significant differences for any comparisons (P>0.05)

a

Data are percentages, with raw numbers in parentheses

b

Not included in patients for whom presence or absence of metastatic disease could not be determined

c

Not evaluated in three lesions imaged at 3.0 T with in-phase echo acquired before the opposed-phase echo