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Table 1 Clinical characteristics of patients with vHL syndrome

From: Factors that predict progression of von Hippel-Lindau disease-related malignancy: a longitudinal cohort study

Characteristic

All

Missense mutation

Truncation mutation

P value

(between two groups)

Number of patients

94

84

10

 

Age (years)

37.12 ± 16.39

37.30 ± 16.34

35.60 ± 17.59

.759

Sex

 Female

49 (52.13%)

44 (52.38%)

5 (50.00%)

 > .999

 Male

45 (47.87%)

40 (47.62%)

5 (50.00%)

 

Baseline

Hemangioblastoma, brain

53 (61.63%)

47 (60.26%)

6 (75.00%)

.705

 Median number

2 (1,5)

2 (1, 5)

3.5 (1, 5)

.660

 Median volume (ml)

22 (8, 35)

   

Renal cell carcinoma

27 (30.00%)

25 (31.25%)

2 (20.00%)

.717

 Median number

2 (1, 4)

2(1, 3)

3 (1, 5)

.730

 Median volume (ml)

40 (24, 102)

40 (25, 80)

89.5 (24, 155)

.746

Hemangioblastoma, spine

43 (55.13%)

40 (55.56%)

3 (50.00%)

 > .999

Renal cysts (Kidney cysts)

47 (52.22%)

40 (50.00%)

7 (70.00%)

.320

Adrenal, pheochromocytoma

25 (27.47%)

22 (27.16%)

3 (30.00%)

 > .999

Pancreas, serous cystadenoma

28 (31.11%)

23 (28.4%)

5 (55.56%)

.130

Pancreas, NET

15 (16.67%)

13 (16.05%)

2 (22.22%)

.642

Median FU duration (years)

 Hemangioblastoma, brain

6.32 (3.16, 9.89)

6.80 (3.35, 10.58)

4.08 (2.29, 4.59)

.032

 Renal cell carcinoma

6.12 (2.61, 11.27)

6.18 (2.99, 11.33)

4.94 (1.24, 6.83)

.170

  1. NET Neuroendocrine tumor, FU Follow up