Table 1.
Parameter | Metastatic pheochromocytoma (n=41) |
Benign pheochromocytoma (n=108) |
P |
---|---|---|---|
Gender (male/female) | 19/22 | 44/62 | NS |
Age (years) (min; max) | 41.4±14.7 (6;83) | 50.2±13.7 (21;78) | <0.001 |
Age <40 years (%) | 19 (46.3%) | 26 (24.1%) | 0.008 |
Tumor dimension (cm) (min; max) | 8.38±3.27 (2.4;17) | 6.18±2.75 (2;16) | <0.001 |
Number of tumors ≥5cm | 37 (90%) | 72 (66.7%) | 0.002 |
Right adrenal | 28 (68.3%) | 59 (54.6%) | 0.11 |
Left adrenal | 12 (29.3%) | 44 (40.7%) | NS |
Bilateral adrenal involvement | 4 (9.8%) | 5 (4.6%) | NS |
Syndromic presentation | 9 (25.7%) | 11 (14.7%) | 0.13 |
SDHB | 2 | 0 | |
MEN 2 | 4 | 2 | |
VHL | 3 | 5 | |
NF1 | 0 | 4 |
SDHB, succinate dehydrogenase subunit B; MEN 2, multiple endocrine neoplasia type 2; VHL, von Hippel-Lindau; NF1, neurofibromatosis type 1; NS, non-significant.