Table 1.
Clinicopathological characteristics and mutation status
sample | tumor | location | family history | mutation | sex | age at onset (yrs) | multiple paragangliomas |
1 | PGL04 | CBT | PGL2 | - | f | 28 | yes |
2 | PGL01 | CBT | PGL2 | - | f | 28 | yes |
3 | PGL02 | CBT | PGL2 | - | m | 37 | yes |
4 | PGL19 | CBT | PGL2 | - | f | 32 | yes |
5 | PGL05 | CBT | SDHD | D92Y | m | 43 | yes |
6 | PGL06 | CBT | SDHD | D92Y | m | 47 | yes |
7 | PGL13 | CBT | SDHD | D92Y | f | 29 | yes |
8 | PGL14 | CBT | SDHD | D92Y | f | 45 | no |
9 | PGL16 | CBT | SDHD | D92Y | f | 47 | yes |
10 | PGL17 | CBT | SDHD | D92Y | f | 74 | no |
11 | PGL10 | CBT | SPOR | - | f | 44 | no |
13 | PGL12 | CBT | SPOR | - | f | 49 | no |
14 | PGL15 | CBT | SPOR | - | f | 38 | no |
15 | PGL23 | CBT | SPOR | - | f | 70 | no |
16 | PGL20 | CBT | SPOR | - | m | 27 | no |
CBT = carotid body tumor; PGL2 = positive family history for PGL2-linked paragangliomas; SDHD = positive family history for SDHD-linked paragangliomas; SPOR = sporadic sample, negative family history of paraganglioma or phaeochromocytoma and no mutation in the SDHB, SDHC or SDHD gene; D92Y = Asp92Tyr, a Dutch founder mutation in the SDHD gene; m = male patient, f = female patient.