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. 2020 Sep 2;105(12):e4661–e4670. doi: 10.1210/clinem/dgaa608

Table 3.

Characteristics of 143 patients with pheochromocytoma/paraganglioma (PCC/PGL)

Characteristics Paraganglioma N = 37 Pheochromocytoma N = 106 P value
Mean age, years ± SD 45.1 ± 15.5 48.5 ± 15.3 .2516
Female sex, n (%) 22 (59.5) 67 (63.2) .0164
Race, n (%) .2955
 African American 10 (27.0) 25 (23.6)
 Caucasian 23 (62.2) 57 (53.8)
 Other 4 (10.8) 24 (22.6)
Germline susceptibility gene mutation, n (%) <.0001
 No mutation 12 (32.4) 41 (38.7)
 Not tested 7 (18.9) 43 (40.6)
NF1 0 (0) 9 (8.5)
RET 1 (2.7) 5 (4.7)
SDHB 11 (29.7) 0 (0)
SDHD 4 (10.8) 1 (0.9)
 Variant of undetermined significance 1 (2.7)a 1 (0.9)b
VHL 1 (2.7) 6 (5.7)
Dominant secreted catecholamine, n (%) .0373
 Epinephrine 6 (16.2) 36 (34.0)
 Norepinephrine 29 (78.4) 59 (55.7)
 Unknown 1 (2.7) 9 (8.5)
Median tumor size, cm (IQR) 4.5 (4.0, 5.8) 4.6 (3.2, 7.5) .4546
Median PASS score (IQR) 6.5 (4.0, 8.0)
Median GAPP score (IQR) N = 132 3.0 (3.0, 4.0) 3.0 (2.0, 4.0) .038

Bolded values indicate P ≤ 0.05.Abbreviations: SD, standard deviation; IQR, interquartile range; NF1, Neurofibromatosis 1; RET, Rearranged during transfection; SDHB, Succinate dehydrogenase subunit B; SDHD, Succinate dehydrogenase subunit D; VHL, von Hippel Lindau.

a SDHD c.T320C; p.L107P.

b TMEM127 c0.409 + 7C>T.