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. Author manuscript; available in PMC: 2012 Jan 1.
Published in final edited form as: Am J Med Genet A. 2011 Jan;155A(1):168–173. doi: 10.1002/ajmg.a.33760

TABLE II.

Pheo Parameters Compared Between VHL Type 2A Families

Family 1 Family 2 P value
Clinical parameters
 Age first pheo diagnosis (y) (n=30; 33) 28.8 19.7 0.02a
 Diagnosis by symptoms (n=52; 49) 42 (81%) 33 (67%) 0.17
 Secretion of Norepi only (n=30; 33) 19 (63%) 16 (49%) 0.31
 Secretion of VMA only (n=30; 33) 4 (13%) 0 0.05a
 Metachronous pheo (n=65; 65) 21 (32%) 13 (20%) 0.16
 Time to new occurrence (y) (n=21; 12) 7.8 12.8 0.08
Pathologic parameters
 Size (cm) (n=41; 33) 3.60 3.20 0.33
 Weight (g) (n=29; 18) 33.3 30.1 0.81
 R Laterality (n=63; 54) 20 (32%) 19 (35%) 0.84
 L Laterality (n=63; 54) 22 (35%) 17 (31%) 1.00
 Extra-adrenal (n=63; 54) 9 (14%) 15 (28%) 0.11
 Abdominal (n=9; 15) 7 (78%) 11 (73%) 1.00
Organ of zuckerkandl (n=7; 11) 2 (29%) 7 (64%) 0.33
 Chest (n=9; 15) 0 3 (20%) 0.27
 Neck (n=9; 15) 1 (11%) 0 0.37
 Synchronous (multifocal at presentation) (n=65; 55) 26 (40%) 33 (60%) 0.04a

Pheo, pheochromocytoma; Norepi, norepinephrine; VMA, vanillylmandelic acid; y, years.

Not all pheos were informative for each parameter, thus the specific n (Family 1; Family 2) is denoted under each category.

a

Statistical significance.