Table 1:

Analysis of clinical symptoms and outcomes of suprasellar papillary craniopharyngioma and suprasellar germ cell tumors

VariablesPCP (n = 18)GCT (n = 17)OR95% CIP Valuea
Age (yr)46 ± 13.9 (21–70)23 ± 7.1 (16–43)<.0001
Sex (male:female)13:513:41.3.27–5.7.7738
Symptoms
    Visual field deficits12 (67%)6 (35%).27.07–1.1.0634
    Hypopituitarismb12 (71%)12 (75%)1.3.27–5.8.7761
    Hyperprolactinemiac14 (93%)11 (67%).16.02–1.5.0834
    Hypothalamic dysfunction, including diabetes insipidus2 (11%)11 (65%)152.5–87.0010
Initial management.0303
    Total resection7 (39%)3 (18%)1.0
    Subtotal resection6 (33%)1 (6%).39.03–4.8
    Partial resection or biopsy3 (17%)6 (35%)4.7.67–32
    Radiation or radiosurgery2 (11%)7 (41%)8.21.03–65
Outcome
    Recurrenced13 (81%)4 (24%).10.02–.50.0031
    Survival (mean)39.6 ± 32.02 (2–118)52.4 ± 40.32 (13–123).3815
  • a P = statistical significance as calculated by the log-rank test.

  • b In the PCP group, n = 17; in the GCT group, n = 16.

  • c In the PCP group, n = 15; in the GCT group, n = 16.

  • d In the PCP group, n = 16; in the GCT group, n = 17.