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. Author manuscript; available in PMC: 2019 Oct 28.
Published in final edited form as: Mod Pathol. 2014 Sep 5;28(2):187–200. doi: 10.1038/modpathol.2014.109

TABLE 2:

Clinical Features of UCSF and WUSTL Case Cohorts

UCSF Cohort WUSTL Cohort
Malignant Peripheral Nerve Sheath Tumor Cellular Schwannoma p* Malignant Peripheral Nerve Sheath Tumor Cellular Schwannoma p* p**
Gender; Male (%) 17 (43%) 6 (50%) 0.75 33 (44%) 6 (43%) 0.83 0.55
Age, years^ 37.5 44.7 0.14 38.3 46 0.6 0.52
median (range) (11.2-71.8) (13.8-70.3) (0.1-81.6) (16-70)
<40 years old (%) 23 (58%) 5 (42%) 0.51 39 (52%) 6 (43%) 0.57 0.73
NF 1 (%) 25 (64%) 0 <0.0001 26 (72%) 1# (7%) <0.0001 0.31
NF 2 (%) 0 1 (8%) 0 1# (7%)
Size, cm^ 8.8 (0.5-26) 4.8 (1-9.8) 0.005
Site; Extremity (%) 12 (30%) 0 0.047 22 (31%) 3 (21%) 0.75 0.55

UCSF: University of California San Francisco; WUSTL: Washington University in St. Louis;

*:

p value belongs to comparisons between MPNSTs and CSs;

**:

p value belongs to comparisons between two institutions;

^:

Values are median (range);

#:

Type of Neurofibromatosis is unclear from medical records; NF: Neurofibromatosis; p values in bold are statistically significant.