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. Author manuscript; available in PMC: 2012 May 8.
Published in final edited form as: Mod Pathol. 2009 May 1;22(7):950–958. doi: 10.1038/modpathol.2009.52

Table 1.

Associations between levels of CAFs, Schwannian Stroma, MVP and clinical risk factors in the CMH cohort

Characteristic CAFs Low CAFs High Total P

Diagnosis <0.001
NB(A+B+C) 9 (21%) 33 (78%) 42
A. Undifferentiated NB 1 (20%) 4 (80%) 5
B. Poorly differentiated NB 2 (14%) 12 (86%) 14
C. Differentiating NB 6 (26%) 17 (74%) 23
Nodular GNB 0 (0%) 4 (100%) 4
Intermixed GNB 5 (71%) 2 (29%) 7
GNR 7 (100%) 0 (0%) 7

Schwannian Stroma <0.001
NB+nodular GNB, SS-poor 9 (20%) 37 (80%) 46
Intermixed GNB+GNR, SS-rich 12 (86%) 2 (14%) 14

Microvascular Proliferation <0.001
NB+intermixed GNB+GNR, no MVP 13 (60%) 9 (40%) 22
NB and nodular GNB with MVP 5 (16%) 33 (84%) 38

Age * 0.51
< 12 months 4 (21%) 15 (79%) 19
≥ 12 months 10 (29%) 24 (71%) 34

Risk Group * 0.88
High-Risk 3 (20%) 12 (80%) 15
Non High-Risk 7 (28%) 18 (72%) 25

MYCN * 0.75
Amplified 2 (22%) 7 (78%) 9
Non-amplified 11 (28%) 29 (72%) 40

Histology * 0.18
Unfavorable 3 (13%) 20 (86%) 23
Favorable 8 (29%) 20 (71%) 28

Stage * 0.49
1, 2, 3 , 4S 10 (29%) 24 (70%) 34
4 3 (20%) 12 (80%) 15

Survival * 0.89
Dead 2 (29%) 5 (71%) 7
Alive 12 (26%) 34 (74%) 46

NB: neuroblastoma; GNB: ganglioneuroblastoma; GNR:ganglioneuroma; SS: Schwannian Stroma

*

only NB+GNB