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. 2015 Jul 15;10(7):e0131635. doi: 10.1371/journal.pone.0131635

Table 1. Main characteristics of the 27 patients with LCH divided in two groups according to the presence of either MRI alterations specific for ND-LCH (Group 1) or only of risk factors for ND-LCH (Group 2).

Group 1N = 17 Group 2N = 10 Difference(95% confidence interval)p-value
Gender 9 M, 8 F 7 M, 3 F
Median age at study entry (range) 8.2 years(1.7 to 27.5 years;quartiles: 5, 8.2, 11.7 years) 10.2 years(3.7 to 16.4 yearsquartiles: 5.8, 10.2, 14.8 years) -2.02 years(-8.97;4.6)p = 0.688
Median time between the onset of LCH and the first MRI evaluation 4.2 years 2.4 years 1.8 years(-1.3;5.1)p = 0.248
Median time between the l onset of LCH and the first observation of ND-LCH at MRI 4.2 years(quartiles: 0.8; 2.5; 4.2; 6.5; 14.5 years). n.a.
Median age at onset s of LCH 2 years(range, 4 months -18 years;quartiles: 0.9, 2 and 3.3 years) 5.5 years(range, 18 months -15 years; quartiles: 3.2, 5.5 and 9.5 years) -3.years(-8.4;-0.7)p = 0.024
Multisystem vs. Single system 13 (76%) vs. 4 6 (60%) vs. 4 16%(-20;53%)p = 0.365
Reactivating or chronic active LCH 15 (88%) 6 (60%) 28%(6;62%)p = 0.088
Risk lesions for ND-LCH: Diabetes insipidus / Craniofacial lesions 11 / 6 6 / 5* Odds Ratio 1.53(0.32; 7.37)p = 0.591
Previous chemotherapy ongoing 15 (88%)7 (41%) 9(90%)4(40%) -2%(-26; 22%)p = 0.888/1%(-37; 39%)p = 0.952

This is the Table 1 footnote.

* one patient had both risk factors