“…We analyzed 133 patients with HL aged 13 ± SEM 0.32 (range 3 to 18) years, treated according to the AIEOP LH-2004 between 2004 and 2017 [1] The inclusion criteria required biological samples for genetic analysis of HLA-G SNP, a set of hematological and biochemical parameters (i.e., erythrocyte sedimentation rate, albumin, ferritin, hemoglobin, white blood cell (WBC) count, neutrophils, eosinophils, basophils, lymphocytes, monocytes, and platelets); TG groups; World Health Organization (WHO) histological classification of HL (i.e., HD of unclassifiable subtype; MC, mixed cellularity; LRCHL, lymphocyte-rich cHL; NS, nodular sclerosis); sex; and age. Compared with our previous report on HLA-G SNP [4], the present study concerns a median followup about three years longer (median 5.55 years (interquartile range (IQR) 4.09-7.93)), 66 new cases, and hematological and biochemical parameters.…”