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2 iatric cases (two lymphocyte-predominant, 25 nodular sclerosis, 16 mixed cellularity, 5 lymphocyte de
3 -rich (81-fold; 95% CI, 30- to 177-fold) and nodular sclerosis (4.6-fold; 95% CI, 2.9- to 7.0-fold) a
4 RS cells expressed BCL-2 in 359 (65%) of 551 nodular sclerosis, 67 (47%) of 143 mixed cellularity, an
5 vealed that the majority of the patients had nodular sclerosis (80.7%) and were classified as stage I
6 rall, 6 (3 T and 3 null) of 49 ALCL and 3 (2 nodular sclerosis and 1 mixed cellularity) of 72 HD show
8 These associations were significant for the nodular sclerosis and mixed cellularity subtypes but wer
13 phocyte-rich/mixed cell/lymphocyte depleted, nodular sclerosis, classical HL, not otherwise specified
16 thyroidism (thyroid radiation dose, sex, and nodular sclerosis histology), the risk of hypothyroidism
17 logical subtypes (odds ratio [OR] for MC vs. nodular sclerosis histology, 3.2; 95% confidence interva
19 loci within the HLA region are observed for nodular sclerosis Hodgkin lymphoma (rs9269081, HLA-DPB1*
20 th Reed-Sternberg cells in 30 of 35 cases of nodular-sclerosis, lymphocyte-depletion, and mixed-cellu
21 on into one of the four types of classic HL (nodular sclerosis, mixed cellularity, lymphocyte-deplete
23 pecific mortality but only for patients with nodular sclerosis (NS) histologic subtype (hazard ratio
24 low stage (stage I/II) at presentation with nodular sclerosis (NS) histology predominating in 80% of
26 B2M-deficient cases encompassed most of the nodular sclerosis subtype cases and only a minority of m
27 ologic features, it clinically resembles the nodular sclerosis subtype of classical Hodgkin lymphoma
29 wo of three lymphocyte-predominant, 26 of 39 nodular, sclerosis, two of two mixed cellularity, and tw
30 ssumed dendritic shapes, particularly in the nodular sclerosis type, producing an interdigitating mes