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. 2024 Jan 28;64(1):1–9. doi: 10.3960/jslrt.23038

Table 1. Demographics and clinical findings for MTX-LPD.

MTX-LPD (n = 48)
DLBCL type (n = 24) CHL type (n = 24) P
Age, mean (range) 76.1 (62–87) 66.8 (41–82) 0.002*
Sex (male:female) 3:21 8:16 0.084
Underlying condition n (%)
Rheumatoid arthritis 21 (87.5) 20 (83.3)
Hashimoto disease 1 (4.2) 0
SAPHO syndrome 0 1 (4.2)
Crohn disease 0 1 (4.2)
Unknown 3 (12.5) 2 (8.3)
Excised or biopsied site n (%)
Lymph nodes 15 (62.5) 23 (95.8)
Axillary 6 (25.0) 3 (12.5)
Cervical 4 (16.7) 8 (33.3)
Subclavicular 0 3 (12.5)
Mediastinal 0 1 (4.2)
Inguinal 3 (12.5) 4 (16.7)
Peribronchial 1 (4.2) 0
Retroperitoneum 0 3 (12.5)
LN of unknown site 1 (4.2) 1 (4.2)
Soft tissue 2 (8.3) 0
Skin 2 (8.3) 0
Stomach 2 (8.3) 0
Tonsil 1 (4.2) 0
Gingiva 1 (4.2) 0
Orbit 1 (4.2) 0
Liver 0 1 (4.2)
Presence of EBV infection
Present 15 (62.5) 22 (91.7) 0.011*
Absent 8 (33.3) 1 (4.2)

†The presence of EBV infection was evaluated by EBER in situ hybridization or LMP-1 immunostaining in proliferating atypical lymphocytes, and 23 cases each of DLBCL type and CHL type were evaluated. Significance was calculated using the Mann–Whitney U test. Fisher’s exact analysis was used for the statistical analysis of nominal scales. *P < 0.05.