Table 1.

Cytotoxic Granule Protein Expression in ALCL, HD, and LBCL

CasesTIA-1PerforinOverall Positivity (%)
(%)(%)
ALCL 23/33 (70) 22/33 (67) 25/33 (76) 
Classical systemic 13/19 (68) 14/19 (74) 15/19 (79) 
Histiocyte rich variant 6/6 (100) 6/6 (100) 6/6 (100) 
Small cell variant 2/2 (100) 2/2 (100) 2/2 (100) 
Primary cutaneous 0/3 0/3 0/3 
AIDS-associated 2/3 (67) 0/3 2/3 (67) 
 
HD 5/51 (10) 0/26 5/51 (10) 
LP HD 0/3 0/1 0/3 
NS HD 2/33 (6) 0/18 2/33 (6) 
MC HD 2/11 (18) 0/5 2/11 (18) 
LD HD 1/4 (25) 0/2 1/4 (25) 
 
LBCL 0/17 (0) 0/12 (0) 0/17 (0) 
Diffuse LBCL 0/10 0/8 0/10 
T-cell rich BCL 0/3 0/1 0/3 
Mediastinal LBCL 0/2 0/1 0/2 
Follicular LBCL 0/1 0/1 0/1 
LBCL with LP HD 0/1 0/1 0/1 
CasesTIA-1PerforinOverall Positivity (%)
(%)(%)
ALCL 23/33 (70) 22/33 (67) 25/33 (76) 
Classical systemic 13/19 (68) 14/19 (74) 15/19 (79) 
Histiocyte rich variant 6/6 (100) 6/6 (100) 6/6 (100) 
Small cell variant 2/2 (100) 2/2 (100) 2/2 (100) 
Primary cutaneous 0/3 0/3 0/3 
AIDS-associated 2/3 (67) 0/3 2/3 (67) 
 
HD 5/51 (10) 0/26 5/51 (10) 
LP HD 0/3 0/1 0/3 
NS HD 2/33 (6) 0/18 2/33 (6) 
MC HD 2/11 (18) 0/5 2/11 (18) 
LD HD 1/4 (25) 0/2 1/4 (25) 
 
LBCL 0/17 (0) 0/12 (0) 0/17 (0) 
Diffuse LBCL 0/10 0/8 0/10 
T-cell rich BCL 0/3 0/1 0/3 
Mediastinal LBCL 0/2 0/1 0/2 
Follicular LBCL 0/1 0/1 0/1 
LBCL with LP HD 0/1 0/1 0/1 

Abbreviations: LD, lymphocyte depletion; LP, nodular lymphocyte predominance; MC, mixed cellularity; NS; nodular sclerosis.

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