Table 1.

EBV-associated B-cell LPDs

Infectious mononucleosis 
Posttransplant and other iatrogenic B-cell LPDs 
 Monomorphic, polymorphic, plasmacytic, or HL-like variants 
Lymphomatoid granulomatosis 
EBV+ DLBCL associated with chronic inflammation 
 Fibrin-associated DLBCL 
 Pyothorax-associated lymphoma 
EBV+ mucocutaneous ulcer 
Hodgkin’s lymphoma 
 Subset of classic and HIV-associated 
 Mainly mixed cellularity and lymphocyte depleted 
Primary effusion lymphoma (HHV-8 and EBV) 
Germinotropic B-LPD (HHV-8 and EBV) 
Plasmablastic lymphoma 
Primary CNS lymphoma 
 Immunocompromised patients (e.g. HIV) 
EBV+ DLBCL, NOS 
Burkitt lymphoma 
 All endemic and a subset of sporadic and HIV associated 
Infectious mononucleosis 
Posttransplant and other iatrogenic B-cell LPDs 
 Monomorphic, polymorphic, plasmacytic, or HL-like variants 
Lymphomatoid granulomatosis 
EBV+ DLBCL associated with chronic inflammation 
 Fibrin-associated DLBCL 
 Pyothorax-associated lymphoma 
EBV+ mucocutaneous ulcer 
Hodgkin’s lymphoma 
 Subset of classic and HIV-associated 
 Mainly mixed cellularity and lymphocyte depleted 
Primary effusion lymphoma (HHV-8 and EBV) 
Germinotropic B-LPD (HHV-8 and EBV) 
Plasmablastic lymphoma 
Primary CNS lymphoma 
 Immunocompromised patients (e.g. HIV) 
EBV+ DLBCL, NOS 
Burkitt lymphoma 
 All endemic and a subset of sporadic and HIV associated 

HL, Hodgkin lymphoma; HHV-8, human herpesvirus 8; NOS, not otherwise specified.

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