Lymphocyte Depleted Classical Hodgkin Lymphoma (LDCHL)

Less than 1% of cases of classical Hodgkin lymphoma (CHL) fall into this category.  This variant is manifested by numerous Hodgkin’s/ Reed-Sternberg cells without a significant reactive inflammatory infiltrate.  These cases can easily be mistaken for other types of malignancy or anapestic large cell lymphoma.  Immunophenotyping is critical.  EBV infection is present in >90% of cases,  And is more common in HIV-positive individuals, older adults, and third world countries.  Co-expression of CD30 and PAX-5 is helpful to differentiate from a aplastic large cell lymphoma (ALCL).
Classical Hodgkin Lymphoma – General Information
 
Characteristic Immunohistochemical Features

References
Hematopathology. [edited by] Jaffe, ES. 1st. ed. Elsevier, Inc. © 2011.
 
Robbins and Cotran Pathologic Basis of Disease.  V Kumar, et al. 9th Edition. Elsevier Saunders. 2015.
 
WHO Classification of Tumors of Haematopoietic and Lymphoid Tissues.  SH Swerdlow, et al. International Agency for Research on Cancer. Lyon, 2008.