Clinically, primary cutaneous
diffuse large cell lymphoma, leg type, is aggressive with a 5-year overall survival of 41%.
These lymphomas are characterized by a predominantly periportal infiltration of large lymphoid cells of the B-cell phenotype,[8] although they may rarely express a T-cell phenotype.[5]
Diffuse large cell lymphoma is the most common subtype of non-Hodgkin lymphoma (46%).
The combination of 2 different types of NHL composed of small cleaved cell lymphoma and
diffuse large cell lymphoma is the most common variant, accounting for up to 58% of cases.[3] Composite lymphomas, composed of HD and one of the components of NHL, are very rare.
Diffuse large cell lymphomas: identification of prognostic factors and validation of the International Non Hodgkin's Lymphoma Prognostic Index.
(33.) Grogan TM, Lippman SM, Spier CM, Slymen DJ, Rybski JA, Rangel CS, Richter LC, Miller TP Independent prognostic significance of a nuclear proliferation antigen in
diffuse large cell lymphomas as determined by the monoclonal antibody Ki-67.
(1) Many recent studies have used immunophenotypic markers to subclassify
diffuse large cell lymphomas into prognostic groups or groups with similar behavior.
Follicular lymphomas and
diffuse large cell lymphomas represent the most common subtypes of primary lymphoma in the cervix and are usually classified as Ann Arbor stage I or II.