American Journal of Clinical Pathology · 2003 · 119 citations · 48 references
MedicineHematologyPathologyCellular PathologyMolecular OncologyMolecular PathologyB Cell BiologyLymphoid NeoplasmsLymphoid Tissue PathologyLymphoid TumorsDifferential Diagnosis CriteriaImmunohistochemical DetectionImmunohistochemical MarkersImmunohistochemical StainingLymphoma ClassificationLymphoma HistopathologyLymphoma Molecular Classification
Even with routine immunohistochemical evaluation, distinguishing classic Hodgkin lymphoma (CHL) from diffuse large B-cell lymphoma (DLBCL) or anaplastic large cell lymphoma (ALCL) can be difficult. In these cases, the transcription factors (B cell-specific activator protein [BSAP], octamer-binding transcription factor 2 [Oct-2], and B-cell Oct-binding protein 1 [BOB.1]) and the pan-B-cell markers (CD20, CD22, and CD79a) may aid in clarifying the diagnosis. In 57 cases of CHL, 5 cases of nodular lymphocyte predominant Hodgkin lymphoma (NLPHL), and 33 cases of non-Hodgkin lymphoma (25 DLBCL and 8 ALCL) we found the transcription factor phenotype BSAP+ and either Oct-2- or BOB.1- to be predictive of CHL; BSAP+/Oct-2+/BOB.1+ was predictive of NLPHL or DLBCL, while BSAP- was predictive of ALCL. Expression of all 3 pan-B-cell markers was seen only in NLPHL and DLBCL; positivity for a single B-cell marker was present only in CHL. Thus, together, the transcription factors and pan-B-cell markers might be useful in the differential diagnosis of CHL.
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World Health Organization Classification of Tumours
CDM Fletcher, Anke van den Berg, Ineke Molenaar · 2002 · 7.1K citations
Pathology and genetics: Tumours of haematopoietic and lymphoid tissues
Paresh Vyas · The Lancet Oncology · 2001 · 988 citations
Holger Kanzler, Ralf Küppers, Martin‐Leo Hansmann et al. · The Journal of Experimental Medicine · 1996 · 757 citations · Full text