BOB.1, CD79a and cyclin E are the most appropriate markers to discriminate classical Hodgkin's lymphoma from primary

Sylvia Hoeller1, Deborah Zihler, Inti Zlobec

  • 1Department of Pathology, University of Basel, Basel, Switzerland.

Histopathology
|January 28, 2010
PubMed

Insights

Distinguishing classical Hodgkin's lymphoma (cHL) from primary mediastinal B-cell lymphoma (PMBCL) can be challenging. Cyclin E, CD79a, and BOB.1 are accurate immunohistochemical markers for differentiating these lymphomas.

Area of Science:

  • Hematopathology
  • Immunohistochemistry
  • Lymphoma diagnostics

Background:

  • Classical Hodgkin's lymphoma (cHL) and primary mediastinal B-cell lymphoma (PMBCL) are distinct B-cell lymphomas.
  • Accurate differentiation is crucial for appropriate treatment selection.
  • Unclassified B-cell lymphomas with intermediate features pose diagnostic challenges.

Purpose of the Study:

  • To identify reliable immunohistochemical markers for distinguishing cHL from PMBCL.
  • To refine the definition of 'B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and cHL'.

Main Methods:

  • Analysis of 283 cHL and 51 PMBCL cases using tissue microarrays.
  • Evaluation of antibodies against BOB.1, CD15, CD20, CD23, CD30, CD79a, cyclin E, LMP-1, MUM1p, p63, and Oct2.
  • Calculation of marker cut-off scores using receiver-operating characteristic curves.

Main Results:

  • For cHL, markers with the highest positive predictive value were CD15, cyclin E, and LMP-1 (100%).
  • CD30 (92%) and cyclin E (79%) showed high sensitivity for cHL, but CD30 had lower specificity (81%) due to PMBCL positivity.
  • For PMBCL, CD23 (98%), p63 (96%), BOB.1 (94%), and CD79a (90%) demonstrated high positive predictive values, with BOB.1 (100%) and CD79a (89%) showing high sensitivity.

Conclusions:

  • The combination of cyclin E, CD79a, and BOB.1 demonstrates high accuracy in differentiating cHL and PMBCL.
  • These markers can aid in the differential diagnosis of challenging lymphoma cases.
  • Refined diagnostic criteria improve classification of B-cell lymphomas.
Abstract

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