Use of an expanded immunohistochemical panel to distinguish cutaneous Hodgkin lymphoma from histopathologic imitators

J Cutan Pathol. 2012 Jun;39(6):651-8. doi: 10.1111/j.1600-0560.2012.01872.x. Epub 2012 Feb 11.

Abstract

In lymph nodes, classical Hodgkin lymphoma can typically be distinguished from non-Hodgkin lymphoma (NHL) by the presence of Hodgkin and Reed-Sternberg cells that co-express CD30 and CD15. However, anaplastic large cell lymphoma (ALCL) and diffuse large B-cell lymphoma (DLBCL) can show identical features, and some cases of classical Hodgkin lymphoma lack CD15 expression, rendering them difficult to differentiate from CD30-positive NHL. The differential diagnosis of cutaneous Hodgkin lymphoma similarly includes ALCL and DLBCL, and, additionally, tumors of mycosis fungoides. Recent studies have shown that classical Hodgkin lymphoma is of B-cell origin in virtually all cases, and shows at least focal weak expression of the B-cell marker PAX5 and often focal weak expression and no expression of the B-cell markers Oct-2 and BOB.1, respectively. All three of these markers are almost invariably absent in T-cell lymphomas and are strongly expressed in B-cell lymphomas. We report a 40-year-old man with classical Hodgkin lymphoma who developed cutaneous nodules. A biopsy from one revealed Hodgkin/Reed-Sternberg cells with a similar immunophenotype to the diagnostic lymph node biopsy, namely CD30+/CD15+, diffusely but weakly PAX5+, focally weakly Oct-2+ and lacking BOB.1 expression, thereby confirming a diagnosis of cutaneous Hodgkin lymphoma. To our knowledge, this is the first report of the expression pattern of the combination of PAX5, Oct-2 and BOB.1 in the context of cutaneous involvement by Hodgkin lymphoma.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • B-Lymphocytes / metabolism
  • B-Lymphocytes / pathology
  • Biomarkers, Tumor / metabolism*
  • Biopsy
  • Diagnosis, Differential
  • Hodgkin Disease* / metabolism
  • Hodgkin Disease* / pathology
  • Humans
  • Immunohistochemistry / methods
  • Octamer Transcription Factor-2 / metabolism*
  • PAX5 Transcription Factor / metabolism*
  • Reed-Sternberg Cells / metabolism
  • Reed-Sternberg Cells / pathology
  • Skin Neoplasms* / metabolism
  • Skin Neoplasms* / pathology
  • Trans-Activators / metabolism*

Substances

  • Biomarkers, Tumor
  • Octamer Transcription Factor-2
  • PAX5 Transcription Factor
  • PAX5 protein, human
  • POU2AF1 protein, human
  • Trans-Activators