Comparison of histologic nodal reactive patterns, cell suspension immunophenotypic data, and HIV status

C D Westermann1, P E Hurtubise, C C Linnemann

  • 1Department of Pathology and Laboratory Medicine, University of Cincinnati College of Medicine, Ohio.

Insights

Immunophenotypic analysis of reactive lymphoid hyperplasia reveals distinct cell profiles. Findings correlate with specific hyperplasia types and HIV status, aiding in understanding non-malignant lymph node changes.

Area of Science:

  • Hematology
  • Immunology
  • Pathology

Background:

  • Cell suspension immunophenotyping is crucial for diagnosing lymphoid malignancies.
  • Interpretation of immunophenotypic data in reactive lymphoid proliferations is less understood.
  • Reactive lymphoid hyperplasia encompasses various non-malignant lymph node conditions.

Purpose of the Study:

  • To analyze cell suspension immunophenotypic findings in reactive lymphoid proliferations.
  • To correlate these findings with specific histologic categories of hyperplasia.
  • To investigate the influence of human immunodeficiency virus (HIV) status on these profiles.

Main Methods:

  • Analysis of immunophenotypic data from 119 lymph nodes with reactive lymphoid proliferations.
  • Categorization into follicular hyperplasia (marked/moderate), dermatopathic lymphadenopathy, and diffuse hyperplasia.
  • Computer-assisted morphometry to assess follicle characteristics; HIV status analyzed in 57 cases.

Main Results:

  • Dermatopathic lymphadenopathy showed higher CD3+ T cells, elevated CD4:CD8 ratios, and fewer CD19+ B cells.
  • Marked follicular hyperplasia exhibited lower CD4:CD8 ratios, with increased CD19+, CD10+, and transferrin receptor-positive cells.
  • HIV-negative cases had higher nodal CD4:CD8 ratios than HIV-positive cases; peripheral blood ratios correlated strongly.

Conclusions:

  • Distinct immunophenotypic profiles are associated with specific types of reactive lymphoid hyperplasia.
  • Morphometric data support correlations between follicular hyperplasia and specific cell populations.
  • While variations exist, these findings aid in differentiating reactive changes from lymphoid malignancies.

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