[Stroma-rich variant of hyaline-vascular Castleman's disease: a clinicopathologic and histogenetic study]

Yan Xiong1, Ying Zhang, Ying Wang

  • 1Department of Pathology, Peking University First Hospital, Beijing, China.

Insights

Hyaline-vascular Castleman's disease (HVCD) shows distinct variants, with stromal cell proliferation correlating significantly with paraneoplastic pemphigus. Interfollicular stromal cells in HVCD are primarily fibroblastic reticular cells expressing CCL21 and MSA.

Area of Science:

  • Hematopathology
  • Immunohistochemistry
  • Lymphoproliferative Disorders

Background:

  • Hyaline-vascular Castleman's disease (HVCD) is a lymphoproliferative disorder with distinct clinicopathologic features.
  • Interfollicular stromal cells play a role in lymph node microenvironment and disease pathogenesis.

Purpose of the Study:

  • To investigate the histologic and immunohistochemical characteristics of interfollicular stromal cells in HVCD.
  • To explore the association between stromal cell features and paraneoplastic pemphigus in HVCD.

Main Methods:

  • Review of 23 HVCD cases, including stroma-rich and conventional variants.
  • Immunohistochemical analysis for CCL21, MSA, CD21, CD35, S-100, and CD34 on stromal cells.

Main Results:

  • Stroma-rich HVCD, characterized by prominent interfollicular areas, was associated with paraneoplastic pemphigus (P < 0.01).
  • Stromal cells in both HVCD variants were positive for CCL21 and MSA, but negative for CD21, CD35, S-100, and CD34.
  • Stromal cell hyperplasia showed a statistically significant correlation with paraneoplastic pemphigus.

Conclusions:

  • Stroma-rich and conventional HVCD are distinct histologic variants with differing associations with paraneoplastic pemphigus.
  • Interfollicular stromal cells in HVCD are likely fibroblastic reticular cells with a CCL21(+)/MSA(+)/CD34⁻/CD21⁻/S-100⁻ immunophenotype.
  • Stromal cell proliferation is linked to paraneoplastic pemphigus, warranting further investigation into the underlying pathogenesis.
Abstract

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