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[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.
Objective:
To study the histologic features and immunohistochemical findings of interfollicular stromal cells in hyaline-vascular Castleman's disease (HVCD), and to explore the role of these stromal cells in the pathogenesis of this disease.
Methods:
The clinical findings and microscopic features of 23 cases of HVCD cases were reviewed. Immunohistochemical study for CCL21, MSA, CD21, CD35, S-100 and CD34 was carried out.
Results:
According to the criteria proposed by Danon et al., stroma-rich variant of HVCD contained prominent interfollicular zone which occupied at least 50% of the lymph node area. In the current study, there were 14 cases of stroma-rich HVCD and 9 cases of conventional HVCD. Eleven of the stroma-rich HVCD had paraneoplastic pemphigus and contrastly, no pemphigus lesion obtained in all the 9 cases of conventional HVCD. The association between stromal cell hyperplasia and paraneoplastic pemphigus was statistically significant (P < 0.01).In all the conventional HVCD cases studied, CCL21 and MSA were positive in the stromal cells.The stromal cells in 13 of the 14 cases of the stroma-rich HVCD were also positive for CCL21 and MSA, however, staining for CD21, CD35, S-100 and CD34 was negative in both groups. There was no statistical significance obtained (P > 0.05) between the differences of the staining results.
Conclusions:
Stroma-rich HVCD and conventional HVCD represent two distinctive histologic variants and have a different association with paraneoplastic pemphigus. Most of the stromal cells locating in the interfollicular areas are fibroblastic reticular cells in origin, with the immunophenotype as CCL21(+)/MSA(+)/CD34⁻/CD21⁻/S-100⁻. The stromal cells proliferation correlate with the occurrence of paraneoplastic pemphigus, nevertheless, more cases are expected for a further study of the underlying pathogenesis.
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