Are multicentric Castleman's disease with cutaneous plasmacytosis and systemic plasmacytosis the same entity?
Author:
Publisher
Wiley
Subject
General Medicine,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2559.2006.02532.x/fullpdf
Reference12 articles.
1. Angiofollicular and plasmacytic polyadenopathy: a pseudotumourous syndrome with dysimmunity.
2. A systemic lymphoproliferative disorder with morphologic features of Castleman's disease: clinical findings and clinicopathologic correlations in 15 patients.
3. Skin involvement in giant lymph node hyperplasia (Castleman’s disease)
4. Systemic plasmacytosis. A syndrome of peculiar multiple skin eruptions, generalized lymphadenopathy, and polyclonal hypergammaglobulinemia
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1. Peripheral helper-T-cell-derived CXCL13 is a crucial pathogenic factor in idiopathic multicentric Castleman disease;Nature Communications;2023-10-31
2. Cutaneous reactive B‐cell lymphoid proliferations;Journal of Cutaneous Pathology;2022-08-04
3. Cutaneous Plasmacytosis and Idiopathic Multicentric Castleman Disease;The American Journal of Dermatopathology;2021-12-28
4. Skin‐associated lymphoid tissue could be a sign of systemic disease;British Journal of Dermatology;2021-04-06
5. Cutaneous involvement as initial presentation of multicentric plasmacytic Castleman disease;Journal of Cutaneous Pathology;2021-03-07
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