Castleman disease, TAFRO syndrome, idiopathic plasmacytic lymphadenopathy, and autoimmune disease
Author:
Affiliation:
1. Department of Pathology, Tokai University School of Medicine, Kanagawa, Japan
Publisher
Japanese Society for Lymphoreticular Tissue Research
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jslrt/62/2/62_22016/_pdf
Reference14 articles.
1. 1 Castleman B, Towne VW. Case 40011. N Engl J Med. 1954; 250: 26-30.
2. 2 Frizzera G, Banks PM, Massarelli G, Rosai J. A systemic lymphoproliferative disorder with morphologic features of Castleman’s disease. Pathological findings in 15 patients. Am J Surg Pathol. 1983; 7: 211-231.
3. 3 Fajgenbaum DC, Uldrick TS, Bagg A et al. International, evidence-based consensus diagnostic criteria for HHV-8–negative/idiopathic multicentric Castleman disease. Blood. 2017; 129: 1646-1657.
4. 4 Mori S et al. J Jpn. Soc Res (New York). 1980; 20(suppl): 55-65 [in Japanese].
5. 5 Kojima M, Nakamura N, Tsukamoto N et al. Clinical implications of idiopathic multicentric castleman disease among Japanese: a report of 28 cases. Int J Surg Pathol. 2008; 16: 391-398.
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