Reactivation of Behçet's disease in the course of multicentric HHV8‐positive Castleman's disease: long‐term complete remission by a combined chemo/radiation and interferon‐α therapy regimen
Open Access
- 1 December 1998
- journal article
- case report
- Published by Wiley in British Journal of Haematology
- Vol. 103 (3) , 788-790
- https://doi.org/10.1046/j.1365-2141.1998.01038.x
Abstract
We used a new combined chemo‐ (COP/ABVD), radiation and interferon‐α (10 × 106 IU s.c. 3× per week/12 months) therapy regimen to treat severe multicentric Castleman's disease (CD) complicated by relapsing Behçet's disease (BD) manifestations. More than 16 years after diagnosis of CD the patient remains in very good clinical condition, with remission of all CD and BD manifestations 13 months after discontinuation of the interferon‐α treatment. In addition, our clinicopathological, immunohistological and virological data suggest a pathogenetic link between CD and BD via activation of pre‐existing BD‐specific plasma cells due to CD‐related HHV8‐induced overexpression of interleukin‐6.Keywords
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