| Literature DB >> 24019247 |
Lucie M Turcotte1, Colleen K Correll, Robyn C Reed, Christopher L Moertel.
Abstract
Castleman disease is a rare lymphoproliferative disorder, which presents in a unicentric or multicentric fashion. Multicentric Castleman disease (MCD) is associated with significant systemic symptoms, in part related to the underlying role of interleukin-6 in disease pathogenesis. Treatment for MCD has not been well established and prognosis has historically been poor. We present a case of severe MCD in a pediatric patient who has shown sustained remission following multi-agent chemotherapy and targeted maintenance therapy with the interleukin-6 receptor inhibitor, tocilizumab. This represents the first case report of sustained remission of MCD in a pediatric patient following discontinuation of tocilizumab therapy.Entities:
Keywords: CHOP; anakinra; multicentric Castleman disease; tocilizumab
Mesh:
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Year: 2013 PMID: 24019247 PMCID: PMC3946294 DOI: 10.1002/pbc.24761
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167