| Literature DB >> 20122250 |
Iris A C de Vries1, Marjolein M S van Acht, Thomas B J Demeyere, Marnix L M Lybeert, Jean-Paul de Zoete, Grard A P Nieuwenhuijzen.
Abstract
BACKGROUND: Castleman disease (CD) is a rare benign disorder characterised by hyperplasia of lymphoid tissue that may develop at a single site or throughout the body. The etiology of this disorder is unclear, although the histopathological presentation can be differentiated into a hyaline vascular variant, a plasma cell variant and a mixed variant. Clinically, it has been recorded that 3 manifestations of CD are characterized: a localized unicentric type, a generalized multicentric type and a mixed form. Surgery remains the main treatment for resectable unicentric CD, since removal of the large node is possible without further complications. No consensus has been reached concerning the most adequate treatment for irresectable unicentric CD.Entities:
Mesh:
Year: 2010 PMID: 20122250 PMCID: PMC2827478 DOI: 10.1186/1748-717X-5-7
Source DB: PubMed Journal: Radiat Oncol ISSN: 1748-717X Impact factor: 3.481