Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2005-3-14
pubmed:abstractText
Benjamin Castleman first described multicentric Castleman's disease (MCD) in a series of cases in 1954. Interest in MCD has grown in recent years following an association with human immunodeficiency virus (HIV) infection. Castleman's disease is separated into localized disease and MCD. The latter is characterized by polylymphadenopathy and multiorgan involvement. Histologically, Castleman's disease is divided into the hyalinized vascular form and a plasma cell variant, the former being more common in localized disease and the latter more common in MCD. MCD is associated with Kaposi's sarcoma herpesvirus (KSHV) infection, which is alternatively termed human herpesvirus 8 (HHV8). This virus encodes a homologue of interleukin 6 (vIL 6), which may mediate some systemic features of MCD. The diagnosis of Castleman's disease is established by biopsy and treatment is often based on published case reports only, as there are no randomized trials of therapy. Surgery has less of a role in MCD than in localized disease, but debulking by splenectomy may be useful to alleviate haematological sequelae. Systemic treatments for MCD have included chemotherapy, anti-herpesvirus treatments to reduce the KSHV viral load, highly active antiretroviral therapy (HAART) to reduce HIV viraemia and latterly monoclonal antibodies against both IL 6 and CD20. The introduction of HAART has altered the natural history of HIV infection; however, its impact on MCD is difficult to ascertain. Optimization and consensus in treatment of these patients remains a target for the future.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0284-186X
pubmed:author
pubmed:issnType
Print
pubmed:volume
43
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
698-704
pubmed:dateRevised
2009-5-12
pubmed:meshHeading
pubmed-meshheading:15764213-Aged, pubmed-meshheading:15764213-Animals, pubmed-meshheading:15764213-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:15764213-Antiretroviral Therapy, Highly Active, pubmed-meshheading:15764213-Combined Modality Therapy, pubmed-meshheading:15764213-Female, pubmed-meshheading:15764213-Giant Lymph Node Hyperplasia, pubmed-meshheading:15764213-Herpesvirus 8, Human, pubmed-meshheading:15764213-Humans, pubmed-meshheading:15764213-Immunohistochemistry, pubmed-meshheading:15764213-Interleukin-6, pubmed-meshheading:15764213-Male, pubmed-meshheading:15764213-Mice, pubmed-meshheading:15764213-Middle Aged, pubmed-meshheading:15764213-Prognosis, pubmed-meshheading:15764213-Risk Assessment, pubmed-meshheading:15764213-Sarcoma, Kaposi, pubmed-meshheading:15764213-Severity of Illness Index, pubmed-meshheading:15764213-Viral Load
pubmed:year
2004
pubmed:articleTitle
Fifty years of multicentric Castleman's disease.
pubmed:affiliation
Department of Oncology The Chelsea and Westminster Hospital London UK.
pubmed:publicationType
Journal Article, Review