๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Multicentric Castleman's disease treated with antivirals and immunosuppressants

โœ Scribed by Sanjaya Senanayake; John Kelly; Andrew Lloyd; Zubair Waliuzzaman; David Goldstein; William Rawlinson


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
70 KB
Volume
71
Category
Article
ISSN
0146-6615

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

A patient negative for human immunodeficiency virus (HIV) developed multicentric Castleman's disease (MCD) and Kaposi's sarcoma (KS) associated with active human herpesvirus 8 (HHVโ€8) infection. He was treated with sequential antiviral therapy, chemotherapy, and corticosteroids. HHVโ€8 levels were monitored throughout the course of the patient's illness, and were found to rise on relapse. No consistent change in HHVโ€8 levels was found with antiviral therapy. We demonstrate that in this patient antiviral therapy was clinically ineffective, and did not alter HHVโ€8 levels, but that corticosteroid and combination chemotherapy led to clinical improvement. Despite the implication of HHVโ€8 as a cause of MCD, few studies have correlated HHVโ€8 levels with clinical response. J. Med. Virol. 71:399โ€“403, 2003. ยฉ 2003 Wileyโ€Liss, Inc.


๐Ÿ“œ SIMILAR VOLUMES


HIV-associated multicentric Castleman's
โœ Justin Stebbing; Liron Pantanowitz; Farshid Dayyani; Ryan J. Sullivan; Mark Bowe ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 427 KB ๐Ÿ‘ 1 views

## Abstract Multicentric Castleman's disease (MCD), a relatively rare lymphoproliferative disorder that presents with heterogenous symptoms including fevers, anemia, and multifocal lymphadenopathy, is today most commonly observed in individuals infected with human immunodeficiency virus typeโ€1 (HIV

A successfully treated case of multicent
โœ Pavlidis, Nicholas A. ;Skopouli, Fotini N. ;Bai, Mary C. ;Bourantas, Constantino ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 297 KB

## Abstract A case of angiofollicular lymph node hyperplasia of plasma cell type in a 60โ€yearโ€old woman is reported. The patient presented with lymphadenopathy, splenomegaly, and fever. She responded dramatically to chlorambucil and corticosteroids and has remained free of disease for the last 30 m