| Literature DB >> 28509128 |
Fumiaki Obata1, Taichi Murakami2, Junko Miyagi3, Sayo Ueda1, Taizo Inagaki1, Masanori Minato1, Hiroyuki Ono1, Kenji Nishimura1, Eriko Shibata1, Masanori Tamaki1, Sakiya Yoshimoto1, Fumi Kishi1, Seiji Kishi1, Motokazu Matsuura1, Kojiro Nagai1, Hideharu Abe1, Toshio Doi1.
Abstract
Mixed cryoglobulinemic syndrome, which is a systemic vasculitis characterized by the immune complex deposition in small- and medium-sized arteries and most often due to chronic hepatitis C virus (HCV) infection, sometimes clinically manifests as refractory glomerulonephritis or nephritic syndrome. Patients with mixed cryoglobulinemic nephropathy who have a rapidly progressive glomerulonephritis should receive immunosuppressive therapy. After disease stabilization, patients should receive concurrent therapy for the underlying HCV infection. The standard therapy of a chronic HCV infection is IFN monotherapy or IFN combined with ribavirin; however, after the introduction of direct-acting antivirals (DAAs), the standard therapy for patients with HCV genotype 1 has dramatically changed. We report a case of HCV-associated cryoglobulinemic membranoproliferative glomerulonephritis (MPGN) successfully treated by daclatasvir and asunaprevir, which are IFN-free DAAs for HCV, in combination with angiotensin II receptor blocker without immunosuppressive therapy. The patient developed severe nephrotic syndrome with progressive kidney dysfunction. Blood examination revealed a high copy number of HCV-RNA (6.4 log IU/mL, type 1), cryoglobulinemia, paraproteinemia of IgM-κ, and hypocomplementemia. Histological analysis showed MPGN type 1. These findings were compatible with those observed in HCV-associated cryoglobulinemic MPGN. This case offers original evidence for the application of newer generation of IFN-free DAAs in the treatment of HCV-associated cryoglobulinemic nephropathy.Entities:
Keywords: Cryoglobulinemic membranoproliferative glomerulonephritis; Hepatitis C virus; Interferon-free direct-acting antiviral agents
Year: 2016 PMID: 28509128 PMCID: PMC5438808 DOI: 10.1007/s13730-016-0244-z
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449