| Literature DB >> 17971092 |
Kiyoshi Migita1, Seigo Abiru, Mototsugu Tanaka, Masahiro Ito, Taichiro Miyashita, Yumi Maeda, Tomohiro Koga, Minoru Nakamura, Atsumasa Komori, Hiroshi Yatsuhashi, Hiroaki Ida, Katsumi Eguchi, Kenji Hirayama, Michio Yasunami, Hiromi Ishibashi.
Abstract
Familial Mediterranean fever (FMF) is a hereditary syndrome characterized by recurrent episodes of fever and serositis. In this report, we describe a Japanese patient with FMF and Sjögren's syndrome, in whom acute elevations of transaminase occurred. The histological findings from the liver biopsy specimens demonstrated a nonspecific hepatitis, with liver cell necrosis and interlobular inflammatory cell invasion, without the presence of interface hepatitis or bile duct injury. This case underscores the possibility that MEFV mutations contribute to hepatic inflammation, as seen in this case, by way of an alteration of the pyrin function.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17971092 DOI: 10.1111/j.1478-3231.2007.01598.x
Source DB: PubMed Journal: Liver Int ISSN: 1478-3223 Impact factor: 5.828