| Literature DB >> 29737040 |
Toshihiro Araki1, Teruko Arinaga-Hino1, Hironori Koga1,2, Jun Akiba3, Tatsuya Ide1, Yoshinobu Okabe1, Reiichiro Kuwahara1, Keisuke Amano1, Makiko Yasumoto1, Toshihiro Kawaguchi1, Tomoya Sano1, Reiichiro Kondou3, Seiji Kurata4, Keiichi Mitsuyama1, Takuji Torimura1.
Abstract
Immunoglobulin (Ig)G4-related autoimmune hepatitis (AIH) is a recently proposed subtype that responds well to steroid treatment; however, its pathogenesis remains unclear. We report here a 65-year-old Japanese woman with skin itching and lip swelling. She had liver injury with jaundice, which persisted despite stopping anti-allergic agents. Blood chemistry revealed highly elevated serum IgG and IgG4 (535 mg/dL) levels, and positive anti-nuclear antibody. The diagnosis of AIH was based on liver biopsy. Notably, the IgG4+ /IgG+ cell ratio was 85%. On fluorodeoxyglucose (FDG) positron emission tomography/computed tomography, robust signal intensity was found in the liver, and in enlarged lymph nodes and salivary glands with confirmed IgG4+ cell infiltration. Immunofluorescence analysis of the liver biopsy specimen indicated clear expression of glucose transporter-3 (Glut-3) in IgG4+ inflammatory cells infiltrating into the portal area. This is the first report of simultaneous strong accumulation of FDG and Glut-3 expression in IgG4-related AIH, which might aid in elucidating the pathogenesis of this disease.Entities:
Keywords: AIH; FDG-PET/CT; IgG4-related AIH; IgG4-related disease; double immunofluorescence staining; glucose transporter (Glut)
Year: 2018 PMID: 29737040 DOI: 10.1111/hepr.13188
Source DB: PubMed Journal: Hepatol Res ISSN: 1386-6346 Impact factor: 4.288