Clinicopathologic Features of Adult-onset Still’s Disease Complicated by Severe Liver Injury

Miho Kurokawa, Tomonobu Hioki, Tomomi Aoyagi, Motoi Takahashi, Koji Imoto, Takeshi Goya, Masatake Tanaka, Motoyuki Kohjima, Yoshihiro Ogawa

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Adult-onset Still’s disease (AOSD) is a systemic inflammatory disorder. Severe liver injury has rarely been reported, although liver enzyme elevation is a common complication of AOSD. We herein report four cases of relapsed AOSD with severe liver disorder by tapering or terminating corticosteroids. Liver specimens revealed robust infiltration of inflammatory cells throughout the lobule, especially cluster of differentiation (CD) 8-positive cells. Relapsed AOSD was refractory to corticosteroid reintroduction and required immunosuppressants. Severe liver injury with AOSD is pathologically characterized by extensive lobular infiltration of CD8-positive cells, and we should consider additive immunosuppressive agents on corticosteroids for treatment.

Original languageEnglish
Pages (from-to)503-511
Number of pages9
JournalInternal Medicine
Volume63
Issue number4
DOIs
Publication statusPublished - 2024

All Science Journal Classification (ASJC) codes

  • Internal Medicine

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