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A Case of Hepatic Inflammatory Pseudotumor Occurred in a Patient with Lupus Nephritisopen access

Authors
Kim, Min JungKim, HyoungyoungSong, Yeo-JinCho, Soo-KyungSung, Yoon-Kyoung
Issue Date
Apr-2019
Publisher
KOREAN COLL RHEUMATOLOGY
Keywords
Systemic lupus erythematosus; Liver neoplasm; Granuloma; Plasma cell
Citation
JOURNAL OF RHEUMATIC DISEASES, v.26, no.2, pp.137 - 141
Indexed
KCI
Journal Title
JOURNAL OF RHEUMATIC DISEASES
Volume
26
Number
2
Start Page
137
End Page
141
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/14242
DOI
10.4078/jrd.2019.26.2.137
ISSN
2093-940X
Abstract
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease affecting various organs. Among its manifestations, inflammatory pseudotumor (IPT) is an extremely rare disease about which no case has been reported of it occurring in the liver. We present a case of a SLE patient with hepatic IPT (hIPT) successfully treated with immunosuppressants. A 16-year-old male with elevated liver enzymes visited our clinic and was diagnosed as SLE. Although no lesion was observed in the initial abdomen ultrasonography, the abdominal CT on hospital day 7 revealed a new hepatic mass resembling an abscess. Despite 5 weeks of antibiotics treatment, the hepatic mass remained, and was re-diagnosed as hIPT secondary to SLE with an abdominal MRI. After high dose prednisolone and mycophenolate mofetil treatment, lupus activity subsided and hIPT disappeared in the follow-up CT. This case suggests that hIPT should be considered as a differential diagnosis among hepatic mass in SLE patients.
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