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Case Reports

A case of eosinophilic granulomatosis with polyangiitis as a mimicker of IgG4-related disease

ORCID Icon, , , , , , & ORCID Icon show all
Pages 278-282 | Received 09 Jan 2020, Accepted 13 Apr 2020, Published online: 07 May 2020
 

Abstract

A 62-year-old woman was admitted to our hospital because of fever, renal dysfunction, eosinophilia, and the presence of MPO-ANCA. Based on the renal pathological examination which showed granuloma lesion with eosinophils and crescentic glomerulonephritis, eosinophilic granulomatosis with polyangiitis (EGPA) was diagnosed. On the other hand, laboratory examination showed elevated serum IgG4 levels and renal pathological examination showed marked lymphoplasmacytic infiltration and fibrosis surrounding nest “Bird’s eye pattern,” which were characteristic of IgG4-related kidney disease (IgG4-RKD). Because there are cases when EGPA has clinical features of IgG4-RKD, we should be careful about diagnoses of IgG4-RKD in patients with EGPA.

Patient consent

Written informed consent was obtained from the patient for this case report.

Ethical approval

Ethical Approval is not applicable.

Conflict of interest

S. Kubo has received speaking fees from Bristol-Myers, Pfizer, Takeda, and Eli Lilly and also research grants from Glaxo-Smithkline. Y. Tanaka has received speaking fees and/or honoraria from Daiichi-Sankyo, Astellas, Chugai, Eli Lilly, Pfizer, Abbvie, YL Biologics, Bristol-Myers, Takeda, Mitsubishi-Tanabe, Novartis, Eisai, Janssen, Teijin and has received research grants from Asahi-kasei, Mitsubishi-Tanabe, Chugai, Takeda, Sanofi, Bristol-Myers, UCB, Daiichi-Sankyo, Eisai, Ono. All other authors have declared no conflicts of interest.

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