Primary IgA Vasculitis with Nephritis in a Patient with Rheumatoid Arthritis Diagnosed by Anti-galactose-deficient IgA1 Immunostaining

Renal disease is a common complication of rheumatoid arthritis (RA) and can occur secondary to RA or be induced by therapeutic agents. Recently, glomerular deposition of galactose-deficient IgA1 (Gd-IgA1) was identified as a feature of primary IgA vasculitis with nephritis (IgA-VN). We herein report...

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Veröffentlicht in:Internal Medicine 2019/09/01, Vol.58(17), pp.2551-2554
Hauptverfasser: Karasawa, Kazunori, Iwabuchi, Yuko, Kyoda, Mizuki, Akihisa, Taro, Yamaguchi, Erika, Suzuki, Shunji, Ogura, Shota, Takabe, Tomo, Miyabe, Yoei, Kamiyama, Takahiro, Nakano, Marie, Manabe, Shun, Kamiyama, Michiaki, Akiyama, Kenichi, Sato, Masayo, Uchida, Keiko, Nitta, Kosaku, Moriyama, Takahito
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Sprache:eng
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Zusammenfassung:Renal disease is a common complication of rheumatoid arthritis (RA) and can occur secondary to RA or be induced by therapeutic agents. Recently, glomerular deposition of galactose-deficient IgA1 (Gd-IgA1) was identified as a feature of primary IgA vasculitis with nephritis (IgA-VN). We herein report a case of IgA-VN in an RA patient whose disease activity was controlled by treatment with etanercept. To distinguish between primary IgA-VN and secondary IgA-VN caused by RA or etanercept, we performed immunostaining of renal biopsy sections with the Gd-IgA1-specific antibody KM55. Positive KM55 staining confirmed the diagnosis of primary IgA-VN in a patient with RA.
ISSN:0918-2918
1349-7235
DOI:10.2169/internalmedicine.2640-19