Anti-glomerular basement membrane diseases and thrombotic microangiopathy treated with rituximab

被引:1
|
作者
Honda, Nanase [1 ,2 ,4 ]
Shigehara, Rihiro [1 ]
Furuhashi, Kazunori [1 ,3 ]
Nagai, Yoshiki [1 ,2 ]
Yokogawa, Naoto [1 ,2 ]
机构
[1] Hino Municipal Hosp, Dept Internal Med, Tokyo, Japan
[2] Tokyo Metropolitan Tama Med Ctr, Dept Rheumat Dis, Tokyo, Japan
[3] Keio Univ, Dept Internal Med, Div Rheumatol, Sch Med, Tokyo, Japan
[4] Hino Municipal Hosp, Dept Gen Internal Med, 4-3-1 Tamadaira, Hino, Tokyo 1910062, Japan
关键词
Anti-glomerular basement membrane diseases; secondary thrombotic microangiopathy; rituximab; anti-glomerular basement membrane antibody; ADAMTS-13; THROMBOCYTOPENIC PURPURA; ANTIBODY DISEASE; SECONDARY;
D O I
10.1093/mrcr/rxac091
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 68-year-old male patient presented with a 2-week history of malaise and anuria. Renal replacement therapy with haemodialysis was begun for acute kidney injury. His anti-glomerular basement membrane (anti-GBM) antibody titre was 3060 U/ml. Based on this finding, anti-GBM disease was diagnosed. Plasmapheresis and high-dose glucocorticoid therapy were begun, but his haemolytic anaemia and thrombocytopenia progressed. A disintegrin and metalloprotease with thrombospondin type 1 motif, 13 (ADAMTS-13) activity decreased to 33%, but no inhibitor was detected. Secondary thrombotic microangiopathy was suspected, and rituximab therapy was begun. The addition of rituximab is thought to have further reduced the anti-GBM antibodies, prevented recurrence, stabilised the platelet count, and facilitated the patient's withdrawal from plasmapheresis and glucocorticoid therapy. Rituximab may be a viable therapeutic option for anti-GBM diseases complicated with thrombotic microangiopathy.
引用
收藏
页码:422 / 425
页数:4
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