Antiphospholipid Syndrome Nephropathy with Acute Thrombotic Microangiopathy after Renal Transplantation

被引:2
作者
Suenaga, Atsuhiko [1 ]
Sawa, Naoki
Miki, Katsuyuki
Yokoyama, Takayoshi
Ishii, Yasuo
Mizuno, Hiroki
Ikuma, Daisuke
Oba, Yuki
Sekine, Akinari
Yamanouchi, Masayuki
Hasegawa, Eiko
Suwabe, Tatsuya
Kono, Kei
Kinowaki, Keiichi
Ohashi, Kenichi
Honda, Kazuho
Miyazono, Motoaki
Nakamura, Yuki
Ubara, Yoshifumi
机构
[1] Toranomon Hosp Kajigaya, Dept Nephrol & Rheumatol, Kawasaki, Kanagawa, Japan
关键词
antiphospholipid syndrome; antiphospholipid syndrome nephropathy; renal transplantation; thrombotic microangiopathy; lupus nephropathy; LESIONS;
D O I
10.2169/internalmedicine.0813-22
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We experienced a 36-year-old man with lupus nephritis and antiphospholipid syndrome (APS) who re-ceived a donor kidney from his father. Twenty-two months after transplantation, at a time of poor adherence to immunosuppressants and warfarin, the patient developed sudden graft loss due to hemolytic uremic syn-drome with rapid deterioration of renal function, thrombocytopenia, and hemolytic anemia. A kidney biopsy showed thrombotic microangiopathy (TMA) related to platelet thrombus formation; however, there was no re-currence of lupus and no findings suggestive of post-transplant rejection, so acute TMA associated with APS was thought to be the cause of the graft loss. This case highlights the importance of instructing patients with lupus nephritis to adhere to treatment with warfarin, a therapeutic drug for APS.
引用
收藏
页码:2707 / 2713
页数:7
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