Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report

被引:2
作者
Sofue, Tadashi [1 ]
Hayashida, Yushi [2 ]
Hara, Taiga [1 ]
Kawakami, Kazuyo [1 ]
Ueda, Nobufumi [2 ]
Kushida, Yoshio [3 ]
Inui, Masashi [4 ]
Dobashi, Hiroaki [5 ]
Kakehi, Yoshiyuki [2 ]
Kohno, Masakazu [1 ]
机构
[1] Kagawa Univ, Fac Med, Div Nephrol & Dialysis, Dept CardioRenal & Cerebrovasc Med, Miki, Kagawa 7610793, Japan
[2] Kagawa Univ, Dept Urol, Miki, Kagawa 7610793, Japan
[3] Kagawa Univ, Dept Pathol, Miki, Kagawa 7610793, Japan
[4] Tokyo Womens Med Univ, Yachiyo Med Ctr, Dept Urol, Chiba 2768524, Japan
[5] Kagawa Univ, Dept Internal Med, Div Endocrinol & Metab Hematol Rheumatol & Resp M, Miki, Kagawa 7610793, Japan
关键词
Antiphospholipid syndrome; Living-donor kidney transplantation; Plasmapheresis; Anti-beta 2-glycoprotein I IgG; PLASMA-EXCHANGE; ANTIBODY SYNDROME; RENAL-ALLOGRAFT; I ANTIBODIES; RITUXIMAB; MANAGEMENT; EFFICACY; PREDNISOLONE; PATHOGENESIS; THROMBOSIS;
D O I
10.1186/1471-2369-15-167
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Early graft thrombosis and bleeding complications remain important causes of early graft loss following kidney transplantation in patients with antiphospholipid syndrome. Anti-beta 2-glycoprotein I IgG is a disease-specific antibody in patients with antiphospholipid syndrome. Although plasmapheresis is partially effective for antibody removal, the optimal treatment allowing successful transplantation in patients with antiphospholipid syndrome has not been established. This is the first report of a patient with antiphospholipid syndrome who successfully underwent living-donor kidney transplantation following prophylactic plasmapheresis for removal of anti-beta 2-glycoprotein I IgG. Case presentation: A 37-year-old Japanese female was scheduled to undergo a living-donor kidney transplant from her mother. At age 25 years, she experienced renal vein thrombosis, was diagnosed with antiphospholipid syndrome secondary to systemic lupus erythematosus, and was subsequently treated with prednisolone and warfarin. At age 37 years, she was diagnosed with end stage kidney disease, requiring maintenance hemodialysis because of recurrent renal vein thrombosis despite taking anticoagulation therapy. The pretreatment protocol consisted of prophylactic plasmapheresis plus full anticoagulation therapy to counteract the risks of early graft thrombosis. Anticardiolipin and anti-beta 2-glycoprotein I IgGs were successfully removed by both double filtration plasmapheresis and plasma exchange. The allograft kidney began to function soon after transplantation. No obvious thrombotic complications were observed after transplantation, although anti-beta 2-glycoprotein I IgG increased to the level observed before plasmapheresis. One year after transplantation, the patient's kidney function remains stable while receiving anticoagulation therapy as well as a maintenance immunosuppressive regimen. Conclusion: Prophylactic plasmapheresis plus full anticoagulation therapy may be an effective strategy in patients with antiphospholipid syndrome undergoing living-donor kidney transplantation.
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页数:6
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