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Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report
BACKGROUND: Early graft thrombosis and bleeding complications remain important causes of early graft loss following kidney transplantation in patients with antiphospholipid syndrome. Anti-β2-glycoprotein I IgG is a disease-specific antibody in patients with antiphospholipid syndrome. Although plasma...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216348/ https://www.ncbi.nlm.nih.gov/pubmed/25319344 http://dx.doi.org/10.1186/1471-2369-15-167 |
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author | Sofue, Tadashi Hayashida, Yushi Hara, Taiga Kawakami, Kazuyo Ueda, Nobufumi Kushida, Yoshio Inui, Masashi Dobashi, Hiroaki Kakehi, Yoshiyuki Kohno, Masakazu |
author_facet | Sofue, Tadashi Hayashida, Yushi Hara, Taiga Kawakami, Kazuyo Ueda, Nobufumi Kushida, Yoshio Inui, Masashi Dobashi, Hiroaki Kakehi, Yoshiyuki Kohno, Masakazu |
author_sort | Sofue, Tadashi |
collection | PubMed |
description | BACKGROUND: Early graft thrombosis and bleeding complications remain important causes of early graft loss following kidney transplantation in patients with antiphospholipid syndrome. Anti-β2-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-β2-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-β2-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-β2-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. |
format | Online Article Text |
id | pubmed-4216348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42163482014-11-02 Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report Sofue, Tadashi Hayashida, Yushi Hara, Taiga Kawakami, Kazuyo Ueda, Nobufumi Kushida, Yoshio Inui, Masashi Dobashi, Hiroaki Kakehi, Yoshiyuki Kohno, Masakazu BMC Nephrol Case Report BACKGROUND: Early graft thrombosis and bleeding complications remain important causes of early graft loss following kidney transplantation in patients with antiphospholipid syndrome. Anti-β2-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-β2-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-β2-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-β2-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. BioMed Central 2014-10-15 /pmc/articles/PMC4216348/ /pubmed/25319344 http://dx.doi.org/10.1186/1471-2369-15-167 Text en © Sofue et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Sofue, Tadashi Hayashida, Yushi Hara, Taiga Kawakami, Kazuyo Ueda, Nobufumi Kushida, Yoshio Inui, Masashi Dobashi, Hiroaki Kakehi, Yoshiyuki Kohno, Masakazu Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report |
title | Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report |
title_full | Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report |
title_fullStr | Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report |
title_full_unstemmed | Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report |
title_short | Plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report |
title_sort | plasmapheresis in a patient with antiphospholipid syndrome before living-donor kidney transplantation: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216348/ https://www.ncbi.nlm.nih.gov/pubmed/25319344 http://dx.doi.org/10.1186/1471-2369-15-167 |
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