Eculizumab reversed severe distal ischemic syndrome and glomerulonephritis with isolated C3 deposits associated with anti-factor H autoantibodies: a case report

被引:0
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作者
Samuel Deshayes
Nicolas Martin Silva
Valérie Chatelet
Sylvain Chantepie
Moglie Le Quintrec
François Comoz
Frank Bridoux
Marie-Agnès Dragon-Durey
Achille Aouba
机构
[1] CHU Côte de Nacre—Université Basse Normandie,Department of Internal Medicine and Clinical Immunology
[2] CHU de Caen,Department of Nephrology
[3] CHU de Caen,Department of Clinical Hematology
[4] CHU de Lapeyronie,Service de Transplantation et Néphrologie
[5] CHU de Caen,Department of Anatomopathology
[6] CHU de Poitiers,Department of Nephrology and Transplantation and Centre national de référence maladies rares: amylose AL et autres maladies à depôts d’immunoglobulines monoclonales
[7] Hôpital Européen Georges Pompidou,Department of Biological Immunology, Assistance Publique
来源
Clinical Rheumatology | 2018年 / 37卷
关键词
C3 glomerulopathies; Digital ischemia; Eculizumab; Factor H antibody;
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学科分类号
摘要
B-cell clones can produce a monoclonal immunoglobulin, which may be responsible for visceral involvements. Kidney involvement is frequent, affecting 20 to 50% of patients with multiple myeloma. One mechanism underlying this involvement is a dysregulation of the complement alternative pathway, leading to C3 glomerulopathies. We report a patient who had a multiple myeloma, C3 glomerulopathy related to factor H autoantibody, and digital ischemia, who was treated successfully with eculizumab, an anti-complement therapy, without any relapse in 2 years of follow-up.
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页码:1119 / 1122
页数:3
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