利妥昔单抗治疗抗肾小球基底膜疾病和血栓性微血管病。

Nanase Honda, Rihiro Shigehara, Kazunori Furuhashi, Yoshiki Nagai, Naoto Yokogawa
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引用次数: 2

摘要

68岁男性患者,有2周的不适和无尿史。急性肾损伤开始血液透析肾替代治疗。抗肾小球基底膜(anti-GBM)抗体滴度3060 U/ml。基于这一发现,诊断为抗gbm疾病。开始血浆置换和大剂量糖皮质激素治疗,但他的溶血性贫血和血小板减少症进展。具有血小板反应蛋白1型基元的崩解素和金属蛋白酶13 (ADAMTS-13)活性下降至33%,但未检测到抑制剂。怀疑继发性血栓性微血管病变,开始美罗华治疗。利妥昔单抗的加入被认为进一步降低了抗gbm抗体,防止复发,稳定血小板计数,并促进患者退出血浆置换和糖皮质激素治疗。利妥昔单抗可能是抗gbm疾病合并血栓性微血管病变的可行治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-glomerular basement membrane diseases and thrombotic microangiopathy treated with rituximab.

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.

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