双氯芬酸治疗相关的严重可逆性自身免疫性溶血性贫血和血小板减少症。

M R Kramer, C Levene, C Hershko
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引用次数: 35

摘要

严重的免疫性溶血性贫血和血小板减少症在开始双氯芬酸(伏他罗)治疗10天内发生在71岁女性。这些并发症在停药和皮质类固醇治疗后3周内消失。在患者红细胞直接抗球蛋白试验中发现IgG型和C3型温热自身抗体。患者的血清和红细胞洗脱液中含有一种温热自身抗体,该抗体在不添加双氯芬酸的情况下与所有商业面板细胞反应,并与Rh null和d - RBC呈阴性反应。这种相互作用的模式类似于与α -甲基多巴相关的溶血,表明存在针对所有Rh抗原共同结构成分的自身抗体。免疫性血小板减少症和免疫性溶血性贫血的共存提示一种由修改的t细胞调节引起的自身免疫性疾病。虽然免疫性溶血性贫血是双氯芬酸治疗的罕见并发症,但我们的观察结果表明,偶尔患者出现溶血性贫血的严重程度,并强调需要提高对这种发展的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe reversible autoimmune haemolytic anaemia and thrombocytopenia associated with diclofenac therapy.

Severe immune haemolytic anaemia and thrombocytopenia developed in a 71-year-old female within 10 d of starting diclofenac (Voltarol) therapy. These complications resolved within 3 weeks of discontinuation of the drug and corticosteroid therapy. A warm autoantibody of the IgG type together with C3 was found in the direct antiglobulin test of the patient's RBC. The patient's serum and RBC eluate contained a warm autoantibody which reacted with all commercial panel cells without the addition of diclofenac, and gave a negative reaction with Rh null and -D- RBC. This pattern of interactions is similar to haemolysis associated with alpha-methyldopa, indicating the presence of autoantibodies directed against structural components common to all Rh antigens. The coexistence of immune thrombocytopenia and immune haemolytic anaemia is suggestive of an autoimmune disease caused by modified T-cell regulation. Although immune haemolytic anaemia is a rare complication of diclofenac therapy, our observations illustrate the severity of haemolytic anaemia in the occasional patient and stress the need for increased awareness of such a development.

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