Kimura Shunsuke, Osaki Masato, Sakai Shota, Ohya Yuichiro, Ago Tetsuro, Kitazono Takanari, Arakawa Shuji
Department of Cerebrovascular Medicine, Steel Memorial Yawata Hospital.
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University.
Nihon Ronen Igakkai Zasshi. 2019;56(3):331-335. doi: 10.3143/geriatrics.56.331.
A 79-year-old woman came to us because of sudden onset of dysarthria. She had taken apixaban due to her non-valvular atrial fibrillation. A neurological examination revealed mild facial palsy of her right side, and magnetic resonance imaging showed acute brain infarction at the left frontal lobe. There were no stenotic lesions on intracranial or extracranial magnetic resonance angiography, and she was diagnosed with cardioembolic stroke. Intravenous infusion of heparin and edaravone was initiated, and her neurological symptoms improved. However, she gradually developed jaundice and anemia. Gastro-intestinal bleeding was not observed, and her blood test met the diagnostic criteria for hemolytic anemia. Because both the direct Coombs test and cold agglutinin were positive, she was diagnosed with mixed-type autoimmune hemolytic anemia. Although her serum hemoglobin level decreased to 7.0 g/dl on the 12th hospital day, her anemia gradually improved after steroidal therapy with transfusion. It was revealed that she had shown mild anemia (hemoglobin: 9.2-10.9 g/dl) and hyperbilirubinemia (total bilirubin: 1.8-2.6 mg/dl) for 6 months. Therefore, her latent autoimmune hemolytic anemia became activated with the occurrence of cardioembolic stroke. Autoimmune hemolytic anemia might have promoted cardiac thrombus formation despite the administration of an anticoagulant in this case. It should be noted that autoimmune hemolytic anemia can develop as thrombotic disease. In the present case, autoimmune hemolytic anemia was diagnosed based on the development of cardioembolic stroke.
一名79岁女性因突然出现构音障碍前来就诊。她因非瓣膜性心房颤动服用阿哌沙班。神经系统检查发现右侧轻度面瘫,磁共振成像显示左侧额叶急性脑梗死。颅内和颅外磁共振血管造影未发现狭窄病变,她被诊断为心源性栓塞性中风。开始静脉输注肝素和依达拉奉,其神经症状有所改善。然而,她逐渐出现黄疸和贫血。未观察到胃肠道出血,血液检查符合溶血性贫血的诊断标准。由于直接抗人球蛋白试验和冷凝集素均呈阳性,她被诊断为混合型自身免疫性溶血性贫血。虽然她的血清血红蛋白水平在住院第12天时降至7.0 g/dl,但在输血的类固醇治疗后贫血逐渐改善。结果发现她在6个月内一直存在轻度贫血(血红蛋白:9.2 - 10.9 g/dl)和高胆红素血症(总胆红素:1.8 - 2.6 mg/dl)。因此,她潜在的自身免疫性溶血性贫血因心源性栓塞性中风的发生而被激活。在这种情况下,尽管使用了抗凝剂,但自身免疫性溶血性贫血可能促进了心脏血栓形成。应当注意,自身免疫性溶血性贫血可作为血栓性疾病发生。在本病例中,基于心源性栓塞性中风的发生诊断出自身免疫性溶血性贫血。