Gonçalves Francisco, Duarte Daniela, Reis Filipa, Vaz Alexandra, Gomes Ana
Internal Medicine, Centro Hospitalar Tondela-Viseu, Viseu, PRT.
Stroke Unit, Centro Hospitalar Tondela-Viseu, Viseu, PRT.
Cureus. 2024 Nov 14;16(11):e73702. doi: 10.7759/cureus.73702. eCollection 2024 Nov.
Cold agglutinin disease (CAD) is a rare autoimmune hemolytic anemia caused by cold-reactive IgM antibodies leading to complement-mediated hemolysis. While CAD-associated venous thromboembolism is recognized, its role in arterial thromboembolic events, particularly ischemic stroke, is poorly defined. We report an 84-year-old woman who developed acute onset upper left extremity weakness following exposure to sub-zero temperatures. She had a history of similar transient episodes during cold seasons and recurrent anemia. Physical examination revealed decreased muscle strength in the upper left extremity (Grade 4+ out of 5) and scleral icterus. Laboratory findings showed normocytic anemia, elevated reticulocytes, high lactate dehydrogenase, indirect hyperbilirubinemia, and undetectable haptoglobin levels. Peripheral smear showed erythrocyte agglutination. Direct antiglobulin test was positive for C3d and IgM, confirming CAD. Vascular imaging showed significant atherosclerotic disease with near-occlusive (>80%) stenosis of the right internal carotid artery. The patient's transient ischemic attacks were attributed to compromised cerebral perfusion due to severe carotid artery stenosis, exacerbated by anemia from cold-induced hemolysis in CAD. Cold exposure precipitated hemolysis, leading to acute anemia and increased blood viscosity, further reducing cerebral blood flow and oxygen delivery. Spontaneous resolution of symptoms upon rewarming supported the role of CAD in her neurological deficits. This case underscores the potential for CAD to induce neurological deficits in patients with significant carotid artery stenosis. Clinicians should consider CAD as a contributory factor in patients presenting with transient neurological deficits precipitated by cold exposure, especially when significant arterial stenosis is present.
冷凝集素病(CAD)是一种罕见的自身免疫性溶血性贫血,由冷反应性IgM抗体引起,导致补体介导的溶血。虽然CAD相关的静脉血栓栓塞已得到认可,但其在动脉血栓栓塞事件,特别是缺血性卒中中的作用尚不清楚。我们报告一名84岁女性,在暴露于零下温度后出现急性发作的左上肢体无力。她有在寒冷季节类似短暂发作和反复贫血的病史。体格检查发现左上肢体肌力下降(5级中的4+级)和巩膜黄疸。实验室检查结果显示正细胞性贫血、网织红细胞升高、乳酸脱氢酶升高、间接胆红素血症以及触珠蛋白水平检测不到。外周血涂片显示红细胞凝集。直接抗球蛋白试验C3d和IgM呈阳性,确诊为CAD。血管成像显示严重的动脉粥样硬化疾病,右颈内动脉近闭塞(>80%)狭窄。患者的短暂性脑缺血发作归因于严重颈动脉狭窄导致的脑灌注受损,CAD中寒冷诱导的溶血导致的贫血使其加重。寒冷暴露引发溶血,导致急性贫血和血液粘度增加,进一步减少脑血流量和氧气输送。复温后症状自发缓解支持了CAD在其神经功能缺损中的作用。该病例强调了CAD在有严重颈动脉狭窄的患者中诱发神经功能缺损的可能性。临床医生应将CAD视为在寒冷暴露引发短暂性神经功能缺损的患者中的一个促成因素,尤其是当存在严重动脉狭窄时。