Vasquez Moises A, Andrade-Bucknor Sharon
Department of Internal Medicine University of Miami Miller School of Medicine/Jackson Memorial Hospital Miami Florida USA.
Department of Medicine, Department of Cardiovascular Diseases University of Miami Miller School of Medicine Miami Florida USA.
Clin Case Rep. 2024 Jul 16;12(7):e9035. doi: 10.1002/ccr3.9035. eCollection 2024 Jul.
Isolated cardiac sarcoidosis may rarely present with TIA or stroke as an initial clinical manifestation. This case highlights the necessity of a broad differential and a high degree of suspicion for cardiac sarcoidosis in a patient with new neurologic symptoms and evidence of cardiac disease.
Cardiac sarcoidosis is a rare disease with a variety of clinical manifestations including heart failure and sudden death. Stroke as the earliest sign of disease has been described in rare cases. We present a case of a 54-year-old female with recurrent transient ischemic attacks (TIAs) of unknown etiology, initially in the absence of left ventricular dysfunction. Cardiomyopathy was later identified on echocardiography after a second TIA. Cardiac MRI was remarkable for focal left ventricular wall thinning with akinesis and dyskinesis of multiple wall segments, a right ventricular aneurysm, and diffuse myocardial late gadolinium enhancement. PET/CT showed multifocal areas of myocardial FDG uptake. At follow-up, echocardiography showed a left ventricular apical thrombus, in a previously identified thinned, akinetic region, suggesting cardioembolic origin for previous TIAs. She was started on anticoagulation therapy, prednisone, methotrexate, and adalimumab, with resolution of the thrombus and improvement in cardiac function. In conclusion, this case highlights the need to consider CS as a potential cause of cerebrovascular ischemic events in patients with few stroke risk factors but findings indicative of cardiac disease. It is essential to further explore the mechanisms behind these events and develop treatments that target their causes in this patient population.
孤立性心脏结节病很少会以短暂性脑缺血发作(TIA)或中风作为初始临床表现。该病例强调了对于出现新的神经系统症状且有心脏病证据的患者,进行广泛鉴别诊断并高度怀疑心脏结节病的必要性。
心脏结节病是一种罕见疾病,有多种临床表现,包括心力衰竭和猝死。在罕见病例中曾有将中风描述为该病最早体征的情况。我们报告一例54岁女性,病因不明的复发性短暂性脑缺血发作(TIA),最初并无左心室功能障碍。在第二次TIA发作后,经超声心动图检查发现了心肌病。心脏磁共振成像(MRI)显示左心室壁局灶性变薄,多个壁节段运动减弱和运动障碍,右心室动脉瘤,以及弥漫性心肌延迟钆增强。正电子发射断层扫描/计算机断层扫描(PET/CT)显示心肌氟代脱氧葡萄糖(FDG)摄取的多灶性区域。随访时,超声心动图显示在先前确定的变薄、运动减弱区域出现左心室心尖血栓,提示先前TIA发作的心源性栓塞起源。她开始接受抗凝治疗、泼尼松、甲氨蝶呤和阿达木单抗治疗,血栓溶解,心脏功能改善。总之,该病例强调了对于中风风险因素较少但有心脏病迹象的患者,需要考虑心脏结节病作为脑血管缺血事件的潜在原因。进一步探索这些事件背后的机制并开发针对该患者群体病因的治疗方法至关重要。