Service of Neurology, University Hospital Marqués de Valdecilla, Santander, Spain.
J Stroke Cerebrovasc Dis. 2012 Aug;21(6):515-7. doi: 10.1016/j.jstrokecerebrovasdis.2010.12.003. Epub 2011 Feb 3.
We report a patient who experienced multiple transient ischemic attacks (TIAs) over a 3-month period as the presenting clinical manifestation of sarcoidosis. This previously healthy 27-year-old man was admitted due to several daily episodes of usually left hemiparesis and dysarthria lasting between 15 seconds and 3 minutes. He did not respond to aggressive antithrombotic treatment. Extensive investigations were negative except for a computed tomography body scan showing several small right hilar lymphoadenopathies, which were confirmed by abnormal 67-gallium scintigraphy and 18F-fluorodeoxyglucose positron emission tomography uptakes. The TIA episodes disappeared after the initiation of prednisone therapy. The lymphadenopathy specimens were biopsied via mediastinoscopy, and histological study revealed noncaseating epithelioid granulomatous inflammation consistent with sarcoidosis. Sarcoidosis should be considered in the differential diagnosis of stroke of unknown origin in any young patient, even in the absence of other clinical or laboratory features of sarcoidosis.
我们报告了一例患者,其在 3 个月期间经历了多次短暂性脑缺血发作(TIA),这是结节病的首发临床表现。这位之前健康的 27 岁男性因每天数次短暂性左侧偏瘫和构音障碍而入院,每次发作持续 15 秒至 3 分钟。他对强化抗血栓治疗没有反应。除了计算机断层扫描全身扫描显示几个较小的右侧肺门淋巴结肿大外,广泛的检查均为阴性,这些淋巴结肿大通过异常的 67 镓闪烁扫描和 18F-氟脱氧葡萄糖正电子发射断层扫描摄取得到证实。泼尼松治疗开始后,TIA 发作消失。通过纵隔镜对淋巴结进行活检,组织学研究显示非干酪样上皮样肉芽肿性炎症,符合结节病。在任何年轻患者中,即使没有结节病的其他临床或实验室特征,也应考虑将其作为不明原因中风的鉴别诊断之一。