Not Another ACS Rule Out.

S Preston, R Nelson, M Watts, D Smith, T Dewenter, D Spruill
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Abstract

Case: A 50 year old African-American woman with diabetes, hypertension, and hyperlipidemia presented with progressively worsening retro-sternal chest pain, exacerbated by activity and relieved by rest. She also endorsed a thirty-pound unintentional weight loss, and dysphagia. She was dysarthric with left-sided Bell's Palsy and a palpable left axillary lymph node. She had been evaluated at several hospitals in the previous months for similar typical chest pain. Her troponin values were normal, and an EKG showed T-wave inversions in leads I and aVL. On echocardiography, her ejection fraction was 45 percent with anterolateral hypokinesis. She was treated for NSTEMI, and an angiogram showed 95 percent stenosis of the right coronary artery. A modified barium swallow study revealed weakened swallowing with aspiration of thin liquids. An MRI Brain demonstrated scattered T2/ FLAIR hyper-intense foci in the subcortical white matter and focal meningeal thickening. ANA, dsDNA, ANCA, and Lyme antibodies were all negative, and a chest CT showed hilar lymphadenopathy. Cardiac MRI demonstrated scattered foci of delayed enhancement in the mid-myocardium and sub-epicardium without infarction. An endobronchial biopsy of hilar lymph nodes showed two small epithelioid granulomas, consistent with Sarcoidosis. She was started on high-dose corticosteroids with rapid improvement. A repeat modified barium swallow study was normal and a repeat echocardiogram demonstrated recovered ejection fraction of 55 percent with improved wall motion in the septum and apex. Additionally, her left-sided Bell's Palsy and dysarthria improved after several days of therapy.

Discussion: To our knowledge, this report is the third case of multi-organ Sarcoidosis presenting as ACS. This case depicts the simultaneous presentation of neurologic, pharyngeal, pulmonary, and cardiac Sarcoidosis. Myocardial involvement in Sarcoidosis is rare and usually presents as conduction abnormalities with arrhythmia rather than ACS. Though her symptoms were consistent with Sarcoidosis, she had multiple risk factors for coronary atherosclerosis including diabetes, hypertension, and hyperlipidemia. This case highlights the importance of including Sarcoidosis in the differential diagnosis for patients with recurrent typical chest pain of uncertain etiology.

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不是另一个ACS排除。
病例:一名患有糖尿病、高血压和高脂血症的50岁非裔美国女性,表现为逐渐恶化的胸骨后胸痛,活动加重,休息缓解。她还无意中减轻了30磅体重,并出现了吞咽困难。她患有左侧贝尔氏麻痹和可触及的左腋窝淋巴结。在过去的几个月里,她因类似的典型胸痛在几家医院接受了评估。她的肌钙蛋白值正常,心电图显示导联I和aVL的t波反转。超声心动图显示,她的射血分数为45%,伴有前外侧运动不足。她接受了非stemi治疗,血管造影显示95%的右冠状动脉狭窄。一项改良的钡剂吞咽研究显示,吸入稀液体后吞咽减弱。脑MRI显示皮层下白质分散的T2/ FLAIR高强度灶和局灶性脑膜增厚。ANA、dsDNA、ANCA、莱姆病抗体均为阴性,胸部CT显示肺门淋巴结病变。心脏MRI示心肌中部和心外膜下散在灶延迟增强,无梗死。肺门淋巴结支气管活检显示两个小的上皮样肉芽肿,符合结节病。她开始服用大剂量皮质类固醇,病情迅速好转。重复改良钡吞片检查正常,重复超声心动图显示射血分数恢复55%,室间隔和心尖壁运动改善。此外,经过几天的治疗,她的左侧贝尔氏麻痹和构音障碍有所改善。讨论:据我们所知,本报告是第三例以ACS表现的多器官结节病。此病例同时表现为神经、咽、肺和心脏结节病。结节病的心肌受累是罕见的,通常表现为传导异常并伴有心律失常,而不是ACS。虽然她的症状符合结节病,但她有多种冠状动脉粥样硬化的危险因素,包括糖尿病、高血压和高脂血症。本病例强调了结节病在病因不明的复发性典型胸痛患者鉴别诊断中的重要性。
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