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首页> 外文期刊>European Heart Journal - Case Reports >Double trouble – thyro-pericarditis: rare presentation of Graves’ disease as pericarditis—a case report
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Double trouble – thyro-pericarditis: rare presentation of Graves’ disease as pericarditis—a case report

机译:双重麻烦 - 甲状腺炎:稀有坟墓疾病的罕见呈现 - 案例报告

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Background Acute pericarditis is frequently encountered in clinical practice; however, pericarditis as the first presentation of Graves' disease is rare and mainly limited to case reports in the literature. We hereby report a case in which a young patient presented with pericarditis as the first manifestation of Graves’ disease. Case summary A 24-year-old male was admitted to hospital with presenting complaint of left-sided chest pain, gradual in onset, 6/10 in intensity, sharp in character, increased by deep breathing and improved by leaning forward. Patient also gave a history of insomnia, unintentional weight loss despite a good appetite, heat intolerance, and anxiety. On clinical examination, the patient had features of thyrotoxicosis, i.e., tachycardia, high volume pulse, and sweaty palms with fine tremors. There was no associated pericardial rub. Neck examination shows diffuse, non-tender goitre. Electrocardiogram findings were consistent with acute pericarditis. His thyroid function tests demonstrated hyperthyroidism and anti-thyroglobulin antibodies were also significantly elevated. Echocardiogram showed preserved left ventricular systolic function and a small global pericardial effusion without any signs of tamponade. He was diagnosed with Graves’ disease revealing itself as pericarditis and was started on ibuprofen, beta-blockers, and carbimazole. Patient had marked clinical and biochemical improvement on 3 monthly follow-ups. Discussion Thyro-pericarditis is a rare entity, and limited literature is available regarding this combination. The exact aetiology of Graves associated pericarditis is unknown. There is a possibility of interaction of autoantibodies with receptors on pericardium. Diagnosis is based on a detailed history, clinical examination, supplemented by relevant investigations (elevated free T4 and thyroid receptor antibodies, suppressed thyroid stimulating hormone (TSH) and Imaging via ultrasound). Mainstay of treatment includes non-steroidal anti-inflammatory drugs, beta-blockers, and anti-thyroidal medications.
机译:背景技术在临床实践中经常遇到急性心包炎;然而,心包炎作为坟墓疾病的第一次介绍是罕见的,主要限于文献中的病例报告。我们特此举报了一种案例,其中一名患有心包炎作为坟墓疾病的第一个表现形式的患者。案例摘要一名24岁的男性被录取为医院,提出左侧胸痛的抱怨,逐渐发作,6/10强度,性格剧烈,深呼吸的深呼吸,通过向前倾斜而提高。患者还给出了失眠的历史,尽管有很好的食欲,热不耐受和焦虑,但仍然存在无意的体重减轻。在临床检查上,患者具有甲状腺酸的特征,即心动过速,高体积脉冲和具有良好震颤的汗水棕榈树。没有相关的心包摩擦。颈部检查显示弥漫性,非嫩的GoItre。心电图结果与急性心包炎一致。他的甲状腺功能测试显示甲状腺功能亢进和抗甲状腺蛋白抗体也显着升高。超声心动图显示保存的左心室收缩功能和小的全球心包积液,没有任何局部局部的局部迹象。他被诊断出患有坟墓的疾病,将自己视为心包炎,并于布洛芬,β-窝囊和肉甲唑上开始。患者在3个月随访中标志着临床和生化改善。讨论甲型 - 心包炎是一种罕见的实体,有限的文献可用于这种组合。相关心膜炎的坟墓的确切性病是未知的。自身抗体与心包上受体的相互作用的可能性。诊断基于详细的历史,临床检查,通过相关研究补充(升高的T4和甲状腺受体抗体,抑制甲状腺刺激激素(TSH)和通过超声成像)。护理的主要抗原包括非甾体类抗炎药,β-阻滞剂和抗甲状腺药物。

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