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一名终末期肾病患者急性心肌梗死后铁蛋白水平极高。

Extremely high ferritin level after an acute myocardial infarction in an end stage renal disease patient.

作者信息

Sandhu Gagangeet, Mankal Pavan, Gupta Isha, Tagani Adrian, Ranade Aditi, Jones James, Bansal Anip

出版信息

Clin Nephrol. 2014 Jul;82(1):68-72. doi: 10.5414/CN107696.

Abstract

We present here a case of an asymptomatic end-stage renal disease (ESRD) patient, who had an unexplained persistent mild leukocytosis in the setting of an extremely high ferritin level (8,997 ng/ml; reference range: 12 - 300 ng/ml) 3 weeks after she suffered from a myocardial infarction (MI). Infection as the cause of these laboratory abnormalities was ruled out. A week later, the patient was noted to have asymptomatic hypotension (100/60 mmHg; her baseline blood pressure was 120/70 mmHg) during a maintenance hemodialysis session. An echocardiography revealed an interval development of moderate pericardial effusion when compared to her previous echocardiography 4 weeks before. In the setting of a recent MI with other laboratory markers suggesting an ongoing inflammatory process, a tentative diagnosis of Dressler's syndrome was made. A pericardial tap yielded exudative (bloody) fluid, thus, confirming our suspicion. Dressler's syndrome results from an inflammation of the pericardium as a consequence of an underlying autoimmune process few weeks to months after a myocardial infarction or post-cardiac surgery. Although it typically presents with pleuritic chest pain, fever, leukocytosis, and a friction rub; our case illustrates that the initial presentation may be asymptomatic in ESRD patients. For the same reason, it is likely an under-recognized entity in such patients. An unexplained elevated ferritin in an ESRD patient with recent history of MI should prompt an investigation for Dressler's syndrome. In those with associated significant pericardial effusion, daily HD should be initiated and anticoagulation should be avoided. Unlike other ESRD associated pericarditis, steroids and NSAIDs should be avoided in Dressler's syndrome as they may hamper cardiac remodeling in the immediate post-MI period. Colchicine may offer some benefit in patients with associated chest pain. For those failing medical management or manifesting overt signs of tamponade, surgical drainage should be preferred.

摘要

我们在此报告一例无症状终末期肾病(ESRD)患者,该患者在心肌梗死(MI)3周后出现极高的铁蛋白水平(8997 ng/ml;参考范围:12 - 300 ng/ml),同时伴有无法解释的持续性轻度白细胞增多。感染作为这些实验室异常的原因被排除。一周后,该患者在维持性血液透析期间被发现有无症状性低血压(100/60 mmHg;其基础血压为120/70 mmHg)。超声心动图显示与4周前的上一次超声心动图相比,出现了中度心包积液。在近期发生心肌梗死且其他实验室指标提示存在持续炎症过程的情况下,初步诊断为 Dressler 综合征。心包穿刺抽出了渗出性(血性)液体,从而证实了我们的怀疑。Dressler 综合征是心肌梗死或心脏手术后数周至数月由于潜在的自身免疫过程导致心包炎症引起的。虽然它通常表现为胸膜炎性胸痛、发热、白细胞增多和摩擦音;但我们的病例表明,在 ESRD 患者中初始表现可能是无症状的。出于同样的原因,它在这类患者中可能是一个未被充分认识的疾病。近期有心肌梗死病史的 ESRD 患者中,不明原因的铁蛋白升高应促使对 Dressler 综合征进行调查。对于伴有大量心包积液的患者,应开始每日血液透析并避免抗凝。与其他 ESRD 相关的心包炎不同,Dressler 综合征应避免使用类固醇和非甾体抗炎药,因为它们可能在心肌梗死后即刻妨碍心脏重塑。秋水仙碱可能对伴有胸痛的患者有一定益处。对于药物治疗无效或出现明显心包填塞体征的患者,应首选手术引流。

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