Perez Pedro E, Sze Wilson, Miller Joshua
AACE Clin Case Rep. 2019 Aug 28;5(5):e307-e310. doi: 10.4158/ACCR-2019-0239. eCollection 2019 Sep-Oct.
To present a unique phenomenon of a patient in addisonian crisis with electrocardiogram (ECG) anomalies that resolved following glucocorticoid therapy.
We present the case report followed by discussion with literature review.
A 25-year-old male with Addison disease (AD) presented with a 1-week history of lightheadedness, shortness of breath, chest pain, abdominal pain, postural hypotension, and tachycardia. The patient was diagnosed with addisonian crisis and started on intravenous, high-dose glucocorticoids. An ECG showed right-heart axis deviation and T-wave inversions. In the context of ongoing chest pain, there was concern for myocardial ischemic attack and the patient underwent an extensive cardiac evaluation. Cardiac workup was negative and an echocardiogram showed an ejection fraction of 50 to 55%. The ECG abnormalities resolved 1 day into his hospital admission and his other symptoms resolved 2 days following treatment with steroids.
AD is a rare, potentially lethal, and commonly misdiagnosed disease often first encountered clinically amidst an incident episode of adrenal crisis. Our AD patient was undergoing an adrenal crisis with ECG changes positive for probable cardiac ischemia. Glucocorticoid deficiency has been previously linked with decreased cardiac function and myocardial ischemia, though the underlying mechanisms are not fully clear. This patient recovered within 2 days after receiving corticosteroid supplementation. There have been similar cases previously reported. In each of these, patients underwent extensive and costly workup to evaluate cardiac function, yet all patients fully recovered with corticosteroids. Understanding the physiology and clinical presentation of adrenal crisis will be useful in establishing an earlier diagnosis, thus preventing mortality and avoiding unnecessary, expensive evaluations.
呈现一名艾迪生病危象患者出现心电图(ECG)异常,而该异常在糖皮质激素治疗后得以缓解这一独特现象。
我们先呈现该病例报告,随后结合文献回顾进行讨论。
一名25岁的艾迪生病(AD)男性患者,有1周的头晕、气短、胸痛、腹痛、体位性低血压和心动过速病史。该患者被诊断为艾迪生病危象,并开始静脉注射大剂量糖皮质激素。心电图显示右心轴偏移和T波倒置。鉴于持续存在的胸痛,担心发生心肌缺血发作,患者接受了全面的心脏评估。心脏检查结果为阴性,超声心动图显示射血分数为50%至55%。入院第1天,心电图异常消失,使用类固醇治疗2天后,他的其他症状也得到缓解。
艾迪生病是一种罕见、潜在致命且常被误诊的疾病,临床上通常在肾上腺危象发作时首次遇到。我们的艾迪生病患者正处于肾上腺危象,心电图改变提示可能存在心脏缺血。既往糖皮质激素缺乏与心脏功能下降和心肌缺血有关,但其潜在机制尚不完全清楚。该患者在接受皮质类固醇补充治疗后2天内康复。此前已有类似病例报道。在每一个病例中,患者都接受了广泛且昂贵的心脏功能评估检查,但所有患者使用皮质类固醇后均完全康复。了解肾上腺危象的生理机制和临床表现,将有助于早期诊断,从而预防死亡并避免不必要的昂贵检查。