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甲状腺功能亢进症:可逆性肺动脉高压的罕见病因。

Hyperthyroidism: a rare cause of reversible pulmonary hypertension.

作者信息

Wasseem Rock, Mazen Elias, Walid Saliba R

机构信息

Department of Internal Medicine C, Hae'meK Medical Center, Afula 18101, Israel.

出版信息

Am J Med Sci. 2006 Sep;332(3):140-1. doi: 10.1097/00000441-200609000-00009.

Abstract

We describe a case of pulmonary hypertension and high-output heart failure in a 61-year-old woman suffering from relapsing Graves disease. The patient experienced prompt hemodynamic and symptomatic recovery after normal thyroid function was restored. Possible mechanisms for the development of pulmonary arterial hypertension due to hyperthyroidism include damage to pulmonary vascular endothelium due to high cardiac output or an autoimmune process or increased metabolism of intrinsic pulmonary vasodilators. Another possible mechanism is vascular vasoconstriction due to decreased cholinergic output.

摘要

我们描述了一例61岁患有复发性格雷夫斯病的女性患者出现肺动脉高压和高输出量心力衰竭的病例。在甲状腺功能恢复正常后,患者的血流动力学和症状迅速恢复。甲状腺功能亢进导致肺动脉高压发展的可能机制包括高心输出量对肺血管内皮的损伤、自身免疫过程或肺内源性血管扩张剂代谢增加。另一种可能机制是胆碱能输出减少导致的血管收缩。

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