Kratochvíl J, Masopust J, Martínková V, Charvát J
Jednotka intenzivní metabolické péce Interní kliniky 2. Iékarské fakulty UK a FN Motol Praha.
Vnitr Lek. 2008 Nov;54(11):1100-1.
Hypokalemic periodic paralysis (HPP) is a rare disorder characterised by acute, potentially fatal atacks of muscle weakness or paralysis. Massive shift of potassium into cells is caused by elevated levels of insulin and catecholamines in the blood. Hypophosphatemia and hypomagnesemia may be also present. Acidobasic status usually is not impaired. HPP occurs as familiar (caused by ion channels inherited defects) or acquired (in patients with hyperthyroidism). On the basis of two clinical cases we present a review of hypokalemic periodic paralysis in hyperthyroid patients. We discuss patogenesis, clinical and laboratory findings as well as the principles of prevention and treatment of this rare disorder.
低钾性周期性麻痹(HPP)是一种罕见的疾病,其特征为急性、可能致命的肌肉无力或麻痹发作。血液中胰岛素和儿茶酚胺水平升高导致钾大量移入细胞内。也可能存在低磷血症和低镁血症。酸碱状态通常不受损害。HPP可呈家族性(由离子通道遗传缺陷引起)或获得性(见于甲状腺功能亢进患者)。基于两个临床病例,我们对甲状腺功能亢进患者的低钾性周期性麻痹进行了综述。我们讨论了这种罕见疾病的发病机制、临床和实验室检查结果以及预防和治疗原则。