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[一名患有唐氏综合征的青少年出现伴有低钾血症和甲状腺功能亢进的肌无力]

[Muscle weakness with hypokalemia and hyperthyroidism in an adolescent with Down syndrome].

作者信息

Florio Selene, Mattone María C, Gazek Natalia, Belgorosky Alicia, Herzovich Viviana, Dujovne Noelia

机构信息

Servicio de Endocrinología, Hospital de Pediatría "Prof. Dr. Juan P. Garrahan", Buenos Aires, Argentina.

出版信息

Arch Argent Pediatr. 2019 Feb 1;117(1):e37-e40. doi: 10.5546/aap.2019.e37.

Abstract

Acute hypokalemic paralysis is a rare cause of acute weakness. Thyrotoxic periodic paralysis (TPP) is an unusual complication of hyperthyroidism. It is characterized by sudden onset of hypokalemia condition resulting from a shift of potassium into cells and paralysis that primarily affects the lower extremities. Failure to recognize TPP may lead to improper management. Treatment of TPP includes replacing potassium rapidly, using nonselective beta-blockers and correcting the underlying hyperthyroidism as soon as possible. TPP is curable once euthyroid state is achieved. We describe a 13-year-old male with Down syndrome who presented with acute onset of lower extremity weakness secondary to acute hypokalemia and was found to have new onset Graves' disease.

摘要

急性低钾性麻痹是急性肌无力的罕见病因。甲状腺毒症性周期性麻痹(TPP)是甲状腺功能亢进症的一种不寻常并发症。其特征为钾离子向细胞内转移导致低钾血症突然发作,以及主要影响下肢的麻痹。未能识别TPP可能导致治疗不当。TPP的治疗包括迅速补钾、使用非选择性β受体阻滞剂以及尽快纠正潜在的甲状腺功能亢进症。一旦达到甲状腺功能正常状态,TPP是可治愈的。我们报道一名13岁患有唐氏综合征的男性,因急性低钾血症继发急性下肢无力就诊,被发现患有新发的格雷夫斯病。

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