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新生儿格雷夫斯病中的可逆性肺动脉高压。

Reversible pulmonary hypertension in neonatal Graves disease.

作者信息

O'Donovan D, McMahon C, Costigan C, Oslizlok P, Duff D

机构信息

Department of Cardiology, Our Lady's Hospital for Sick Children, Dublin, Ireland.

出版信息

Ir Med J. 1997 Jun-Jul;90(4):147-8.

PMID:9267095
Abstract

Neonatal thyrotoxicosis may occur by transplacental transfer of thyroid stimulating immunoglobins from the mother. Although the clinical manifestations may vary in the new-born period, hyperthyroidism has been associated with several cardiac complications including supraventricular tachycardia, cardiomyopathy and congestive cardiac failure. We report the case of a nine day old baby who presented with severe pulmonary hypertension in association with congestive cardiac failure secondary to neonatal thyrotoxicosis. Treatment of the heart failure and restoration of the thyroid function resulted in complete regression of the pulmonary hypertension. The recognition and reversibility of pulmonary hypertension in neonatal Graves disease has not been previously described.

摘要

新生儿甲状腺毒症可能因母体甲状腺刺激免疫球蛋白经胎盘转移而发生。尽管新生儿期的临床表现可能有所不同,但甲状腺功能亢进与多种心脏并发症有关,包括室上性心动过速、心肌病和充血性心力衰竭。我们报告一例9天大的婴儿,该婴儿因新生儿甲状腺毒症继发充血性心力衰竭而出现严重肺动脉高压。心力衰竭的治疗和甲状腺功能的恢复导致肺动脉高压完全消退。新生儿格雷夫斯病中肺动脉高压的识别及可逆性此前尚未见报道。

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