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患有三尖瓣闭锁和大动脉转位的新生儿的全身灌注不足。与左心发育不全综合征相似。

Systemic hypoperfusion in a neonate with tricuspid atresia and transposition of the great arteries. Similarity to the hypoplastic left heart syndrome.

作者信息

Folger G M

出版信息

Angiology. 1980 Oct;31(10):721-4. doi: 10.1177/000331978003101009.

Abstract

Infants with the hypoplastic left heart syndrome present a reproducible appearance that terminates in irreversible shock during the neonatal period. There is disagreement over the exact cause of this appearance. This case involves a newborn infant with tricuspid atresia and transposition of the great arteries, and with the clinical appearance and course usually reserved for neonates with the hypoplastic left heart syndrome. Accurate diagnosis is crucial in all such infants to correctly distinguish those with a hopeless outcome from those amenable to palliative cardiovascular surgery. This case supports the contention that ductal closure alone is not the principal cause of death in infants with hypoplastic left heart syndrome.

摘要

患有左心发育不全综合征的婴儿呈现出一种可重复出现的表现,在新生儿期最终会发展为不可逆的休克。对于这种表现的确切原因存在分歧。该病例涉及一名患有三尖瓣闭锁和大动脉转位的新生儿,其临床表现和病程通常见于患有左心发育不全综合征的新生儿。准确诊断对于所有此类婴儿至关重要,以便正确区分那些预后无望的婴儿和适合进行姑息性心血管手术的婴儿。该病例支持了这样一种观点,即单纯动脉导管闭合并非左心发育不全综合征婴儿死亡的主要原因。

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