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持续性胎儿循环:新生儿肺动脉高压不断演变的临床和影像学概念。

Persistent fetal circulation: an evolving clinical and radiographic concept of pulmonary hypertension of the newborn.

作者信息

Merten D F, Goetzman B W, Wennberg R P

出版信息

Pediatr Radiol. 1977 Sep 1;6(2):74-80. doi: 10.1007/BF00973526.

Abstract

The roentgenographic presentations of 11 newborn infants with hypoxemia secondary to pulmonary vasospasm and subsequent right-to-left shunting of blood through the foramen ovale and/or ductus arteriosus (persistent fetal circulation) are described (P. F. C. Syndrome). One infant had radiographically normal lungs, while ten had pulmonary parenchymal abnormalities including hyaline membrane disease [4], meconium aspiration syndrome [4], or an ill defined pattern of retained lung fluid [2]. The roentgenographic appearance of the lungs, however, was discordant with the severe hypoxemia observed in most. Heart size was variable but some degree of cardiomegaly was commonly present. Tolazoline, a potent vasodilator, was useful diagnostically and may have resulted in increased survival. An expanded clinical and roentgeonographic concept of the PFC syndrome is suggested.

摘要

本文描述了11例因肺血管痉挛继发低氧血症,继而通过卵圆孔和/或动脉导管出现右向左分流(持续胎儿循环,即P.F.C.综合征)的新生儿的X线表现。1例婴儿肺部X线表现正常,而10例有肺实质异常,包括透明膜病[4例]、胎粪吸入综合征[4例]或肺内液体潴留的不明确影像[2例]。然而,大多数婴儿的肺部X线表现与严重低氧血症不一致。心脏大小不一,但通常存在一定程度的心脏扩大。妥拉唑啉是一种强效血管扩张剂,在诊断上有用,且可能提高了生存率。本文提出了PFC综合征更广泛的临床和X线概念。

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