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先天性气管狭窄合并心肺异常:两例报告并文献复习

Congenital tracheal stenosis with associated cardiopulmonary anomalies: report of two cases with a review of the literature.

作者信息

Voland J R, Benirschke K, Saunders B

出版信息

Pediatr Pulmonol. 1986 Jul-Aug;2(4):247-9. doi: 10.1002/ppul.1950020414.

Abstract

We present two infants with congenital tracheal stenosis with complete tracheal rings. Both had associated congenital anomalies. The first case showed cardiac malformations, and the second case had agenesis of the right lung. We review the literature, in particular with reference to tracheal stenosis and pulmonary agenesis. We also propose that the constellation of anomalies may result from defects in the cervical mesenchyme and, as such, may represent one end of a spectrum of cervical mesenchymal field defects.

摘要

我们报告了两名患有先天性气管狭窄且伴有完整气管环的婴儿。两人均伴有先天性异常。第一例表现为心脏畸形,第二例有右肺发育不全。我们回顾了文献,特别是关于气管狭窄和肺发育不全的文献。我们还提出,这些异常的组合可能是由于颈部间充质缺陷所致,因此可能代表了颈部间充质场缺陷谱系的一端。

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