大动脉d型转位合并气管支气管软化症中的双主动脉弓。
Double aortic arch in d-transposition of the great arteries complicated by tracheobronchomalacia.
作者信息
Tůma S, Slavík Z, Tax P, Hucin B, Skovránek J
机构信息
Clinic for Imaging Methods, University Hospital Motol, Prague, Czech Republic.
出版信息
Cardiovasc Intervent Radiol. 1995 Mar-Apr;18(2):115-7. doi: 10.1007/BF02807235.
PMID:7773993
Abstract
Simultaneous occurrence of d-transposition of the great arteries and aortic arch malformations is very rare. A case of this malformation, the fourth case reported in the literature, is described. Despite successful surgery, tracheobronchomalacia was fatal at the age of 7 months.
摘要
大动脉d-转位与主动脉弓畸形同时出现的情况非常罕见。本文描述了这样一例畸形病例，这是文献报道的第四例。尽管手术成功，但气管软化症在患儿7个月大时导致了死亡。
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