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Long segment congenital tracheal stenosis in twins successfully treated by slide tracheoplasty.

机译:双胎长段先天性气管狭窄通过滑行气管成形术成功治疗。

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摘要

Long segment congenital tracheal stenosis (LSCTS), associated with complete tracheal rings, is a rare condition, difficult to manage and historically associated with high mortality rate. We report two pairs of identical twins all affected by LSCTS successfully treated by sliding tracheoplasty. All had severe respiratory distress. Three infants had left pulmonary artery (LPA) sling and one intra-cardiac malformation. Slide tracheoplasty was done under cardiopulmonary bypass, and cardiovascular malformations were corrected at the same time. One child needed plication of paralyzed right hemi-diaphragm and another distal tracheal Palmaz stent insertion due severe tracheobronchomalacia. All children are doing well during 6 months follow-up. Slide tracheoplasty seems to produce the same good early results in twins as for singletons with LSCTS.
机译:长段性先天性气管狭窄(LSCTS)与完整的气管环相关,是一种罕见病,难于管理并且历史上与高死亡率相关。我们报告了两对同卵双胞胎,均受滑行气管成形术成功治疗的LSCTS影响。全部患有严重的呼吸窘迫。 3例婴儿有左肺动脉吊带和1例心脏内畸形。在体外循环下进行滑膜气管成形术,同时纠正了心血管畸形。一个孩子因严重的气管支气管软化症而需要使瘫痪的右半-膜折叠,并需要插入另一个远端的气管Palmaz支架。在6个月的随访中,所有儿童的状况都很好。滑动气管成形术似乎在双胎中产生了与单胎LSCTS相同的早期良好效果。

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