Imaging clinical case

C. Liz, S. Lira, S. Teixeira
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Abstract

3000 children. They are mostly of congenital origin and the left hemithorax is most commonly affected. Acquired diaphragmatic hernias are rare and mainly traumatic or iatrogenic. The case of a 16-year-old adolescent with cerebral palsy submitted to scoliosis surgical correction five months earlier is presented. The girl was brought to the emergency department due to dyspnea and vomiting of acute onset. At physical examination, she was agitated and presented with skin pallor, polypnea, and suprasternal and subcostal retraction. Pulmonary breath sounds in the left hemithorax were absent. The girl maintained blood oxygen saturation levels of 90% with 2 L/ min of O2 and was hemodynamically stable. The x-ray showed the gastric bubble in the left hemithorax, leading to the diagnosis. This case shows the clinical challenge posed by children with children with cerebral palsy, who are unable to define their symptoms and make clinical state difficult to access. Repair of neuromuscular scoliosis has higher complication rates than congenital or idiopathic scoliosis. Diaphragmatic hernia is an uncommon complication, with only few cases described in the literature.
影像学临床病例
3000名儿童。他们大多是先天性的起源和左半胸最常见的影响。获得性膈疝是罕见的,主要是外伤性或医源性。一个16岁的青少年与脑瘫提交脊柱侧凸手术矫正五个月前提出的情况。该女童因急性发作的呼吸困难和呕吐被送至急诊科。体格检查时,患者情绪激动,皮肤苍白,呼吸急促,胸骨上和肋下收缩。左半胸无肺呼吸音。女孩血氧饱和度维持在90%,2升/分钟,血流动力学稳定。x光片显示左半胸有胃泡,从而确诊。这个病例显示了脑瘫患儿的临床挑战,他们无法确定自己的症状,使临床状态难以获得。神经肌肉性脊柱侧凸的修复比先天性或特发性脊柱侧凸有更高的并发症发生率。膈疝是一种罕见的并发症,在文献中只有少数病例被描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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