先天性叶肺气肿

Pediatría Pub Date : 2020-09-30 DOI:10.14295/RP.V53I3.212
Lizeth Marín Gómez, Juan Salazar
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引用次数: 0

摘要

先天性大叶性肺气肿是一种罕见的肺部畸形,其特征是受影响的肺叶过度膨胀;50%的患者在出生时出现症状,可能与其他症状混淆,如呼吸道感染、肺不张、气胸等。胸片对诊断有用;然而,胸部断层扫描是必要的,以区分它与其他畸形。在大多数情况下,治疗的选择是肺叶切除术,气胸是最常见的并发症。我们提出一个18天的患者急性呼吸道感染和呼吸衰竭的症状,诊断为先天性肺气肿,谁接受肺叶切除术。呼吸道症状可能是先天性肺气肿的首要表现。临床和影像学上的怀疑可以进行早期诊断,避免与肺不张、囊性腺瘤样畸形等其他疾病混淆。
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Enfisema lobar congénito
Congenital lobar emphysema is a rare lung malformation characterized by hyperinflation ofthe lung lobe affected; 50% of patients present symptoms at birth, which can be confused with other entities such as respiratory infections, atelectasis, pneumothorax, among others. Chest radiography is useful for diagnosis; however, a chest tomography is necessary to differentiate it from other malformations. In most cases, the treatment of choice is a lobectomy, and pneumothorax the most frequent complication. We present an 18-day old patient with symptoms of acute respiratory infection and ventilatory failure, diagnosed with congenital lobar emphysema, who underwent lobectomy.Respiratory symptoms may be the first manifestation of congenital lobar emphysema. Its clinical and radiological suspicion can carry out an early diagnosis, avoiding confusion with other entities such as atelectasis and cystic adenomatous malformation.
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