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Congenital emphysema in children: Segmental lung resection as an alternative to lobectomy

机译:小儿先天性肺气肿:肺段切除术可替代肺叶切除术

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Background Congenital emphysema is a rare lung malformation characterized by overinflation of lung segments or lobe, together with ventilation and lung perfusion disorders. The lesion frequently causes respiratory distress in infants and may require urgent surgery. The pathogenesis is still controversial, and the usual treatment recommended is a lobectomy. Aim The aims of the study were to clarify the pathogenesis and relationship to vascular abnormalities and to assess the safety and efficacy of lung-sparing segmental resections. Materials and Methods Retrospective review of hospital records, chest radiograph, digital subtraction angiography, and contrast-enhanced chest CT were used for diagnosis. Results Forty-three (median age 4 months, range 10 days to 10 years) children were diagnosed with congenital emphysema. Most were 1 year of age at presentation (n = 33; 77%). The predominant side affected was the left (n = 24; 56%), and of these all but one had segmental (not lobar) lesions. Most of these then underwent segmental lung resection (S1-S 3) with preservation of the uninvolved lingual (S4-5) segments preserved. A standard lobectomy was used in right-sided lesions. There was a high incidence of vascular abnormalities in association with the emphysematous segments, which may be important in its etiology. One child, referred in extremis and died before surgery could be undertaken. Otherwise, early and late results of surgery were rated as good or excellent in all patients. Longer-term follow-up of the preserved left lingual segments did not suggest any recurrence of emphysema. Conclusion Segmental resection in cases of left-sided congenital emphysema appears effective and merits further use as a lung-sparing operation. ? 2013 Elsevier Inc.
机译:背景先天性肺气肿是一种罕见的肺畸形,其特征是肺节或肺叶过度膨胀,以及通气和肺灌注障碍。病变经常导致婴儿呼吸窘迫,可能需要紧急手术。发病机理仍存在争议,通常推荐的治疗方法是肺叶切除术。目的该研究的目的是阐明发病机理及其与血管异常的关系,并评估保肺节段切除术的安全性和有效性。材料和方法回顾性分析医院的病历,胸部X光片,数字减影血管造影和对比增强的胸部CT进行诊断。结果43例(中位年龄为4个月,范围为10天至10岁)被诊断为先天性肺气肿。大多数患者在出诊时均小于1岁(n = 33; 77%)。受影响的主要一侧是左侧(n = 24; 56%),除一个以外,所有这些患者均具有节段性(非大叶性)病变。然后对大多数这些患者进行节段性肺切除术(S1-S 3),并保留未累及的舌侧节段(S4-5)。右侧病变使用标准的肺叶切除术。与气肿部位相关的血管异常发生率很高,这可能在其病因学中很重要。一名被送往极端的儿童在手术之前死亡。否则,在所有患者中,手术的早期和晚期结果均被评为良好或优异。对保留的左舌段进行长期随访未发现任何肺气肿复发。结论左侧先天性肺气肿的节段切除术似乎是有效的,值得进一步用于保肺手术。 ? 2013爱思唯尔公司

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