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肺叶保留手术治疗先天性肺畸形。

Sparing-lung surgery for the treatment of congenital lung malformations.

机构信息

Department of Paediatric Surgery, Paediatric Surgery Unit, University of Bologna, Via Massarenti, 11, 40138, Bologna, Italy.

出版信息

J Pediatr Surg. 2013 Jul;48(7):1476-80. doi: 10.1016/j.jpedsurg.2013.02.098.

Abstract

PURPOSE

Congenital lung malformations (CLM) are traditionally treated by pulmonary lobectomy. The foremost indication for surgery is that these lesions predispose to respiratory tract infections and to malignancy. Owing to the improvement of prenatal diagnosis, most patients are operated in a timely manner and prophylactically. In this context, lung-sparing surgery (LS) has gained interest as a lung preservation strategy, especially for asymptomatic patients. In the present study, we evaluated both thoracoscopic and open lung-preserving resections as an alternative to lobectomy for CLM resection.

METHODS

We retrospectively reviewed all patients who underwent lung-sparing resection (segmentectomy and atypical resection) for CLM from 2001 to 2010. Data were collected regarding preoperative diagnostic workup, type of intervention, and follow up.

RESULTS

Fifty-four patients received LS for CLM during the study period. Twenty-six were approached thoracoscopically, with 18 cases requiring open conversion for a complete resection. There were six postoperative complications: three asymptomatic pneumothoraces that resolved without intervention, one tension pneumothorax that required replacement of a drainage catheter, and three instances of intra-operative bleeding requiring blood transfusion. Mean duration of follow-up was 65.2 months. Two patients experienced pneumonia during the follow-up period. A third patient had a cystic lung lesion on postoperative computed tomography (CT) which required a second-look surgery.

CONCLUSIONS

LS for CLM is a safe and effective means of lung parenchymal preservation in pediatric patients. Complication rates are comparable to that of traditional lobectomy. In our experience, this type of lung surgery does not carry a higher risk of residual disease and recurrence if accurately planned in selected patients, i.e., those with small asymptomatic lesions. The complication rate is acceptable and apparently not affected by preoperative symptoms. The thoracoscopic approach is recommended, although open conversion should be advocated to avoid too long operative times.

摘要

目的

先天性肺畸形(CLM)传统上采用肺叶切除术治疗。手术的首要指征是这些病变易导致呼吸道感染和恶性肿瘤。由于产前诊断的改善,大多数患者都能及时进行手术并预防性地进行手术。在这种情况下,肺保留手术(LS)作为一种肺保护策略引起了人们的兴趣,尤其是对于无症状患者。在本研究中,我们评估了胸腔镜和开放式肺保留切除术作为 CLM 切除术的肺叶切除术替代方法。

方法

我们回顾性分析了 2001 年至 2010 年间接受肺保留切除术(节段切除术和非典型切除术)治疗 CLM 的所有患者。收集了有关术前诊断检查、干预类型和随访的数据。

结果

研究期间,54 例患者接受 LS 治疗 CLM。26 例患者采用胸腔镜入路,18 例患者因完全切除需要开胸转换。术后有 6 例并发症:3 例无症状气胸无需干预自行消退,1 例张力性气胸需更换引流导管,3 例术中出血需输血。平均随访时间为 65.2 个月。2 例患者在随访期间发生肺炎。第 3 例患者术后 CT 显示肺囊性病变,需再次手术。

结论

LS 治疗 CLM 是小儿患者保留肺实质的一种安全有效的方法。并发症发生率与传统肺叶切除术相当。根据我们的经验,如果在选定的患者(即无症状小病变患者)中准确计划,这种类型的肺手术不会增加残留疾病和复发的风险。并发症发生率可以接受,显然不受术前症状的影响。推荐采用胸腔镜入路,但应提倡开胸转换以避免手术时间过长。

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