Lee Sungkwang, Kim Do Hyung, Lee Sang Kwon
Department of Clinical Korean Medicine, Graduate School, Kyung Hee University, Kyungheedae-ro, Dongdaemun-gu, Seoul, Republic of Korea.
Department of Acupuncture and Moxibustion, Kyung Hee University Korean Medicine Hospital, Kyungheedae-ro, Dongdaemun-gu, Seoul, Republic of Korea.
Interact Cardiovasc Thorac Surg. 2017 Mar 1;24(3):425-429. doi: 10.1093/icvts/ivw408.
Lung segmental resection is a better treatment option than lobectomy for patients with prenatally diagnosed congenital lung malformations (CLMs). However, data are lacking on the effects of this procedure in prenatally diagnosed CLM patients. In this study, we explored whether parenchyma-saving resection was feasible in patients with this condition.
A retrospective analysis was performed on 27 patients prenatally diagnosed with CLM, who subsequently underwent surgery between March 2011 and September 2015. Lobectomies and segmental resections were performed in 7 and 20 patients, respectively, based on the extent of cystic lesion invasion.
The operative time significantly differed between the two groups (lobectomy group, 92.9 ± 32.0 min; segmental resection group, 126.5 ± 37.5 min). However, the duration of chest tube drainage and the length of hospital stay did not significantly differ between the groups. Chest computed tomography (CT) was performed during follow-up on all but 3 patients. We encountered 2 cases of remnant lesions, and one instance of a small emphysematous lesion around the surgical site was noted in either group.
Lung-sparing surgery is relatively safe with few complications. In this study, the incidence of remnant lung lesions (a drawback of segmentectomy) was low. Thus, segmental resection affords results similar to those of lobectomy in patients with prenatally diagnosed CLM. Furthermore, segmental resection can preserve lung volume, thereby maintaining later pulmonary function. Therefore, elective segmental resection performed after precise identification of the lesions' locations may be highly beneficial for CLM patients.
对于产前诊断为先天性肺发育畸形(CLM)的患者,肺段切除术比肺叶切除术是更好的治疗选择。然而,关于该手术对产前诊断为CLM患者的影响的数据尚缺乏。在本研究中,我们探讨了实质保留切除术在这类患者中是否可行。
对27例产前诊断为CLM且随后于2011年3月至2015年9月期间接受手术的患者进行回顾性分析。根据囊性病变侵犯范围,分别对7例患者实施了肺叶切除术,对20例患者实施了肺段切除术。
两组手术时间有显著差异(肺叶切除术组,92.9±32.0分钟;肺段切除术组,126.5±37.5分钟)。然而,两组胸腔闭式引流时间和住院时间无显著差异。除3例患者外,所有患者在随访期间均进行了胸部计算机断层扫描(CT)。我们遇到2例残留病变,两组中均有1例在手术部位周围发现小的气肿性病变。
保留肺组织的手术相对安全,并发症较少。在本研究中,残留肺病变(肺段切除术的一个缺点)的发生率较低。因此,肺段切除术在产前诊断为CLM的患者中所获得的结果与肺叶切除术相似。此外,肺段切除术可以保留肺容积,从而维持后期肺功能。因此,在精确确定病变位置后进行选择性肺段切除术可能对CLM患者非常有益。