Suppr超能文献

产前检测出的先天性肺气道畸形:牛津大学的经验

Antenatally Detected Congenital Pulmonary Airway Malformations: The Oxford Experience.

作者信息

Thakkar Hemanshoo Sudhir, Durell Jonathan, Chakraborty Subhasis, Tingle Bianca-Lea, Choi Arnwald, Fowler Darren J, Gould Steve J, Impey Lawrence, Lakhoo Kokila

机构信息

Department of Paediatric Surgery, John Radcliffe Hospital, Children's Hospital Headley Way, Oxford, Oxford, Oxfordshire, United Kingdom.

Department of Paediatric Radiology, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

出版信息

Eur J Pediatr Surg. 2017 Aug;27(4):324-329. doi: 10.1055/s-0036-1593379. Epub 2016 Oct 10.

Abstract

Congenital airway pulmonary malformations are increasingly being diagnosed, but their management continues to remain controversial. Our approach has been to offer surgery to mitigate the risk of infection and possible malignancy. All patients routinely undergo a CT scan of the chest postnatally and once the diagnosis is confirmed, minimal access surgery is offered. Our anesthetists provide single-lung ventilation to enhance the operative view. We conducted a retrospective review over a 10-year period, during which 91 patients were prenatally suspected to have a cystic lung lesion. There were 88 live births of which 29 (33%) cases were initially managed conservatively based on CT findings. Five of these patients, however, became symptomatic needing surgery. A total of 64 (73%) patients underwent surgery with the most common lesions being congenital pulmonary airway malformations (CPAMs) (24), hybrid lesions (19), and pulmonary sequestrations (12). The median age at surgery was 5 months (1 day to 17 months). Using a minimal access approach, 41 (64%) cases were completed with 17 performed open from the onset. Open surgery was indicated in neonates who became symptomatic within the first few weeks of life as well as patients in respiratory distress that would not tolerate either single-lung ventilation or gas insufflation. There were six further conversions to open from minimal access surgery due to poor visualization or technical difficulties. One patient needed a perioperative blood transfusion and one patient had a more prolonged stay due to persistent air leak managed conservatively. Among asymptomatic patients, evidence of microscopic disease was seen, which included infection as well as two cases of tumors, one pleuropulmonary blastoma seen as part of a CPAM, and one rhabdomyomatous dysplasia seen in the CPAM component of a hybrid lesion. In our experience, excising asymptomatic lesions is safe with minimal complications. Single-lung ventilation in combination with thoracoscopy provides excellent vision. There is a risk of infection and a definite, albeit low, risk of malignancy, which may outweigh the benefits of conservative management.

摘要

先天性气道肺畸形的诊断越来越多,但对其治疗仍存在争议。我们的方法是进行手术以降低感染和可能发生恶性肿瘤的风险。所有患者出生后常规进行胸部CT扫描,一旦确诊,即提供微创手术。我们的麻醉师提供单肺通气以改善手术视野。我们进行了一项为期10年的回顾性研究,在此期间,91例患者在产前被怀疑患有肺囊性病变。共有88例活产,其中29例(33%)最初根据CT结果进行保守治疗。然而,这些患者中有5例出现症状需要手术。共有64例(73%)患者接受了手术,最常见的病变为先天性肺气道畸形(CPAM)(24例)、混合型病变(19例)和肺隔离症(12例)。手术的中位年龄为5个月(1天至17个月)。采用微创手术方法,41例(64%)手术完成,17例一开始就进行了开放手术。对于出生后几周内出现症状的新生儿以及不能耐受单肺通气或气体注入的呼吸窘迫患者,需进行开放手术。由于视野不佳或技术困难,另有6例从微创手术转为开放手术。1例患者围手术期需要输血,1例患者因持续漏气保守治疗而住院时间延长。在无症状患者中,发现了微观疾病的证据,包括感染以及2例肿瘤,1例胸膜肺母细胞瘤见于CPAM,1例横纹肌瘤样发育异常见于混合型病变的CPAM成分。根据我们的经验,切除无症状病变是安全的,并发症极少。单肺通气联合胸腔镜提供了极佳的视野。存在感染风险以及明确的、尽管很低的恶性肿瘤风险,这可能超过保守治疗的益处。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验