先天性胸廓疾病的外科治疗:15年的中心经验

Catarina Pereira Moita, Catarina Figueiredo, Zenito Cruz, João Maciel, Ana Rita Costa, João Santos Silva, João Eurico Reis, Paulo Calvinho
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引用次数: 0

摘要

简介先天性胸廓疾病代表了一系列胎儿肺芽发育异常,可能会影响呼吸能力和生活质量。我们旨在评估手术治疗 4 种主要先天性疾病的影响:我们对 2007 年至 2022 年期间在我们的三级医疗中心接受手术治疗的患者进行了回顾性队列分析:在这 15 年间,我们共治疗了 33 名患者,其中男性占 55%。22名患者(67%)无症状。有症状时,最常见的临床表现是呼吸道感染复发(18%)。13名患者(39%)是通过胎儿超声波检查确诊的。这项研究包括13例肺动脉栓塞患者(39%)、11例支气管源性囊肿患者(33%)、7例先天性肺气道畸形患者(21%)和2例先天性肺叶气肿患者(6%)。仅考虑肺部畸形情况,我们就收治了 22 名患者,中位年龄为 3 [1-67] 岁。手术包括双叶切除术(9%)、肺叶切除术(77%)、肺叶切除加楔形切除术(5%)、肺段切除术(5%)和楔形切除术(5%)。关于支气管源性囊肿,我们共治疗了 11 例患者,中位年龄为 19 [14-66] 岁。我们发现了 1 例肺门、1 例肺内和 9 例纵隔病变,其中 4 例为食道旁、4 例为心包下、1 例为其他病变。总体而言,61%的患者采用开胸手术,33%采用VATS,6%采用RATS。中位引流时间为 3 [1-40] 天,中位住院时间为 4 [1-41] 天。没有死亡病例。最后,94%的患者术后临床症状有所改善:结论:随着成像技术和产前筛查的改进,先天性胸廓畸形的早期诊断率大大提高。治疗可包括预期保守治疗。然而,在特定病例中,手术在控制症状和预防疾病进展方面可能发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surgical Management Of Congenital Thoracic Disorders: A 15-Year Center Experience.

Introduction: Congenital thoracic disorders represent a spectrum of fetal lung bud development abnormalities, which may affect breathing capacity and quality of life. We aim to evaluate the impact of surgery in the treatment of 4 major congenital conditions.

Materials and methods: We performed a retrospective cohort analysis of patients who underwent surgical treatment in our tertiary center, from 2007 to 2022.

Results: Over the 15-year period, we treated 33 patients, with a male predominance of 55%. 22 patients (67%) were asymptomatic. When symptomatic, the recurrence of respiratory infections was the most common clinical presentation (18%). In 13 patients (39%), diagnosis was achieved through fetal ultrasonography. This study encompassed 13 patients with pulmonary sequestration (39%), 11 patients with bronchogenic cysts (33%), 7 patients with congenital pulmonary airway malformation (21%) and 2 patients with congenital lobar emphysema (6%). Considering solely lung malformation conditions, we accounted 22 patients with a median age of 3 [1-67] years-old. Surgery comprised bilobectomy (9%), lobectomy (77%), lobectomy with wedge resection (5%), segmentectomy (5%) and wedge resection (5%). Concerning bronchogenic cysts, we treated 11 patients with a median age of 19 [14-66] years-old. We identified 1 hilar, 1 intrapulmonary and 9 mediastinal lesions, of which 4 were paraesophageal, 4 were subcarinal and 1 was miscellaneous. Overall, surgery was conducted by thoracotomy in 61% of patients, VATS in 33% and RATS in 6%. The median drainage time was 3 [1-40] days and median hospital stay was 4 [1-41] days. There were no cases of mortality. Ensuing, 94% of patients experienced clinical improvement after surgery.

Conclusion: Early diagnosis of congenital thoracic malformations increased considerably with the improvement in imaging technology and prenatal screening. Treatment may include expectant conservative treatment. However, in selected cases, surgery may play an important role in symptomatic control and prevention of disease progression.

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