Department of Thoracic and Tumor Surgery, Children's Hospital Affiliated to Shandong University, Jinan, 250022, Shandong, China.
Department of Thoracic and Tumor Surgery, Jinan Children's Hospital, Jinan, 250022, Shandong, China.
BMC Pediatr. 2024 Sep 28;24(1):604. doi: 10.1186/s12887-024-05083-5.
Intra-lobar (ILS) and extra-lobar lung (ELS) sequestrations represent rare congenital lung malformations. Despite their benign nature, the lesions pose risks such as recurrent pulmonary infections, hemoptysis, congestive heart failure, and tumor development. Pulmonary sequestration (PS) typically manifests in two forms, ILS and ELS, with bilateral occurrence being exceptionally rare and mostly requiring bilateral thoracic surgery.
A 9-year-old child, who initially presented with bilateral lung lesions without respiratory symptoms, was diagnosed with PS following a chest computed tomography scan. The surgical approach was determined based on the absence of inflammation and the clear demarcation of the lesions from normal lung tissue, highlighted by a unique tissue connection between the ILS and ELS across the chest cavities. We used a novel method wherein the left ELS was successfully pulled into the right chest cavity and both sequestrations were concurrently resected. Postoperative recovery was smooth, with no complications or residual lesions.
Our findings highlight the importance of thorough preoperative planning with enhanced computed tomography. Simultaneous unilateral thoracoscopic surgery can be a viable, less invasive option for treating bilateral PS, offering benefits such as reduced recovery time and better cosmetic outcomes.
肺叶内(ILS)和肺叶外(ELS)隔离症是罕见的先天性肺畸形。尽管病变性质良性,但仍存在复发性肺部感染、咯血、充血性心力衰竭和肿瘤发展等风险。肺隔离症(PS)通常表现为 ILS 和 ELS 两种形式,双侧发生极为罕见,多需行双侧开胸手术。
一名 9 岁儿童,最初表现为双侧肺部病变,无呼吸系统症状,胸部 CT 扫描后诊断为 PS。根据病变无炎症且与正常肺组织分界清晰的特点,决定采用一种新的手术方法,即通过胸腔内独特的组织连接将左肺ELS 成功拉入右胸腔,并同时切除两个隔离症。术后恢复顺利,无并发症或残留病变。
我们的研究结果强调了术前充分准备和增强 CT 的重要性。对于双侧 PS,同期单侧胸腔镜手术是一种可行的微创选择,可缩短康复时间,美容效果更好。