Abdel-Bary Mohamed, Abdel-Naser Mohamed, Okasha Ahmed, Zaki Mohammed, Abdel-Baseer Khaled
Department of Cardiothoracic Surgery, Qena Faculty of Medicine, South Valley University, Safaga Road, Qena, 83523, Egypt.
Department of Anaesthesia and ICU, Assiut Faculty of Medicine, Assiut University, Assiut, Egypt.
J Cardiothorac Surg. 2020 May 19;15(1):102. doi: 10.1186/s13019-020-01145-8.
Congenital lobar overinflation (CLOI) is one of the most important causes of infantile respiratory distress (RD). We aim to evaluate our experience in CLOI management emphasizing on clinical features, diagnostic modalities, surgery and outcomes.
This is a retrospective study for all CLOI cases undergoing surgical management at Qena University Hospital. Demographic data, clinical data, radiographic findings, surgery and postoperative follow-up were reviewed.
A total of 37 neonates and infants with CLOI were presented to our center between January 2015 and January 2019; their mean age was 111.43 ± 65.19 days and 22 were males. All cases presented with RD; and cyanosis in 19 cases. 15 cases presented with recurrent pneumonia and fever. Diminished breath sounds on the affected side and wheezes were the main clinical findings in 30 and 22 cases respectively. On CXR, emphysema was detected in all cases. A confirmatory CT chest was done for all cases. Left upper lobe was affected in 23 cases, right middle lobe in 7 and right upper lobe in 7 cases. Lobectomy was done in thirty-one cases; their mean age at surgery was 147.58 ± 81.49 days and 19 were males. Postoperative complications were noted in 5 cases and postoperative ventilation was required for 2 of them. No morbidity or mortality was reported. The follow-up duration ranged from 3 months to 1 year and all patients were doing well except one case that lost follow up after 3 months.
CLOI is a rare bronchopulmonary malformation that requires a high index of clinical suspicion, especially in persistent and recurrent infantile RD. CT chest is the most useful diagnostic modality. Early management of CLOI improves outcome and avoid life-threatening complications. Surgical management is the treatment of choice in our center without recorded mortality.
先天性肺叶气肿(CLOI)是婴儿呼吸窘迫(RD)的最重要原因之一。我们旨在评估我们在CLOI管理方面的经验,重点关注临床特征、诊断方式、手术及治疗结果。
这是一项针对在基纳大学医院接受手术治疗的所有CLOI病例的回顾性研究。回顾了人口统计学数据、临床数据、影像学检查结果、手术及术后随访情况。
2015年1月至2019年1月期间,共有37例患有CLOI的新生儿和婴儿被送至我们中心;他们的平均年龄为111.43±65.19天,其中22例为男性。所有病例均表现为呼吸窘迫;19例出现紫绀。15例出现反复肺炎和发热。患侧呼吸音减弱和哮鸣音分别是30例和22例的主要临床发现。胸部X线检查显示,所有病例均存在肺气肿。所有病例均进行了胸部CT检查以确诊。23例累及左上叶,7例累及右中叶,7例累及右上叶。31例接受了肺叶切除术;他们手术时的平均年龄为147.58±81.49天,其中19例为男性。5例出现术后并发症,其中2例需要术后通气。未报告有发病或死亡情况。随访时间为3个月至1年,除1例在3个月后失访外,所有患者情况良好。
CLOI是一种罕见的支气管肺畸形,需要高度的临床怀疑指数,尤其是在持续性和反复性婴儿呼吸窘迫的情况下。胸部CT是最有用的诊断方式。CLOI的早期管理可改善治疗结果并避免危及生命的并发症。手术治疗是我们中心的首选治疗方法,且无死亡记录。