Hamad Abdel-Mohsen, Elmistekawy Elsayed, Elatafy Elatafy
Department of Cardiothoracic Surgery, University of Tanta, Tanta, Egypt.
Interact Cardiovasc Thorac Surg. 2012 Oct;15(4):618-21. doi: 10.1093/icvts/ivs305. Epub 2012 Jul 2.
Middle lobe syndrome is a well-known clinical condition. In this retrospective study, we report our experience with a similar clinicopathological condition affecting the left lower lobe.
The data of 17 patients with atelectasis or bronchiectasis of the left lower lobe who underwent lobectomy during the period from January 2000 to December 2011 were reviewed. Demographic, clinical, radiological and surgical data were collected.
Seventeen patients were included in this study, only one adult male patient of 52 years and 16 children. The paediatric patients were 10 boys and 6 girls, their age ranged from 2 to 11 years, mean 6.19 ± 2.6 years. Most patients presented with recurrent respiratory infection 15/17 (88.2%). The lag time before referral to surgery ranged from 3 to 48 months, mean 17.59 ± 13.1 months. Radiological signs of bronchiectasis were found in 11 (64.7%) patients. Bronchoscopy showed patent lower lobe bronchus in all patients. The criteria for lobectomy were evidence of bronchiectasis [11 (64.71%) patients], persistent atelectasis of the lobe after bronchoscopy and intensive medical therapy for a maximum of 2 months [6 (35.29%) patients]. Histopathological examination showed bronchiectasis in 11 (64.71%) patients, fibrosing pneumonitis in 4 (23.53%) patients and peribronchial inflammation in 2 (11.76%) patients. Most patients were doing well 1 year after surgery.
Chronic atelectasis of the left lower lobe is a clinicopathological condition equivalent to middle lobe syndrome. Impaired collateral ventilation together with airway plugging with secretion is an accepted explanation. Surgical resection is indicated for bronchiectatic lobe or failure of 2-month intensive medical therapy to resolve lobar atelectasis.
中叶综合征是一种众所周知的临床病症。在这项回顾性研究中,我们报告了我们对影响左肺下叶的类似临床病理状况的经验。
回顾了2000年1月至2011年12月期间接受肺叶切除术的17例左肺下叶肺不张或支气管扩张患者的数据。收集了人口统计学、临床、放射学和手术数据。
本研究纳入17例患者,仅1例52岁成年男性患者,其余16例为儿童。儿科患者中10例为男孩,6例为女孩,年龄范围为2至11岁,平均6.19±2.6岁。大多数患者出现反复呼吸道感染15/17(88.2%)。转诊至手术前的延迟时间为3至48个月,平均17.59±13.1个月。11例(64.7%)患者发现支气管扩张的放射学征象。支气管镜检查显示所有患者的下叶支气管通畅。肺叶切除术的标准为支气管扩张的证据[11例(64.71%)患者]、支气管镜检查及强化药物治疗最多2个月后肺叶持续肺不张[6例(35.29%)患者]。组织病理学检查显示11例(64.71%)患者为支气管扩张,4例(23.53%)患者为纤维性肺炎,2例(11.76%)患者为支气管周围炎症。大多数患者术后1年情况良好。
左肺下叶慢性肺不张是一种与中叶综合征相当的临床病理状况。侧支通气受损以及分泌物阻塞气道是一种公认的解释。对于支气管扩张的肺叶或强化药物治疗2个月未能解决肺叶肺不张的情况,建议进行手术切除。