Department of Thoracic Surgery, Van Training and Research Hospital, Van, Turkey.
Ann Thorac Med. 2012 Jan;7(1):8-11. doi: 10.4103/1817-1737.91554.
Right middle lobe syndrome is a rare entity in children, causing high morbidity. Our experience of these patients including their clinical and laboratory characteristics, indications forsurgical management, postoperative courses, and follow-up results was evaluated.
A retrospective analysis was performed involving 20 children with right middle lobe syndrome who were hospitalized and treated with surgical resection of the right middle lobe in Van Training and Research Hospital and Yüzüncüyil university hospital, Turkey, between January 2002 and January 2011.
The mean age of the patients was 10.5 years (range, 5 to 15 years). Twelve patients were boys and eight were girls. The most frequent symptom was chronic cough (75%). Hemoptysis was present in two (10%) patients. One patient was being treated for asthma. 25% positive cultures were identified among the patients. Streptococcus pneumoniae was the most frequently identified agent in sputum. All patients underwent chest computed tomography. There were bronchiectasis in 11 (55%) patients, atelectasis and bronchiectasis in five (25%) patients, and destroyed lung in four (20%) patients. A narrowed middle lobe bronchus was shown in 15 (75%) patients. Bronchoscopy was performed in 18 (90%) patients. Stenosis due to external compression was seen in 12 (60%) patients, hyperemia and bronchitis in two (10%) patients, granulation tissue in two (10%) patients, and dense secretions in two (10%) patients. A history of doctor-diagnosed tuberculosis was present in two (10%) patients. These patients had completed antituberculous treatment. The patients had been symptomatic for the last 1 to 10 years (mean, 4 years) and had received several medical treatments. All patients (totally 20 patients) underwent right middle lobe resection. In one patient, a bronchial abnormality was found intraoperatively. One patient died on postoperative day 10 due to a brain abscess. Three other patients had postoperative complications (15%). Mean duration of follow-up of the patients was 4.5 years (range, 2 months to 12 years). Seventeen patients were asymptomatic, and two patients had improved.
Children with right middle lobe syndrome unresponsive to medical treatment should undergo early lobe resection to avoid serious complications and the progression of the disease to other segments or lobes.
右中叶综合征在儿童中较为罕见,但发病率较高。我们对这些患者的临床和实验室特征、手术治疗适应证、术后过程和随访结果进行了评估。
对 2002 年 1 月至 2011 年 1 月在土耳其凡培训和研究医院和于则利大学医院接受右中叶切除术治疗的 20 例右中叶综合征患儿的临床资料进行回顾性分析。
患儿平均年龄 10.5 岁(515 岁)。男 12 例,女 8 例。最常见的症状为慢性咳嗽(75%)。2 例(10%)患儿咯血。1 例患儿因哮喘接受治疗。25%的患儿培养阳性。痰中最常见的病原体为肺炎链球菌。所有患儿均行胸部 CT 检查。11 例(55%)患儿存在支气管扩张,5 例(25%)患儿存在肺不张和支气管扩张,4 例(20%)患儿存在肺损毁。15 例(75%)患儿存在中叶支气管狭窄。18 例行支气管镜检查,12 例(60%)患儿存在因外部压迫导致的狭窄,2 例(10%)患儿存在充血和支气管炎,2 例(10%)患儿存在肉芽组织,2 例(10%)患儿存在浓稠分泌物。2 例(10%)患儿曾被诊断为结核病,且已完成抗结核治疗。这些患儿均有症状,时间为 110 年(平均 4 年),且接受过多种药物治疗。所有患儿(共 20 例)均接受了右中叶切除术。1 例患儿术中发现支气管异常。1 例患儿术后第 10 天死于脑脓肿。另有 3 例患儿发生术后并发症(15%)。患儿的平均随访时间为 4.5 年(2 个月~12 年)。17 例患儿无症状,2 例患儿症状改善。
对药物治疗无效的右中叶综合征患儿应行早期肺叶切除术,以避免严重并发症和疾病向其他节段或肺叶进展。