Lu M, Wang M, Zhu X, Chen Y H, Yao W Z
Department of Respiratory Medicine, Peking University Third Hospital, Beijing 100191, China.
Department of Pathology, Peking University Third Hospital, Beijing 100191, China; Department of Pathology, Peking University School of Basic Medical Sciences, Beijing 100191, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2018 Apr 18;50(2):378-380.
Here we reported a case of bronchial adenoid cystic carcinoma from Peking University Third Hospital. A 40-year-old female presented with dry cough for 1 year and nocturnal paroxysmal attacks of wheezing for 4 months. She was a non-smoker, and did not have past histories of asthma or allergy. On physical examination, no stridor, wheezing and cyanosis were present and the general appearance was good. The results of the laboratory analysis, including blood eosinophils count, immunoglobulin E level and chest X-ray were normal. Spirometry revealed reversible airflow obstruction, and post-bronchodilator forced expiratory volume in one second (FEV1) showed an increase of 12% and 230 mL from baseline. Bronchial asthma was diagnosed, however, she responded poorly despite the adequate anti-asthma therapy including high dose inhaled corticosteroid plus long-acting beta2-agonist, theophylline and montelukast. Then chest computed tomography (CT) was performed which showed a polypoid mass occupying the lumen of left main bronchus. Then the bronchoscopy revealed a polypoid endo-bronchial mass arising from the left main bronchus, causing subtotal obstruction of the lumen. Biopsy was carried out through the bronchoscopy, the pathological findings showed characteristic cribriform and tubular pattern which was formed by two-layered cells with ductal and myoepithelial phenotypes, which were consistent with adenoid cystic carcinoma. Re-examining the patient, the lung was clear without any wheeze when she was seated. However, inspiratory wheeze was heard in her left upper lung when she was supine, and disappeared after sitting up again. Subsequently the patient underwent a resection surgery. At the operational site, the tumor was seen on the anterolateral wall of the left main bronchus, without submucosally expanding histologically. Therefore, a sleeve resection surgery of the left main bronchus was performed. Following surgery, chest CT scan revealed complete resolution of the tumor. Her symptoms improved significantly, as did her pulmonary function tests, although all the medicines for asthma were stopped. Now, two years after the operation, the patient remained asymptomatic, and spirometry was performed again which showed normal completely. The presenting case report emphasizes the fact that not all wheezes and reversible airflow obstruction are asthma. It is critical to bear in mind that if a "difficult asthma" patient does not respond to appropriate anti-asthma therapy; localized obstructions should be differentiated.
在此,我们报告了北京大学第三医院的一例支气管腺样囊性癌病例。一名40岁女性,干咳1年,夜间阵发性喘息4个月。她不吸烟,既往无哮喘或过敏史。体格检查时,未闻及喘鸣、哮鸣音及发绀,一般情况良好。实验室分析结果,包括血嗜酸性粒细胞计数、免疫球蛋白E水平及胸部X线均正常。肺功能检查显示可逆性气流受限,支气管扩张剂后一秒用力呼气容积(FEV1)较基线增加12%,增加230ml。诊断为支气管哮喘,然而,尽管给予了充分的抗哮喘治疗,包括高剂量吸入糖皮质激素加长效β2受体激动剂、茶碱和孟鲁司特,她的反应仍不佳。随后进行胸部计算机断层扫描(CT),显示一个息肉样肿物占据左主支气管管腔。支气管镜检查发现一个源于左主支气管内的息肉样肿物,导致管腔部分阻塞。通过支气管镜进行活检,病理结果显示特征性的筛状和管状结构,由具有导管和肌上皮表型的两层细胞形成,符合腺样囊性癌。再次检查患者,坐位时肺部清晰,无任何哮鸣音。然而,仰卧位时左上肺可闻及吸气性哮鸣音,再次坐起后消失。随后患者接受了切除手术。在手术部位,肿瘤位于左主支气管前外侧壁,组织学上未见黏膜下扩展。因此,进行了左主支气管袖状切除术。术后胸部CT扫描显示肿瘤完全消退。她的症状明显改善,肺功能测试结果也是如此,尽管所有哮喘药物均已停用。现在,术后两年,患者仍无症状,再次进行肺功能检查显示完全正常。本病例报告强调了并非所有哮鸣音和可逆性气流受限都是哮喘这一事实。必须牢记,如果“难治性哮喘”患者对适当的抗哮喘治疗无反应,应鉴别是否存在局部阻塞。