Mehta Asmita Anilkumar, Viswanathan Naveen, Vasudevan Anil Kumar, Paulose Roopa, Abraham Mohan
Clinical Professor, Department of Pulmonary Medicine, Amrita Institute of Medical Sciences , Ponekara, Kochi, Kerala, India .
Clinical Professor, Department of Paediatric Surgery, Amrita Institute of Medical Sciences , Ponekara, Kochi, Kerala, India .
J Clin Diagn Res. 2016 Nov;10(11):SC01-SC04. doi: 10.7860/JCDR/2016/19205.8775. Epub 2016 Nov 1.
Congenital Cystic Adenomatoid Malformation (CCAM) is an uncommon developmental deformity affecting the terminal respiratory structures. It is characterized by broncho pulmonary foregut malformations. The reason behind it is an arrest in lung development between 4 and 7 week of fetal life.
The present study was conducted to assess the clinical and radiological profile and also to study the role of surgical intervention in patients with CCAM.
All patients with clinical suspicion or provisional diagnosis of CCAM were included in the study. A clinical questionnaire was prepared to collect data. Computed Tomography (CT) chest with High Resolution Computed Tomography (HRCT) was done for all the patients. Patients were assessed by paediatric surgeon and eligible patients were operated. The procedure conducted was usually open thoracotomy under general anaesthesia. The affected lobes were removed and specimens were sent for histopathological analysis. All included patients were followed up prospectively to find out about their current level of health. Via telephonic interview they were asked about their overall growth, quality of life, activity, rate of respiratory infections and requirement of hospital admission.
Total 15 patients with diagnosis of CCAM were included in the study. Of them, 8 (53.3%) were male. The commonest presentation was cough 13(86%), breathing difficulty 11(73%), fever 9(60%), recurrent pneumonia 4(26%), hypoxia requiring oxygen supplementation 6(40%), others 2(12%). Thirteen patients required surgical intervention and underwent lobectomy. There were 2 cases of type I, one each of type II and III, 3 case of type IV while 5 were intermediate type. There was no procedure related mortality. The median duration of hospital stay and all were successfully discharged with median duration of stay 11±16 days.
The study concludes that if recognized early, surgical removal of affected lung prevents the complications like recurrent pulmonary infections. The surgery is well tolerated without any post-operative mortality or morbidity.
先天性囊性腺瘤样畸形(CCAM)是一种影响终末呼吸结构的罕见发育畸形。其特征为支气管肺前肠畸形。其病因是胎儿期4至7周时肺发育停滞。
本研究旨在评估CCAM患者的临床和放射学特征,并研究手术干预在其中的作用。
所有临床怀疑或初步诊断为CCAM的患者均纳入本研究。编制了一份临床问卷以收集数据。对所有患者进行了胸部计算机断层扫描(CT)及高分辨率计算机断层扫描(HRCT)。由小儿外科医生对患者进行评估,符合条件的患者接受手术。所实施的手术通常是在全身麻醉下进行开胸手术。切除受影响的肺叶,并将标本送去做组织病理学分析。对所有纳入研究的患者进行前瞻性随访,以了解他们目前的健康状况。通过电话访谈询问他们的整体生长情况、生活质量、活动情况、呼吸道感染发生率及住院需求。
本研究共纳入15例诊断为CCAM的患者。其中,8例(53.3%)为男性。最常见的表现为咳嗽13例(86%)、呼吸困难11例(73%)、发热9例(60%)、反复肺炎4例(26%)、需要吸氧的低氧血症6例(40%)、其他2例(12%)。13例患者需要手术干预并接受了肺叶切除术。其中I型2例,II型和III型各1例,IV型3例,5例为中间型。无手术相关死亡。中位住院时间为11±16天,所有患者均成功出院。
本研究得出结论,若早期诊断,手术切除患肺可预防反复肺部感染等并发症。手术耐受性良好,无术后死亡或发病情况。