Szmygin Maciej, Pyra Krzysztof, Sojka Michał, Jargiełło Tomasz
Department of Interventional Radiology and Neuroradiology, Medical University of Lublin, Poland.
Pol J Radiol. 2021 Feb 15;86:e112-e114. doi: 10.5114/pjr.2021.103975. eCollection 2021.
Pulmonary sequestration is a rare congenital malformation characterised by the presence of non-functional and dysplastic pulmonary tissue that lacks communication with the tracheobronchial tree and has an aberrant non-pulmonary blood supply. Depending on its location, presence of the pleura covering, and venous drainage, 2 forms of pulmonary sequestration have been described: intra- and extralobar. Traditionally, surgical resection was performed; however, a growing number of cases have been treated with endovascular intervention.
A 38-year-old female patient was admitted to the hospital with severe haemoptysis for several hours. Examination at admission revealed tachycardia and tachypnoea. Computed tomography-examination disclosed the presence of an area of consolidation in the left lower lobe with a tortuous feeding artery arising from the descending aorta. Visible ground glass opacification indicated diffuse alveolar haemorrhage. Based on these findings, a diagnosis of intralobar sequestration of the left lung was made. The patient was consulted by a cardiothoracic surgeon and an interventional radiologist and qualified for endovascular treatment. In local anaesthesia femoral access was obtained and selective angiography of the common trunk of both bronchial arteries was performed. It depicted a dilated left bronchial artery supplying the sequestration and visible contrast extravasation. Embolisation of the vessel was performed with Glubran (n-butyl-cyanoacrylate). Control contrast injection showed complete elimination of the sequestration's blood supply with no residual capillary blush. Clinical improvement was observed. No complications were encountered, and the patient was discharged 7 days after the procedure.
Arterial embolisation is a promising alternative to surgery in the treatment of symptomatic pulmonary sequestration.
肺隔离症是一种罕见的先天性畸形,其特征是存在无功能且发育异常的肺组织,该组织与气管支气管树不相通,且有异常的非肺血供。根据其位置、是否有胸膜覆盖以及静脉引流情况,肺隔离症可分为两种类型:叶内型和叶外型。传统上采用手术切除;然而,越来越多的病例采用血管内介入治疗。
一名38岁女性患者因严重咯血数小时入院。入院检查发现心动过速和呼吸急促。计算机断层扫描检查显示左下叶有一个实变区域,有一条迂曲的供血动脉发自降主动脉。可见磨玻璃样混浊提示弥漫性肺泡出血。基于这些发现,诊断为左肺叶内型隔离症。心胸外科医生和介入放射科医生对该患者进行了会诊,认为其适合进行血管内治疗。在局部麻醉下经股动脉穿刺,对双侧支气管动脉的共同主干进行了选择性血管造影。造影显示左支气管动脉增粗,为隔离症供血,可见造影剂外渗。用Glubran(正丁基氰基丙烯酸酯)对该血管进行了栓塞。对照造影剂注射显示隔离症的血供完全消除,无残留毛细血管造影剂外溢。临床症状有所改善。未出现并发症,患者在术后7天出院。
动脉栓塞是治疗有症状肺隔离症的一种有前景的替代手术的方法。