Goldsmith Ira, George Joseph, Aslam Umair, Sharma Sobaran
Department of Cardiothoracic Surgery, Swansea Bay University Health Board, Morriston Hospital, Swansea, Wales, SA6 6NL, UK.
J Cardiothorac Surg. 2021 Apr 13;16(1):78. doi: 10.1186/s13019-021-01470-6.
Congenital pulmonary airway malformation (CPAM) with partial anomalous pulmonary venous connection presenting as episodic retrosternal chest pain on exertion in an adult has not been described.
A 21-year-old female, non-smoker, presented with a 4-year history of sharp, episodic, retrosternal chest pains brought on with exercise. A contrast-enhanced computed tomography (CT) scan showed a grossly overinflated left lower lobe with partial anomalous pulmonary venous drainage into the left hemi-azygos vein. Lobectomy, the recommended treatment of choice, carried out thoracoscopically, was curative with satisfactory mid-term results. Histology confirmed type-II congenital pulmonary airway malformation.
CPAM can present in young adults with unusual symptoms of chest pain on exertion. When suspected a contrast-enhanced CT scan is the gold standard for establishing the diagnosis. An anatomical lung resection is curative with satisfactory medium term results.
成人先天性肺气道畸形(CPAM)合并部分性肺静脉异位连接表现为运动时发作性胸骨后胸痛的情况尚未见报道。
一名21岁不吸烟女性,有4年运动时发作性尖锐胸骨后胸痛病史。增强计算机断层扫描(CT)显示左下叶明显过度充气,部分肺静脉异常引流至左半奇静脉。推荐的治疗选择是胸腔镜下肺叶切除术,该手术具有治愈性且中期效果良好。组织学证实为II型先天性肺气道畸形。
CPAM可在年轻成人中表现为运动时胸痛的不寻常症状。怀疑时,增强CT扫描是确诊的金标准。解剖性肺切除术具有治愈性且中期效果良好。