首页> 外文期刊>Journal of Medical Case Reports >Hybrid video-assisted thoracoscopic surgery lobectomy of fissureless congenital cystic adenomatoid malformation: a case report
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Hybrid video-assisted thoracoscopic surgery lobectomy of fissureless congenital cystic adenomatoid malformation: a case report

机译:混合视频辅助胸腔镜手术肺叶切除术治疗无裂隙先天性囊性腺瘤样畸形一例

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Introduction Thoracoscopic lobectomy for congenital pulmonary airway malformation has been indicated from the neonatal period to adolescence. However, it is difficult to approach the pulmonary artery for lobectomy in congenital lung malformations with incomplete or absent interlobar fissures. Multidetector computed tomographic images and computed tomography pulmonary angiography gave us helpful information before the operation. We performed thoracoscopic lobectomy for congenital pulmonary airway malformations with absent interlobar fissures and adhesions in accordance with information from multidetector computed tomographic images. Case presentation A 14-year-old Japanese girl received a diagnosis of congenital pulmonary airway malformation when she presented with pneumonia. Using multidetector computed tomography and three-dimensional reconstruction provides meticulous characterization of the anatomy in pediatric patients. We confirmed that her left A4+5 artery arose from her left pulmonary artery medial to A6. Her left pulmonary artery was divided just proximal to the A6 origin before the lobes were separated safely. We took advantage of using a stapler to divide the fissureless thick parenchyma. Perioperative diagnosis was congenital cystic adenomatoid malformation. Conclusions We used preoperative multidetector computed tomography to outline the bronchovascular anatomy and guide hybrid video-assisted thoracoscopic surgery for a congenital cystic adenomatoid malformation in a fissureless left lung.
机译:引言从新生儿期到青春期,已建议使用胸腔镜肺叶切除术治疗先天性肺气道畸形。但是,对于先天性肺畸形,叶间裂不完整或不存在的肺叶切除术,很难接近肺动脉。多探测器计算机断层扫描图像和计算机断层扫描肺血管造影在手术前为我们提供了有用的信息。我们根据多探测器计算机断层扫描图像的信息,对先天性肺气道畸形进行了胸腔镜肺叶切除术,没有叶间裂和粘连。病例介绍一名14岁的日本女孩出现肺炎时被诊断为先天性肺气道畸形。使用多探测器计算机断层扫描和三维重建技术可细致地表征小儿患者的解剖结构。我们确认她的左A4 + 5动脉从左肺动脉内侧升至A6。在安全分开肺叶之前,将她的左肺动脉在A6起源的近端分开。我们利用订书机来划分无裂隙的薄壁实质。围手术期诊断为先天性囊性腺瘤样畸形。结论我们使用术前多探测器计算机断层扫描来概述支气管血管的解剖结构,并指导混合视频辅助胸腔镜手术治疗先天性无裂隙性左肺囊性腺瘤样畸形。

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