Goethe University Frankfurt, University Hospital, Department of Diagnostic and Interventional Radiology, Germany.
J Radiol Case Rep. 2023 Aug 1;17(9):22-28. doi: 10.3941/jrcr.v17i8.4972. eCollection 2023 Sep.
A 51-year-old female patient was presenting dyspnea for more than a year with no previous lung infections or surgery. Initially, a diagnostic computed tomography was made, showing a rare arterio-arterial malformation between the right inferior phrenic and right pulmonary artery leading into a vascular bundle in the middle lung lobe. Due to the patients' dyspnea and massive extent of malformation, the indication for transcatheter arterial embolization was made. The first transcatheter arterial embolization procedure involved the inferior phrenic and a selective branch of the internal thoracic artery. Interventional angiography as well as computed tomography revealed further extend of the malformation showing a connection of right lateral thoracic, hepatic, and inferior epigastric artery to the fistula. After one month, a second transcatheter arterial embolization of these arteries as well as a second approach of the proximal internal thoracic artery was performed. In the follow-up the patient described a substantial improvement of her dyspnea and showed no signs of infections. A phrenic artery to pulmonary artery fistula is an extremely rare case occurring congenital or acquired. Patients may be asymptomatic or present, among others, dyspnea, hemoptysis, pulmonary infections and congestive heart failure. Symptomatic patients require treatment using transcatheter arterial embolization or surgical resection. The patient had dyspnea and a substantial extent of malformation with possibly complicated clinical course. The recommended less invasive treatment using transcatheter arterial embolization was successfully performed. In conclusion, our patient represented a rare congenital case of systemic and pulmonary artery communication, which we were able to treat sufficiently with coil embolization.
一位 51 岁女性患者因呼吸困难超过一年就诊,无既往肺部感染或手术史。最初进行了诊断性 CT 检查,显示右下膈神经和右肺动脉之间存在罕见的动脉-动脉畸形,导致中叶血管束进入。由于患者呼吸困难和畸形范围广泛,因此进行了经导管动脉栓塞治疗。第一次经导管动脉栓塞治疗涉及膈神经和胸内动脉的选择性分支。介入血管造影和 CT 显示畸形进一步扩展,显示右侧胸外侧、肝和下腹部动脉与瘘管相连。一个月后,对这些动脉以及胸内动脉近端进行了第二次经导管动脉栓塞治疗。在随访中,患者描述呼吸困难明显改善,且无感染迹象。肺动静脉瘘是一种非常罕见的先天性或后天性疾病。患者可能无症状,也可能表现为呼吸困难、咯血、肺部感染和充血性心力衰竭等症状。有症状的患者需要采用经导管动脉栓塞或手术切除治疗。该患者存在呼吸困难和广泛的畸形,且可能存在复杂的临床病程。推荐采用经导管动脉栓塞的微创治疗方法,并成功完成。总之,我们的患者代表了一种罕见的先天性体循环和肺循环沟通,我们通过线圈栓塞成功地对其进行了充分治疗。