右下膈动脉至右肺动脉瘘管的线圈栓塞术,同时累及其他动脉:罕见病例报告。

Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI:10.3941/jrcr.v17i8.4972
L J Juergens, A Thalhammer, T Gruber-Rouh, V Koch, T J Vogl, S S Martin
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引用次数: 0

摘要

一名 51 岁的女性患者出现呼吸困难一年多,既往未患肺部感染,也未做过手术。最初进行的计算机断层扫描诊断显示,右下膈动脉和右肺动脉之间存在罕见的动脉畸形,并在肺中叶形成血管束。由于患者呼吸困难,且畸形范围巨大,因此有了经导管动脉栓塞的指征。首次经导管动脉栓塞术涉及膈下动脉和胸内动脉的选择性分支。介入血管造影和计算机断层扫描显示,畸形进一步扩大,右侧胸腔、肝脏和下上腹动脉与瘘管相连。一个月后,对这些动脉进行了第二次经导管动脉栓塞,并对近端胸内动脉进行了第二次处理。在随访中,患者描述她的呼吸困难得到了很大改善,并且没有出现感染迹象。膈动脉肺动脉瘘是一种极为罕见的先天性或后天性疾病。患者可能没有症状,也可能出现呼吸困难、咯血、肺部感染和充血性心力衰竭等症状。有症状的患者需要使用经导管动脉栓塞或手术切除治疗。该患者呼吸困难,畸形范围较大,临床病程可能比较复杂。建议采用经导管动脉栓塞术进行微创治疗,并取得了成功。总之,我们的患者是一例罕见的全身动脉和肺动脉沟通的先天性病例,我们通过线圈栓塞术对其进行了充分治疗。
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Coil embolization of a fistula from the right inferior phrenic artery to the right pulmonary artery with involvement of further arteries: A rare case report.

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.

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