Reichert Martin, Kerber Stefanie, Alkoudmani Ibrahim, Bodner Johannes
Department of General, Visceral, Thoracic, Transplant and Pediatric Surgery, University Hospital of Giessen, Rudolf-Buchheim Street 7, 35392, Giessen, Germany.
Department of Visceral, Transplant and Thoracic Surgery, Innsbruck Medical University, Anichstrasse 35, 6020, Innsbruck, Austria.
Surg Endosc. 2016 Apr;30(4):1667-9. doi: 10.1007/s00464-015-4337-0. Epub 2015 Jul 9.
Pulmonary arteriovenous malformations are abnormal communications between the pulmonary arterial and venous vasculature leading to a right-to-left blood shunt. Based on possible complications, including hypoxemia, hemorrhage, infection and paradoxical embolism, deactivation of the malformation from the circulation is the treatment option of choice, either by interventional embolization or by surgery. Embolization is less invasive and has widely replaced surgery, but bears the risk of revascularization, recanalization and downstream migration of the device with paradoxical embolism.
We report on the case of a 76-year-old male patient suffering from a complex, plexiform pulmonary arteriovenous malformation in the lingula, which was treated by video-assisted thoracoscopic surgery and anatomic lingula resection. Patient's medical history, clinical examination and imaging studies did not reveal any evidence of hereditary hemorrhagic telangiectasia.
Left-sided anterior three-port video-assisted thoracoscopic surgery (VATS) approach was used. Instead of only wedge resecting the very peripherally located pulmonary arteriovenous malformation, the lingular vessels were controlled centrally and an anatomic lingula resection was performed in order to prevent a more central re-malformation. To prevent rupture of the aneurysm sac through pressure overload, the feeding arteries were controlled before the draining vein. Duration of the total procedure was 151 min, the single chest tube was removed on the postoperative day 3, and the patient was discharged on the postoperative day 6.
Although interventional embolism of the feeding artery of a pulmonary arteriovenous malformation is the current therapeutic gold standard, minimally invasive anatomic lung resection by video-assisted thoracoscopic surgery can be considered, especially for the treatment of solitary large arteriovenous malformations. By anatomic lung resection, the risk of recanalization, collateralization and peri-interventional paradoxical embolism may be reduced.
肺动静脉畸形是肺动脉和静脉系统之间的异常交通,导致右向左分流。基于可能出现的并发症,包括低氧血症、出血、感染和反常栓塞,使畸形从循环中失活是首选的治疗方法,可通过介入栓塞或手术实现。栓塞的侵入性较小,已广泛取代手术,但存在血管再通、再灌注以及装置下游迁移并伴有反常栓塞的风险。
我们报告了一例76岁男性患者,其舌叶患有复杂的丛状肺动静脉畸形,通过电视辅助胸腔镜手术和解剖性舌叶切除术进行治疗。患者的病史、临床检查和影像学检查均未发现遗传性出血性毛细血管扩张的任何证据。
采用左侧前入路三端口电视辅助胸腔镜手术(VATS)方法。并非仅楔形切除位于非常周边的肺动静脉畸形,而是在中心部位控制舌叶血管,并进行解剖性舌叶切除术,以防止更中心部位再次形成畸形。为防止动脉瘤囊因压力过载而破裂,在引流静脉之前先控制供血动脉。整个手术持续时间为151分钟,术后第3天拔除单根胸管,患者于术后第6天出院。
尽管肺动静脉畸形供血动脉的介入栓塞是当前的治疗金标准,但对于孤立性大动静脉畸形的治疗,尤其是通过电视辅助胸腔镜手术进行微创解剖性肺切除也可予以考虑。通过解剖性肺切除,可降低再通、侧支形成和介入期间反常栓塞的风险。