Pulmonary endarterectomy for chronic thromboembolic pulmonary hypertension after bilateral lung transplantation

Bianca Battilana MD , Jan Mengers MD , György Lang MD , Martina Haberecker MD , Claudio Caviezel MD , Macé M. Schuurmans MD , Silvia Ulrich MD , Isabelle Opitz MD FEBTS, Prof. Dr. med.
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Abstract

Case report

A 30-year-old woman suffering from diffuse interstitial lung disease underwent bilateral lung transplantation in 2008. A high-risk bilateral pulmonary embolism (PE) occurred in 2020 after deep venous thrombosis. After lysis (Endovascular System and oral anticoagulation), 1-year follow-up imaging showed a persisting thrombus-load (Fig. 1). Right heart catheterization (RHC) 18 months after PE showed s/m/dPAP of 51/34/25mmHg, PVR of 5.6WU and CO 4.43l/min. Echocardiography demonstrated right ventricular dilation with impaired radial and longitudinal function. She reported worsening dyspnea (NYHA III) and impaired lung function (FEV1 1.3 l, DLCO 43%, best post-transplant value: FEV1 2.44 l, DLCO 68%) without diagnosis of CLAD. CT-imaging showed organized thrombotic material in the right inferior lobe and left pulmonary artery (Fig. 1). In 2022, bilateral PEA under deep hypothermic circulatory arrest was performed. On the right, multiple segments were obliterated, whereas in the left main trunk a cone-shaped occlusion of the complete left main PA at the level of the anastomosis was resected in addition to peripheral lesions (Fig. 1 and 2). Histopathological evaluation revealed cartilaginous metaplasia of the tunica intima (Fig. 2). This phenomenon represents a vascular remodeling process in which chronic thromboembolic injury, inflammation, TGF-β1-mediated vascular smooth muscle cell transdifferentiation, and transplant-related stress collectively drive the formation of cartilage-like tissue, resulting in irreversible maladaptive remodeling and pulmonary hypertension.
The patient was extubated on the first postoperative day and discharged to rehabilitation after 14 days. After 7 weeks, she reported improved performance (NYHA I), and echocardiography showed decreased sPAP (from 45 to 37 mmHg). 18-month postoperatively the patient was in an excellent condition, reported further improvements in performance (NYHA I) and RHC showing s/m/dPAP of 30/19/11mmHg, PVR 4.1WU and CO 3.65l/min.
肺内膜切除术治疗双侧肺移植后慢性血栓栓塞性肺动脉高压
病例报告:一位患有弥漫性间质性肺病的30岁女性于2008年接受了双侧肺移植。2020年发生了一例深静脉血栓形成后的高危双侧肺栓塞(PE)。溶解后(血管内系统和口服抗凝),1年随访成像显示持续存在血栓负荷(图1)。术后18个月右心导管造影显示s/m/dPAP为51/34/25mmHg, PVR为5.6WU, CO为4.43l/min。超声心动图显示右心室扩张,径向和纵向功能受损。她报告呼吸困难加重(NYHA III)和肺功能受损(FEV1 1.3 l, DLCO 43%,最佳移植后值:FEV1 2.44 l, DLCO 68%),但未诊断为CLAD。ct成像显示右下叶和左肺动脉有组织血栓物质(图1)。2022年,在深度低温循环停搏下进行了双侧PEA。在右侧,多个节段被切除,而在左侧主干,除了切除周围病变外,还切除了吻合处完整左侧主干PA的锥形闭塞(图1和2)。组织病理学检查显示内膜软骨化生(图2)。这一现象代表了慢性血栓栓塞损伤、炎症、TGF-β1介导的血管平滑肌细胞转分化和移植相关应激共同驱动软骨样组织形成的血管重构过程,导致不可逆的不适应重构和肺动脉高压。患者术后第一天拔管,14天后出院康复。7周后,患者报告表现改善(NYHA I),超声心动图显示sPAP下降(从45降至37 mmHg)。术后18个月,患者病情良好,表现进一步改善(NYHA I), RHC显示s/m/dPAP为30/19/11mmHg, PVR为4.1WU, CO为3.65l/min。
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