Chronic Thromboembolic Pulmonary Hypertension (CTEPH) Post-Pulmonary Endarterectomy
Imaging findings
Pre-operative CT demonstrates signs of severe pulmonary hypertension, including right ventricular hypertrophy and dilation, septal flattening, and a massive pulmonary artery. Marked mosaic attenuation is present in the lung parenchyma due to distal arterial occlusions. Post-pulmonary endarterectomy CT shows a dramatic decrease in the size of the right ventricle, and the mosaic perfusion is nearly completely resolved, reflecting the restoration of homogenous distal blood flow.
Key takeaways
CTEPH is characterized by chronic fibrotic thrombi obstructing pulmonary arterial branches, leading to severe pulmonary hypertension and mosaic lung perfusion. Pulmonary endarterectomy is the treatment of choice, and successful surgical clearance of the vessels can be visualized post-operatively on CT by the normalization of right heart size and the dramatic resolution of mosaic perfusion patterns.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Lupus-Associated Interstitial Lung Disease (Fibrotic NSIP with Cystic Changes)ILD
- Lobar TorsionIatrogenic
- Mixed Dust Pneumoconiosis (Desert Sand Exposure)Exposure
- Recurrent Lymphangioleiomyomatosis (LAM) Post-Lung TransplantILD
- Geliophysic DysplasiaCongenital
- Anomalous Left Coronary Artery from the Opposite Sinus (ACAOS) with Intramural CourseCongenital
- Pulmonary Amyloidosis (Cystic and Calcified)Metabolic
- Endobronchial Metastases from Colon AdenocarcinomaNeoplastic
See all cases from August 28, 2021 →
Related Vascular cases
- Post-Thromboendarterectomy Pulmonary Hemorrhage
- Spontaneous Coronary Artery Dissection (SCAD)
- Post-Lobectomy Pulmonary Vein Stump Thrombus
- Pulmonary Thromboembolism Mimicking Pulmonary Artery Sarcoma
- Plexiform Arteriopathy in Idiopathic Pulmonary Arterial Hypertension
- CTEPH with Pulmonary Artery-to-Pulmonary Artery Collaterals