Vascular Ehlers–Danlos syndrome (vEDS): CT and histologic findings of pleural and lung parenchymal damage

• Published in: European radiology 2021-08, Vol.31 (8), p.6275-6285
• Main Authors: Boussouar, Samia, Benattia, Amira, Escudié, Jean.-Baptiste, Gibault, Laure, Capron, Frédérique, Legrand, Anne, Brillet, Pierre-Yves, Jeunemaitre, Xavier, Grenier, Philippe A., Mousseaux, Elie, Frank, Michael, Sanchez, Olivier
• Format: Article
• Language: English
• Subjects: Abnormalities; Alveoli; Asymptomatic; Chest; Computed tomography; Diagnostic Radiology; Diagnostic systems; Ehlers-Danlos syndrome; Emphysema; Hemoptysis; Hemorrhage; Hemothorax; Imaging; Internal Medicine; Interventional Radiology; Lung nodules; Lungs; Medical imaging; Medicine; Medicine & Public Health; Mutation; Neuroradiology; Nodules; Patients; Physicians; Pneumothorax; Point mutation; Radiology; Respiration; Smoking; Statistical analysis; Statistical methods; Surgery; Thoracic surgery; Thorax; Ultrasound
• ISSN: 0938-7994; 1432-1084
• DOI: 10.1007/s00330-021-07710-6

Objectives To describe CT features of lung involvement in patients with vascular Ehlers–Danlos syndrome (vEDS), a rare genetic condition caused by pathogenic variants within the COL3A1 gene, characterized by recurrent arterial, digestive, and pulmonary events. Material and methods All consecutive vEDS patients referred to the national tertiary referral center for vEDS, between 2004 and 2016, were included. Chest CT scans obtained during the initial vascular work-up were reviewed retrospectively by two chest radiologists for lung involvement. Five surgical samples underwent histologic examination. Results Among 136 enrolled patients (83 women, 53 men; mean age 37 years) with molecularly confirmed vEDS, 24 (17.6%) had a history of respiratory events: 17 with pneumothorax, 4 with hemothorax, and 3 with hemoptysis that required thoracic surgery in 11. CT scans detected lung parenchymal abnormalities in 78 (57.3%) patients: emphysema (mostly centrilobular and paraseptal) in 44 (32.3%), comparable for smokers and non-smokers; clusters of calcified small pulmonary nodules in 9 (6.6%); and cavitated nodules in 4 (2.9%). Histologic examination of surgical samples found arterial abnormalities, emphysema with alveolar ruptures in 3, accompanied by diffuse hemorrhage and increased hemosiderin resorption. Conclusion In vEDS patients, identification of lung parenchymal abnormalities is common on CT. The most frequently observed CT finding was emphysema suggesting alveolar wall rupture which might facilitate the diagnostic screening of the disease in asymptomatic carriers of a genetic COL3A1 gene mutation. The prognostic value and evolution of these parenchymal abnormalities remain to be evaluated. Key Points • Patients with vEDS can have lung parenchymal changes on top of or next to thoracal vascular abnormalities and that these changes can be present in asymptomatic cases. • The presence of these parenchymal changes is associated with a slightly higher incidence of respiratory events (although not statistically significant). • Identification of the described CT pattern by radiologists and chest physicians may facilitate diagnostic screening.