Clinical relevance of pulmonary vasculature involvement in sickle cell disease. (10th February 2019)

• Record Type: Journal Article
• Authors: Carstens, German R.; Paulino, Bianca B. A.; Katayama, Edgard H.; Amato‐Lourenço, Luis F.; Fonseca, Guilherme H.; Souza, Rogerio; Aiello, Vera D.; Mauad, Thais
• Is Part Of: British journal of haematology. Volume 185:Number 2(2019)
• Page Start: 317
• Page End: 326
• Publication Date: 2019-02-10
• Subjects: sickle cell -- lung -- pathology -- pulmonary capillary haemangiomatosis -- thrombosis; Hematology -- Periodicals; Blood -- Diseases -- Periodicals; 616.15
• DOI: 10.1111/bjh.15795
• Languages: English
• ISSNs: 0007-1048

Abstract

Summary: Pulmonary complications are frequent in patients with sickle cell disease (SCD), but few studies have described lung pathology in SCD. We studied the lung tissue of 30 deceased SCD patients (1994–2012). Demographics, genotype, clinical characteristics, cause of death and associated conditions are presented. We quantified the presence of pulmonary arterial changes, thrombosis and venous thickening. Alveolar capillary abnormalities were demonstrated using CD34 expression and confocal microscopy. Autopsy and echocardiography reports were reviewed to classify heart abnormalities. Tissue expression of markers of endothelial activation (vascular cell adhesion molecule 1, intercellular adhesion molecule 1 and vascular endothelial growth factor) was quantified in pulmonary vessels. Median age was 33 years; genotype was SS in 19, SC in 7 and Sβ in 4, and there were 18 males. Hypertensive arterial changes were present in 76% of the patients, recent thrombosis in 80% and old thrombosis in 43%. Venous thickening was present in 23% and pulmonary capillary haemangiomatosis foci in 87%. Ten percent of the patients presented right ventricular hypertrophy. There was no increased expression of endothelial activation markers when compared to controls. SCD affects the whole pulmonary vascular tree and reflects the multiple burden on lung vasculature imposed by the disease upon time.