Department of Pathology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
Hospital Eduardo Schütz Schroeder, Puerto Montt, Chile.
Br J Haematol. 2019 Apr;185(2):317-326. doi: 10.1111/bjh.15795. Epub 2019 Feb 10.
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.
肺部并发症在镰状细胞病(SCD)患者中很常见,但很少有研究描述过 SCD 的肺部病理学。我们研究了 30 名已故 SCD 患者(1994-2012 年)的肺组织。介绍了人口统计学、基因型、临床特征、死亡原因和相关情况。我们量化了肺动脉变化、血栓形成和静脉增厚的存在。使用 CD34 表达和共聚焦显微镜显示了肺泡毛细血管异常。回顾尸检和超声心动图报告以对心脏异常进行分类。在肺血管中定量了内皮细胞激活标志物(血管细胞黏附分子 1、细胞间黏附分子 1 和血管内皮生长因子)的组织表达。中位年龄为 33 岁;19 例为 SS 基因型,7 例为 SC 基因型,4 例为 Sβ 基因型,18 例为男性。76%的患者存在高血压性动脉改变,80%的患者存在近期血栓形成,43%的患者存在陈旧性血栓形成。23%的患者存在静脉增厚,87%的患者存在肺毛细血管血管瘤灶。10%的患者存在右心室肥厚。与对照组相比,内皮激活标志物的表达没有增加。SCD 影响整个肺血管树,反映了疾病随时间对肺血管造成的多重负担。