Univ Lille, CHU Lille, Department of Thoracic Imaging, Cardio-Pulmonary Institute, Boulevard Jules Leclercq, F-59000, Lille, France.
Department of Biostatistics, University Center of Lille, F-59000, Lille, France.
Eur Radiol. 2022 Jul;32(7):4574-4586. doi: 10.1007/s00330-022-08577-x. Epub 2022 Mar 14.
In the stratification of potential causes of PH, current guidelines recommend performing V/Q lung scintigraphy to screen for CTEPH. The recognition of CTEPH is based on the identification of lung segments or sub-segments without perfusion but preserved ventilation. The presence of mismatched perfusion defects has also been described in a small proportion of idiopathic pulmonary arterial hypertension (PAH) and pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis (PVOD/PCH). Dual-energy CT lung perfusion changes have not been specifically investigated in these two entities.
To compare dual-energy CT (DECT) perfusion characteristics in PAH and PVOD/PCH, with specific interest in PE-type perfusion defects.
Sixty-three patients with idiopathic or heritable PAH (group A; n = 51) and PVOD/PCH (group B; n = 12) were investigated with DECT angiography with reconstruction of morphologic and perfusion images.
The number of patients with abnormal perfusion did not differ between group A (35/51; 68.6%) and group B (6/12; 50%) (p = 0.31) nor did the mean number of segments with abnormal perfusion per patient (group A: 17.9 ± 4.9; group B: 18.3 ± 4.1; p = 0.91). The most frequent finding was the presence of patchy defects in group A (15/35; 42.9%) and a variable association of perfusion abnormalities in group B (4/6; 66.7%). The median percentage of segments with PE-type defects per patient was significantly higher in group B than in group A (p = 0.041). Two types of PE-type defects were depicted in 8 patients (group A: 5/51; 9.8%; group B: 3/12; 25%), superimposed on PH-related lung abnormalities (7/8) or normal lung (1/8). The iodine concentration was significantly lower in patients with abnormal perfusion (p < 0.001) but did not differ between groups.
Perfusion abnormalities did not differ between the two groups at the exception of a higher median percentage of segments with PE-type defects in patients with PVOD/PCH.
• Patchy perfusion defect was the most frequent pattern in PAH. • A variable association of perfusion abnormalities was seen in PVOD/PCH. • Lobular and PE-type perfusion defects larger than a sub-segment were depicted in both PAH and PVOD/PCH patients.
在肺动脉高压(PH)潜在病因的分层中,目前的指南建议进行 V/Q 肺闪烁显像以筛查 CTEPH。CTEPH 的识别基于无灌注但保留通气的肺段或亚段的识别。在一小部分特发性肺动脉高压(PAH)和肺静脉闭塞性疾病和/或肺毛细血管血管瘤病(PVOD/PCH)中,也描述了不匹配的灌注缺陷。双能 CT 肺灌注变化尚未在这两种实体中专门研究过。
比较 PAH 和 PVOD/PCH 中双能 CT(DECT)灌注特征,特别关注 PE 型灌注缺陷。
对 63 例特发性或遗传性 PAH 患者(A 组,n = 51)和 PVOD/PCH 患者(B 组,n = 12)进行 DECT 血管造影检查,对形态和灌注图像进行重建。
A 组(35/51;68.6%)和 B 组(6/12;50%)患者的异常灌注发生率无差异(p = 0.31),每个患者异常灌注的平均段数也无差异(A 组:17.9 ± 4.9;B 组:18.3 ± 4.1;p = 0.91)。最常见的发现是 A 组(15/35;42.9%)存在斑片状缺陷,B 组(4/6;66.7%)存在不同程度的灌注异常。B 组患者中 PE 型缺陷的中位数每例段数明显高于 A 组(p = 0.041)。8 例患者(A 组:5/51;9.8%;B 组:3/12;25%)显示 2 种类型的 PE 型缺陷,分别叠加在 PH 相关肺异常(7/8)或正常肺(1/8)上。异常灌注患者的碘浓度明显降低(p < 0.001),但两组之间没有差异。
两组之间的灌注异常没有差异,但 PVOD/PCH 患者中 PE 型缺陷的中位数比例较高。
• PAH 最常见的灌注缺损模式为斑片状。
• PVOD/PCH 患者的灌注异常存在不同程度的关联。
• 在 PAH 和 PVOD/PCH 患者中,均可见小叶和 PE 型灌注缺损大于亚段。