Service d'Hépatologie, DHU Unity, Hôpital Beaujon, Assistance Publique-Hôpitaux de Paris, Clichy, France; INSERM, UMR-1149, Centre de Recherche sur l'Inflammation, Paris-Clichy, France.
Service d'Anatomie Pathologique, Hôpital Beaujon, Assistance Publique-Hôpitaux de Paris, Clichy, France; INSERM, UMR-1149, Centre de Recherche sur l'Inflammation, Paris-Clichy, France; Université Denis Diderot-Paris 7, Sorbonne Paris Cité, 75018 Paris, France.
Chest. 2019 Jan;155(1):123-136. doi: 10.1016/j.chest.2018.09.017. Epub 2018 Oct 4.
Hepatopulmonary syndrome (HPS) is characterized by an arterial oxygenation defect, defined by an increased alveolar-arterial oxygen gradient, induced by pulmonary vascular dilatations in the context of liver disease. The pathogenesis of HPS is poorly understood. Morphologic changes associated with HPS are unknown. This study aimed at describing imaging and pathology changes associated with HPS.
We performed a case-control study in candidates for transplant with suspicion of cirrhosis. Each patient with HPS (Pao ≤ 70 mm Hg) was matched to three control subjects for age, cause, and liver disease severity. Pretransplant thoracic and abdominal imaging and explanted livers were reviewed.
CT scans and Doppler ultrasounds from 21 patients with HPS were compared with those from 63 control subjects. HPS was associated with a two- to threefold higher prevalence of obstructed intrahepatic portal branches, of slowed or hepatofugal portal blood flow, and of large abdominal portosystemic shunts. Hepatic artery diameter was also larger in patients with HPS. Explanted livers from 19 patients with HPS were compared with those from 57 control subjects. HPS was associated with a fourfold higher prevalence of portal venule thrombosis and a ninefold higher prevalence of extensive vascular proliferation within fibrous septa. Obstruction of centrilobular venules, sinusoidal dilatation, and liver parenchymal extinction were also more common in patients with HPS.
HPS is associated with intrahepatic vascular changes and with features suggesting severe portal hypertension. These results raise the hypothesis that intrahepatic vascular changes precipitate the development of HPS, opening new therapeutic perspectives for HPS.
肝肺综合征(HPS)的特征是动脉血氧合缺陷,由肝脏疾病背景下的肺血管扩张引起的肺泡-动脉氧梯度增加定义。HPS 的发病机制尚未完全了解。与 HPS 相关的形态学变化尚不清楚。本研究旨在描述与 HPS 相关的影像学和病理学变化。
我们对怀疑患有肝硬化的移植候选者进行了病例对照研究。每位 HPS 患者(Pao≤70mmHg)均与 3 名年龄、病因和肝病严重程度相匹配的对照患者进行匹配。回顾性分析了患者的胸部和腹部影像学及肝移植标本。
对 21 例 HPS 患者的 CT 扫描和多普勒超声与 63 例对照患者的 CT 扫描和多普勒超声进行了比较。HPS 与肝内门静脉分支阻塞、门静脉血流减慢或肝背离、大的腹部门体分流的发生率增加两到三倍有关。HPS 患者的肝动脉直径也更大。对 19 例 HPS 患者的肝移植标本与 57 例对照患者的肝移植标本进行了比较。HPS 与门静脉小静脉血栓形成的发生率增加四倍和纤维间隔内广泛血管增生的发生率增加九倍有关。中央静脉阻塞、窦状扩张和肝实质消失在 HPS 患者中也更为常见。
HPS 与肝内血管变化和提示严重门静脉高压的特征有关。这些结果提出了肝内血管变化引发 HPS 发展的假说,为 HPS 的治疗开辟了新的前景。