General Medicine, Medway Maritime Hospital, Gillingham, UK
General Medicine, Medway Maritime Hospital, Gillingham, UK.
BMJ Case Rep. 2021 Sep 20;14(9):e244712. doi: 10.1136/bcr-2021-244712.
Hepatopulmonary syndrome (HPS) is a serious complication of chronic liver disease, characterised by portal hypertension and arterial hypoxaemia due to intrapulmonary vascular dilatation. We report an unusual case in which a 27-year-old man had a first presentation of portal hypertension and cirrhosis complicated by HPS. This patient presented with progressive dyspnoea on exertion and deterioration in mobility, with a type 1 respiratory failure and increased oxygen demand. A bubble echocardiogram showed a possible right-to-left shunt, CT aortogram displayed evidence of portal hypertension and cirrhosis, and liver biopsy findings were consistent with alpha-1 antitrypsin deficiency. The patient's increased oxygen demand was subsequently treated with continuous positive airway pressure before he was discharged with 8 L home oxygen. With no current established medical therapy for HPS, the patient was assessed for liver transplantation and a decision was made in favour of this.
肝肺综合征(HPS)是慢性肝病的严重并发症,其特征为门静脉高压和由于肺内血管扩张导致的动脉低氧血症。我们报告了一例不常见的病例,一名 27 岁男性首次出现门静脉高压和肝硬化合并 HPS。该患者表现为进行性运动性呼吸困难和活动能力恶化,伴有 1 型呼吸衰竭和增加的氧气需求。超声心动图显示可能存在右向左分流,主动脉 CT 造影显示门静脉高压和肝硬化的证据,肝活检结果符合α-1 抗胰蛋白酶缺乏症。患者的高氧需求随后通过持续气道正压通气治疗,然后在出院时使用 8 L 家庭氧气。由于目前尚无针对 HPS 的既定医学治疗方法,对患者进行了肝移植评估,并决定进行肝移植。