Jagadisan Barath, Dhawan Anil
Pediatric Liver GI and Nutrition Centre and MowatLabs, King's College Hospital, London, UK.
Pediatric Liver GI and Nutrition Centre and MowatLabs, King's College Hospital, London, UK.
J Hepatol. 2022 May;76(5):1199-1214. doi: 10.1016/j.jhep.2021.12.027. Epub 2022 Jan 3.
The aetiology of several liver diseases in children is age specific and many of these conditions have significant and potentially long-term clinical repercussions if not diagnosed early and managed in a timely fashion. We address 5 clinical scenarios that cover most of the diagnostic and therapeutic emergencies in children: infants with liver disease; acute liver failure; management of bleeding varices; liver-based metabolic disorders; and liver tumours and trauma. A wide spectrum of conditions that cause liver disease in infants may present as conjugated jaundice, which could be the only symptom of time-sensitive disorders - such as biliary atresia, metabolic disorders, infections, and haematological/alloimmune disorders - wherein algorithmic multistage testing is required for accurate diagnosis. In infantile cholestasis, algorithmic multistage tests are necessary for an accurate early diagnosis, while vitamin K, specific milk formulae and disease-specific medications are essential to avoid mortality and long-term morbidity. Management of paediatric acute liver failure requires co-ordination with a liver transplant centre, safe transport and detailed age-specific aetiological work-up - clinical stabilisation with appropriate supportive care is central to survival if transplantation is indicated. Gastrointestinal bleeding may present as the initial manifestation or during follow-up in patients with portal vein thrombosis or chronic liver disease and can be managed pharmacologically, or with endoscopic/radiological interventions. Liver-based inborn errors of metabolism may present as encephalopathy that needs to be recognised and treated early to avoid further neurological sequelae and death. Liver tumours and liver trauma are both rare occurrences in children and are best managed by a multidisciplinary team in a specialist centre.
儿童多种肝脏疾病的病因具有年龄特异性,如果不及早诊断并及时处理,其中许多病症会产生重大且可能长期的临床影响。我们讨论了5种临床情况,涵盖了儿童大多数诊断和治疗急症:患有肝脏疾病的婴儿;急性肝衰竭;静脉曲张出血的处理;基于肝脏的代谢紊乱;以及肝脏肿瘤和创伤。多种导致婴儿肝脏疾病的病症可能表现为结合胆红素血症,这可能是一些时间敏感型疾病(如胆道闭锁、代谢紊乱、感染以及血液系统/同种免疫疾病)的唯一症状,对于这些疾病,需要进行多阶段的系统性检查以准确诊断。在婴儿胆汁淤积症中,多阶段的系统性检查对于准确的早期诊断是必要的,而维生素K、特定的婴儿配方奶粉和针对疾病的药物对于避免死亡和长期发病至关重要。小儿急性肝衰竭的处理需要与肝移植中心协调、安全转运以及针对不同年龄的详细病因检查——如果需要进行移植,通过适当的支持治疗实现临床稳定是生存的关键。胃肠道出血可能是门静脉血栓形成或慢性肝病患者的初始表现或在随访期间出现,可以通过药物治疗,或内镜/放射学干预进行处理。基于肝脏的先天性代谢缺陷可能表现为脑病,需要尽早识别并治疗以避免进一步的神经后遗症和死亡。肝脏肿瘤和肝脏创伤在儿童中都很少见,最好由专科中心的多学科团队进行处理。