Department of Pediatric Surgery, Hôpitaux Universitaires Paris-Sud (AP-HP), Hôpital Bicêtre, 78, avenue du Général Leclerc, 94270, Le Kremlin-Bicêtre, France.
Department of Pediatric Radiology, Hôpitaux Universitaires Paris-Sud (AP-HP), Hôpital Bicêtre, 78, avenue du Général Leclerc, 94270, Le Kremlin-Bicêtre, France.
J Pediatr Surg. 2020 Sep;55(9):1885-1891. doi: 10.1016/j.jpedsurg.2020.01.009. Epub 2020 Jan 29.
Focal nodular hyperplasia (FNH) is a rare benign hepatic lesion in children. No management guidelines for pediatric population exist because of limited evidence.
To review the experience of a large tertiary liver center, providing additional clinical data to help formulate management guidelines for FNH in the pediatric population.
We analyzed data of children <18 years diagnosed with FNH from 1996 to 2018 at our hospital, detailing management and long-term clinical outcome.
50 patients were identified. The median age was 10 years old (range 0.75-15.5 years old). The mean diameter of FNH was 5.9 cm (±3.1 cm). 10 patients had multiple lesions. First-line management: watchful waiting with serial checks (n = 37), surgery (n = 13). Of the watchful waiting patients, 10 required eventual second-line surgery. After a median follow-up of 4.7 years (range 0.5-20 years), 46 patients were asymptomatic, with no significant difference in clinical outcome (p = 0.962) between the two first-line management approaches. Lesions demonstrated growth in 13 cases: 5 of these required second-line surgery. In these patients, there was no significant difference in clinical outcome (p = 0.188) compared to nonoperative patients. Considering all surgically treated patients, there was no significant difference between first-line and second-line surgery for clinical outcome (p = 0.846), hospital stay (p = 0.410), complications (p = 0.510) and severe complications (p = 0.385).
Our data support the hypothesis that watchful waiting is a safe initial approach to pediatric FNH management in patients with no major symptoms or complications. Surgery should be reserved for patients with diagnostic doubt, persistent symptoms and/or biological or significant anatomical abnormalities. FNH growth alone should not be considered as an indication for surgery.
Therapeutic study.
Level III.
局灶性结节性增生(FNH)是儿童期罕见的良性肝病变。由于证据有限,尚无针对儿科人群的管理指南。
回顾一家大型三级肝脏中心的经验,提供更多的临床数据,帮助制定儿科人群 FNH 的管理指南。
我们分析了我院 1996 年至 2018 年间诊断为 FNH 的<18 岁儿童的数据,详细描述了管理和长期临床结果。
共确定了 50 例患者。中位年龄为 10 岁(范围为 0.75-15.5 岁)。FNH 的平均直径为 5.9cm(±3.1cm)。10 例患者有多发性病变。一线管理:观察等待与定期检查(n=37),手术(n=13)。在观察等待的患者中,有 10 例最终需要二线手术。中位随访时间为 4.7 年(范围 0.5-20 年),46 例患者无症状,两种一线管理方法的临床结果无显著差异(p=0.962)。13 例病变有生长:其中 5 例需要二线手术。在这些患者中,与非手术患者相比,临床结果无显著差异(p=0.188)。考虑所有手术治疗的患者,一线和二线手术的临床结果(p=0.846)、住院时间(p=0.410)、并发症(p=0.510)和严重并发症(p=0.385)无显著差异。
我们的数据支持这样的假设,即对于无主要症状或并发症的儿科 FNH 患者,观察等待是一种安全的初始管理方法。对于诊断存疑、持续存在症状和/或存在生物学或明显解剖异常的患者,应保留手术治疗。单纯 FNH 生长不应作为手术指征。
治疗性研究。
III 级。