Giordano Paola, Francavilla Mariantonietta, Buonamico Paolo, Suppressa Patrizia, Lastella Patrizia, Sangerardi Maria, Miniello Vito L, Scardapane Arnaldo, Lenato Gennaro M, Sabbà Carlo
1 Department of Biomedical Science and Human Oncology-Pediatric Unit, Policlinico Hospital - University of Bari Aldo Moro, Italy.
a These authors should be considered joint first authors of this work.
Vasa. 2017 May;46(3):195-202. doi: 10.1024/0301-1526/a000616. Epub 2017 Mar 1.
Liver involvement is a common manifestation of hereditary haemorrhagic telangiectasia (HHT). Although a number of studies have been carried out in adult patients, no study has ever been focused on investigating HHT-related hepatic involvement in paediatric patients. The present study aimed for the first time to systematically estimate the prevalence of HHT-associated liver involvement and to characterize HHT-associated hepatic angiodynamic features in paediatric age.
The study was designed as a cross-sectional survey in an HHT paediatric cohort, subclassified as HHT1 and HHT2 according to the mutated gene. The evaluation of the angiodynamic profile was performed by duplex ultrasound examination. Investigation by multi-slice computed tomography (MSCT) or magnetic resonance angiography (MRA) was performed in patients >12 years.
MSCT/MRA examination disclosed silent hepatic involvement in 7/20 (35.0 %) children, and nodular regenerative hyperplasia in two cases. Diameter of common hepatic artery was significantly larger in HHT2 (0.45 ± 0.15 cm) compared to HHT1 (0.33 ± 0.09, p < 0.01) and control children (0.32 ± 0.08, p < 0.05). None of the patients had clinical manifestations of liver involvement. Angiodynamic profiles were different between paediatric and adult HHT patients.
Liver involvement can be detected in paediatric HHT patients, albeit with a lower frequency compared to adults. Paediatric HHT2 children show a higher frequency of liver involvement and a trend to hepatic artery dilation when compared to HHT1 children.
肝脏受累是遗传性出血性毛细血管扩张症(HHT)的常见表现。尽管已对成年患者进行了多项研究,但从未有研究专注于调查儿科患者中与HHT相关的肝脏受累情况。本研究首次旨在系统评估HHT相关肝脏受累的患病率,并描述儿科年龄段HHT相关的肝脏血管动力学特征。
本研究设计为对HHT儿科队列进行横断面调查,根据突变基因分为HHT1和HHT2亚组。通过双功超声检查评估血管动力学特征。对12岁以上患者进行多层螺旋计算机断层扫描(MSCT)或磁共振血管造影(MRA)检查。
MSCT/MRA检查发现7/20(35.0%)例儿童存在无症状性肝脏受累,2例有结节性再生性增生。与HHT1组(0.33±0.09 cm)和对照组儿童(0.32±0.08 cm)相比,HHT2组肝总动脉直径显著更大(0.45±0.15 cm,p<0.01;p<0.05)。所有患者均无肝脏受累的临床表现。儿科和成年HHT患者的血管动力学特征不同。
儿科HHT患者可检测到肝脏受累,尽管频率低于成人。与HHT1儿童相比,儿科HHT2儿童肝脏受累频率更高,且有肝动脉扩张趋势。