Han Ji-Won, Kim Hyun-Young, Jung Sung-Eun
Department of Surgery, Seoul National University Children's Hospital, Seoul, Korea.
Medicine (Baltimore). 2017 Feb;96(6):e5240. doi: 10.1097/MD.0000000000005240.
Few case reports of umbilical arteriovenous malformation (AVM) have been reported. Herein, we report a neonatal case of umbilical AVM who underwent liver failure after surgical excision.
The patient was a girl delivered at a gestational age of 39+5 weeks showing cyanosis and heart murmur.
Cardiac echography, abdominal ultrasonography (USG), and computed tomography revealed suspecting the umbilical AVM.
On the eighth day after birth, because of the aggravation of heart failure, emergency surgery for excision of umbilical AVM was performed.
In postoperative state, worsened laboratory test of liver function and coagulopathy indicated the liver failure. Abdominal USG revealed that the portal vein (PV) flow primarily occurred from the left PV to the inferior vena cava via ductus venosus and coarse hepatic echogenicity. After conservative management, laboratory findings of liver function and the flow direction of the left PV were normal, as demonstrated by abdominal USG within 50th postoperative day.
Careful preoperative evaluation of an AVM of a large size with significant blood flow should be performed, and the possibility of liver failure after surgery should always be considered.
脐动静脉畸形(AVM)的病例报告很少。在此,我们报告一例新生儿脐AVM,其在手术切除后发生肝功能衰竭。
该患者为一名孕39 + 5周出生的女孩,表现为发绀和心脏杂音。
心脏超声、腹部超声(USG)和计算机断层扫描显示怀疑为脐AVM。
出生后第8天,由于心力衰竭加重,进行了紧急手术切除脐AVM。
术后状态下,肝功能实验室检查恶化和凝血功能障碍提示肝功能衰竭。腹部USG显示门静脉(PV)血流主要通过静脉导管从左PV流向肝下腔静脉,肝脏回声粗糙。经过保守治疗,术后第50天腹部USG显示肝功能实验室检查结果和左PV血流方向正常。
对于大尺寸且血流显著的AVM,应进行仔细的术前评估,并始终考虑术后发生肝功能衰竭的可能性。