Menon Jagadeesh, Vij Mukul, Shanmugam Naresh, Hakeem Abdul, Reddy Mettu Srinivas, Kaliamoorthy Ilankumaran, Rela Mohamed
Department of Pediatric Gastroenterology & Hepatology, Dr. Rela Institute & Medical Centre, Chennai, Tamil Nadu, India.
Department of Histopathology, Dr. Rela Institute & Medical Centre, Chennai, Tamil Nadu, India.
J Pediatr Genet. 2020 Sep 28;11(2):165-170. doi: 10.1055/s-0040-1716829. eCollection 2022 Jun.
Fibropolycystic diseases of the liver comprise a spectrum of disorders affecting bile ducts of various sizes and arise due to an underlying ductal plate malformation (DPM). We encountered a previously unreported variant of DPM, the hilar fibropolycystic disease which we diagnosed in the explant liver. A 2-year-old boy was referred for liver transplantation with a diagnosis of biliary atresia (BA) and failed Kasai portoenterostomy (KPE). He had cirrhosis with portal hypertension along with synthetic failure indicated by coagulopathy and hypoalbuminemia. The child underwent liver transplant successfully. The explant liver had fibropolycystic disease confined to the perihilar liver and hilum. No pathogenic mutation was detected by whole exome sequencing. Fibropolycystic liver disease may represent a peculiar anatomical variant, which can be diagnosed by careful pathological examination of the explant liver. The neonatal presentation of hilar fibropolycystic liver disease can be misdiagnosed as BA.
肝脏纤维多囊性疾病包括一系列影响不同大小胆管的病症,其起因是潜在的胆管板畸形(DPM)。我们遇到了一种先前未报道的DPM变体,即肝门部纤维多囊性疾病,我们在移植肝中诊断出了这种疾病。一名2岁男孩因诊断为胆道闭锁(BA)且Kasai肝门空肠吻合术(KPE)失败而被转诊进行肝移植。他患有肝硬化伴门静脉高压,同时存在凝血障碍和低白蛋白血症所提示的肝功能衰竭。该患儿成功接受了肝移植。移植肝的纤维多囊性疾病局限于肝门周围肝脏和肝门。全外显子测序未检测到致病突变。纤维多囊性肝病可能代表一种特殊的解剖学变体,可通过对移植肝进行仔细的病理检查来诊断。肝门部纤维多囊性肝病的新生儿表现可能被误诊为BA。