From the Department of Pediatrics, Gazi University, Ankara, Turkey.
Exp Clin Transplant. 2024 Oct;22(Suppl 5):117-123. doi: 10.6002/ect.pedsymp2024.P6.
Extrahepatic portal vein obstruction is the most common cause of portal hypertension in children. This study aimed to evaluate the causes, clinical, laboratory and endoscopic findings, treatment approaches, long-term results, and prognosis of extrahepatic portal vein obstruction in children.
We retrospectively evaluated 82 patients who were followed up with the diagnosis of extrahepatic portal vein obstruction at Gazi University Pediatric Gastroenterology clinic between January 1, 2011, and October 31, 2021.
Among our patients, 58.5% were male, median age at presentation was 36 months (range, 1 month to 6 years), and the follow-up period was 2 years (range, 1-14 years). The most common reasons for admission were gastrointestinal bleeding and splenomegaly. All patients diagnosed with incidentally detected obstruction were children under 5 years of age. The most frequently detected risk factors were history of umbilical vein catheterization (50%) and presence of procoagulant status (31%). Esophageal varices (94.8%), variceal bleeding (73.2%), hypersplenism (64.6%), and growth failure (13.4%) were the most common complications. Weight and/or height z-scores were lower in children with esophageal varices, variceal bleeding, and hypersplenism. Endoscopic treatments were more frequently applied to those with splenomegaly, thrombocytopenia, red color sign, and esophageal variceal bleeding. Rates of splenomegaly, hypersplenism, esophageal variceal bleeding, advanced varicose veins, and portal biliopathy were higher in patients who underwent portosystemic shunt surgery than in patients who did not undergo it.
Morbidity and mortality rates of variceal bleeding in extrahepatic portal vein obstruction were lower than bleeding seen in cirrhotic prehepatic portal hypertension. In our study, no patients died from extrahepatic portal vein obstruction-related complications. One patient died from tuberculous meningitis.
肝外门静脉阻塞是儿童门静脉高压症最常见的原因。本研究旨在评估儿童肝外门静脉阻塞的病因、临床、实验室和内镜表现、治疗方法、长期结果和预后。
我们回顾性评估了 2011 年 1 月 1 日至 2021 年 10 月 31 日期间在加济大学儿科胃肠病学诊所接受肝外门静脉阻塞诊断的 82 名患者。
在我们的患者中,58.5%为男性,中位发病年龄为 36 个月(范围为 1 个月至 6 岁),随访期为 2 年(范围为 1-14 年)。最常见的入院原因是胃肠道出血和脾肿大。所有意外发现阻塞的患者均为 5 岁以下儿童。最常见的危险因素是脐静脉导管史(50%)和存在促凝状态(31%)。食管静脉曲张(94.8%)、静脉曲张出血(73.2%)、脾功能亢进(64.6%)和生长发育迟缓(13.4%)是最常见的并发症。有食管静脉曲张、静脉曲张出血和脾功能亢进的儿童体重和/或身高 z 评分较低。内镜治疗更多地应用于脾肿大、血小板减少、红色征和食管静脉曲张出血的患者。行门体分流术的患者脾肿大、脾功能亢进、食管静脉曲张出血、静脉曲张进展和门脉性胆病的发生率高于未行门体分流术的患者。
肝外门静脉阻塞的静脉曲张出血的发病率和死亡率低于肝前门静脉高压症的出血。在我们的研究中,没有患者因肝外门静脉阻塞相关并发症而死亡。一名患者死于结核性脑膜炎。