{"title":"先天性肝外门系统分流(畸形):附2例报告。","authors":"Yiqi Ma, Zhiming Cui, Jibo Hu","doi":"10.1177/03000605251388884","DOIUrl":null,"url":null,"abstract":"<p><p>Abernethy malformation, also known as congenital extrahepatic portosystemic shunt, is an extremely rare vascular anomaly that alters systemic hemodynamics and may lead to progressive liver dysfunction, portal hypertension, and, in advanced stages, malignant transformation or hepatic encephalopathy. The condition is frequently associated with other congenital anomalies, most notably cardiac malformations such as septal defects, patent foramen ovale, Tetralogy of Fallot, and valvular regurgitation as well as skeletal abnormalities. We report the cases of two patients-one with type Ib and the other with type II Abernethy malformation. Both patients were asymptomatic, with the diagnosis established through contrast-enhanced computed tomography and magnetic resonance imaging. Clinical, laboratory, and imaging data were collected. Given the absence of overt clinical manifestations, both patients are being managed with semiannual follow-up. Abernethy malformation is difficult to diagnose based on clinical presentation alone; however, characteristic imaging features can facilitate a definitive diagnosis. Recognition of this rare entity and its potential comorbidities is essential for timely diagnosis and appropriate management.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"53 10","pages":"3000605251388884"},"PeriodicalIF":1.5000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Congenital extrahepatic portosystemic shunts (Abernethy malformation): A report of two cases.\",\"authors\":\"Yiqi Ma, Zhiming Cui, Jibo Hu\",\"doi\":\"10.1177/03000605251388884\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Abernethy malformation, also known as congenital extrahepatic portosystemic shunt, is an extremely rare vascular anomaly that alters systemic hemodynamics and may lead to progressive liver dysfunction, portal hypertension, and, in advanced stages, malignant transformation or hepatic encephalopathy. The condition is frequently associated with other congenital anomalies, most notably cardiac malformations such as septal defects, patent foramen ovale, Tetralogy of Fallot, and valvular regurgitation as well as skeletal abnormalities. We report the cases of two patients-one with type Ib and the other with type II Abernethy malformation. Both patients were asymptomatic, with the diagnosis established through contrast-enhanced computed tomography and magnetic resonance imaging. Clinical, laboratory, and imaging data were collected. Given the absence of overt clinical manifestations, both patients are being managed with semiannual follow-up. Abernethy malformation is difficult to diagnose based on clinical presentation alone; however, characteristic imaging features can facilitate a definitive diagnosis. Recognition of this rare entity and its potential comorbidities is essential for timely diagnosis and appropriate management.</p>\",\"PeriodicalId\":16129,\"journal\":{\"name\":\"Journal of International Medical Research\",\"volume\":\"53 10\",\"pages\":\"3000605251388884\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of International Medical Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/03000605251388884\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/10/23 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of International Medical Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/03000605251388884","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/23 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
Congenital extrahepatic portosystemic shunts (Abernethy malformation): A report of two cases.
Abernethy malformation, also known as congenital extrahepatic portosystemic shunt, is an extremely rare vascular anomaly that alters systemic hemodynamics and may lead to progressive liver dysfunction, portal hypertension, and, in advanced stages, malignant transformation or hepatic encephalopathy. The condition is frequently associated with other congenital anomalies, most notably cardiac malformations such as septal defects, patent foramen ovale, Tetralogy of Fallot, and valvular regurgitation as well as skeletal abnormalities. We report the cases of two patients-one with type Ib and the other with type II Abernethy malformation. Both patients were asymptomatic, with the diagnosis established through contrast-enhanced computed tomography and magnetic resonance imaging. Clinical, laboratory, and imaging data were collected. Given the absence of overt clinical manifestations, both patients are being managed with semiannual follow-up. Abernethy malformation is difficult to diagnose based on clinical presentation alone; however, characteristic imaging features can facilitate a definitive diagnosis. Recognition of this rare entity and its potential comorbidities is essential for timely diagnosis and appropriate management.
期刊介绍:
_Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis.
As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible.
Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence.
Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements.
Print ISSN: 0300-0605