ArticleThe Journal of international medical research2025
Congenital extrahepatic portosystemic shunts (Abernethy malformation): A report of two cases.
Article in The Journal of international medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.