Congenital extrahepatic portosystemic shunts (CEPS) are rare anomalies connecting the portal system to the inferior vena cava. This report discusses a 10-year-old boy with Type II c CEPS, presenting cyanosis and dyspnea. Surgical ligation resulted in significant improvement in symptoms. Early identification and intervention are crucial, necessitating a protocolized approach.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11324084 | PMC |
| http://dx.doi.org/10.4103/jiaps.jiaps_1_24 | DOI Listing |
Publication Analysis
Top Keywords
congenital extrahepatic
8
extrahepatic portosystemic
8
surgically correctable
4
correctable central
4
central cyanosis
4
cyanosis congenital
4
portosystemic shunt
4
shunt child
4
child congenital
4
portosystemic shunts
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!