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Preduodenal portal vein: a case series of variable clinical presentations and surgical implications
Ahmed Arafa1, Abdelhafeez Mohamed Abdelhafez2, Ahmed S Ragab3
1Pediatric Surgery Department, Faculty of Medicine, Cairo University, Cairo, Egypt. drahmedarafa1@gmail.com.
Insights
Four pediatric cases of preduodenal portal vein (PDPV) showed varied presentations, from incidental findings to causing duodenal obstruction. Recognizing PDPV during surgery is vital for appropriate management and avoiding complications.
Area of Science:
- Pediatric Surgery
- Gastrointestinal Surgery
- Vascular Anomalies
Background:
- Preduodenal portal vein (PDPV) is a rare congenital anomaly.
- PDPV can be asymptomatic or cause significant gastrointestinal issues.
- Association with other congenital anomalies, such as extrahepatic biliary atresia (EHBA), is noted.
Purpose of the Study:
- To report a case series of pediatric patients with PDPV.
- To illustrate the diverse clinical presentations and surgical management strategies for PDPV.
- To emphasize the importance of intraoperative recognition of PDPV.
Main Methods:
- Retrospective review of four pediatric cases with PDPV.
- Analysis of clinical presentations, intraoperative findings, and surgical interventions.
- Correlation of PDPV with associated anomalies and obstructive symptoms.
Main Results:
- Two cases of PDPV were incidentally found during surgery for EHBA and required no specific intervention.
- Two cases presented with duodenal obstruction; one due to PDPV compression, managed with laparoscopic duodenoduodenostomy.
- One case of duodenal obstruction was due to malrotation, with PDPV noted but not causative; treated with Ladd's procedure.
Conclusions:
- PDPV exhibits variable clinical manifestations, from incidental intraoperative findings to significant duodenal obstruction.
- Accurate intraoperative identification of PDPV is critical for surgical planning and patient safety.
- Management should be tailored based on whether PDPV is the obstructing factor or an incidental finding, especially in the presence of other anomalies.
Aim Of The Study:
To present a case series of four pediatric patients with PDPV, each with a different clinical presentation and surgical management.
Methods:
We retrospectively reviewed four cases of PDPV managed at our institution. Two cases were associated with extrahepatic biliary atresia (EHBA) and discovered incidentally during surgery. The other two cases presented with duodenal obstruction but had differing etiologies and management approaches.
Results:
Two patients with EHBA underwent successful Kasai portoenterostomy; PDPV was discovered intraoperatively and required no intervention. One patient had duodenal obstruction due to PDPV compressing the duodenum and underwent laparoscopic duodenoduodenostomy. Another patient had duodenal obstruction due to malrotation; a Ladd's procedure was performed. PDPV was noted intraoperatively but was not the obstructing factor.
Conclusion:
PDPV can present variably, ranging from an incidental finding to a causative factor in duodenal obstruction. Its recognition is crucial during abdominal surgery to avoid inadvertent injury and to tailor the surgical approach based on associated anomalies.
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