BA: Biliary Atresia With Rare Associations, a Case Report

Sponsor
Sarah Magdy Abdelmohsen (Other)
Overall Status
Completed
CT.gov ID
NCT05917236
Collaborator
(none)
1
1
12
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Study Details

Study Description

Brief Summary

Background: It is not often written in medical journals that preduodenal portal vein, biliary atresia, intestinal malrotation, and situs inversus totalis are all related.

Case reports: A two-month-old female infant had biliary atresia type III, situs inversus totalis, midgut malrotation, and preduodenal portal vein. She had been operated on by the Kasai procedure (hepato-portoenterostomy).

Discussion: It is important to carefully look into the relationship between preduodenal portal vein and biliary atresia because the patient at a risk of injury from this aberrant vein at operative intervention.

Condition or Disease Intervention/Treatment Phase
  • Procedure: hepato-portoentostomy

Detailed Description

A full-term female infant, G1P1, weighing 3450 g at birth, was referred to our department at the age of 2 months old with severe jaundice and poor feeding. The mother reported yellow sclera and skin, lightning-colored stool, and dark colored urine a few days after birth, which were progressively aggravated.

On physical examination, the infant had an olive-green colored sclera and skin with an itching mark, a pale clay stool in the diaper, a law grade fever of 37.8°C, a weight of 3870 g, a pulse rate of 138 b/m, and a respiratory rate of 38 b/m. The heart sounds and breath sounds were normal. The abdomen was soft and lax on examination. The liver was two fingers below the costal margin. The intestinal sound was normal.

The laboratory investigation revealed that total bilirubin was elevated at 7 mg/dl, direct bilirubin was elevated at 4 mg/dl, GGT was elevated at 157,1 U/L, alkaline phosphatase was elevated at 279 U/L, and albumin was decreased at 3.4 g/dL.

Abdominal ultrasonography revealed a triangular cord sign in the liver hilum, an absent gall bladder, and a normal-sized spleen on the right side behind the liver. A chest x-ray revealed dextrocardia. The HIDA scan revealed failure of radioisotope excretion in the duodenum . Non-contrast magnetic resonance cholangiopancreatography (MRCP) showed that the common hepatic duct and the common bile duct could not be seen. Preoperative percutaneous liver biopsy reported liver fibrosis, bile ductules proliferation and cholestasis.

An experienced pediatric surgeon obtained the decision for exploratory laparotomy by right subcostal abdominal incision. The spleen is located in the right upper quadrant behind the liver. Extracorporealization of the liver is done . The gall bladder was rudimentary. On further exploration, the principle investigator also found intestinal malrotation (IM) and PDPV. All extrahepatic bile ducts were absent; type III portal atresia. The portal palate was dissected easily and the rudimentary gall bladder was removed.

Widening of the narrow base of the intestinal mesentery, then reconstruction of the retro-colic Roux-en-Y limb of the jejunum, and finally hepato-portoentostomy (Kasai operation) was done . A wedge liver biopsy obtained reported ductular proliferation, hepatic fibrosis, and bile plugs; a feature suggestive of biliary obstruction.

The post-operative follow-up of the patient revealed features of bile drainage in the intestine; the stool returned to its normal brawn color; and the yellow skin color was slightly improved. Total bilirubin was 4 mg/dl and direct bilirubin was 2 mg/dl. The patient was discharged on the tenth post-operative day.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
1 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Biliary Atresia and Preduodenal Portal Vein
Actual Study Start Date :
Sep 1, 2021
Actual Primary Completion Date :
Sep 1, 2021
Actual Study Completion Date :
Sep 1, 2022

Outcome Measures

Primary Outcome Measures

  1. Is the infant will still a live or he will dies? [from 3 weeks to one year follow up]

    Is the infant will continue his life up to one year or he will dies during the follow-up period.

Eligibility Criteria

Criteria

Ages Eligible for Study:
2 Months to 3 Months
Sexes Eligible for Study:
Female
Inclusion Criteria:
  • Biliary atresia with another syndrome
Exclusion Criteria:
  • Biliary atresia alone

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aswan university Aswan Sahary Egypt 81528

Sponsors and Collaborators

  • Sarah Magdy Abdelmohsen

Investigators

  • Study Director: Sarah M Abdelmohsen, Lecturer, Aswan University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sarah Magdy Abdelmohsen, Principal Investigator, Aswan University Hospital
ClinicalTrials.gov Identifier:
NCT05917236
Other Study ID Numbers:
  • AswanUH4
First Posted:
Jun 23, 2023
Last Update Posted:
Jun 23, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 23, 2023