Biliary atresia with splenic malformation with associated ductal plate malformation and duodenal atresia: A case report

Biliary atresia (BA) is the most common cause of the obstructive type of neonatal cholestasis that requires prompt surgical intervention. About 10% of neonates with BA have other congenital anomalies, of which splenic malformation (BASM) is a well-known distinct sub-group. There is sparse literature...

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Veröffentlicht in:Indian journal of pathology & microbiology 2024-10, Vol.67 (4), p.881-883
Hauptverfasser: Mukherjee, Raktim, Halder, Aniket, Das, Suman Kumar, Mukherjee, Suchandra, Chatterjee, Uttara
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container_issue 4
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container_title Indian journal of pathology & microbiology
container_volume 67
creator Mukherjee, Raktim
Halder, Aniket
Das, Suman Kumar
Mukherjee, Suchandra
Chatterjee, Uttara
description Biliary atresia (BA) is the most common cause of the obstructive type of neonatal cholestasis that requires prompt surgical intervention. About 10% of neonates with BA have other congenital anomalies, of which splenic malformation (BASM) is a well-known distinct sub-group. There is sparse literature on the association of duodenal atresia and ductal plate malformation (DPM) in patients of BASM. We describe a BASM associated with DPM and duodenal atresia in a 35-day-old infant, who succumbed at 40 days, before portoenterostomy could be performed. Duodenal atresia can be one of the associated malformations associated with BASM and ductal plate abnormalities. In our case, the child did not survive.
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subjects Abnormalities
Biliary atresia
Biliary Atresia - complications
Biliary Atresia - diagnosis
Biliary Atresia - surgery
Cholestasis
Congenital anomalies
Congenital defects
Duodenal Obstruction - diagnostic imaging
Duodenal Obstruction - surgery
Fatal Outcome
Female
Humans
Infant
Intestinal Atresia - surgery
Male
Neonates
Spleen
Spleen - abnormalities
Spleen - diagnostic imaging
Spleen - pathology
title Biliary atresia with splenic malformation with associated ductal plate malformation and duodenal atresia: A case report
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