Successful management of concomitant omphalocele, accessory hepatic lobe, and biliary atresia in a 44-day-old boy.

Abstract:

:We report the second case in literature of a boy with the association of large omphalocele, accessory hepatic lobe, and biliary atresia, and the first successful treatment. The patient was submitted to a surgical treatment at 44 days of life, including Kasai procedure, correction of the remnant abdominal wall defect, and removal of a hepatic accessory lobe. The boy evolved with normalization of hepatic function tests. After 15 years of follow-up, the patient is completely healthy, weights 45 kg, and is 1.64 m tall.

journal_name

J Pediatr Surg

authors

Pereira RM,Simões e Silva AC,Leite VH,Lanna JC,Guimarães JT

doi

10.1016/j.jpedsurg.2005.06.034

subject

Has Abstract

pub_date

2005-10-01 00:00:00

pages

e21-4

issue

10

eissn

0022-3468

issn

1531-5037

pii

S0022-3468(05)00500-2

journal_volume

40

pub_type

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