Biliary atresia is a rare disease characterized by a biliary obstruction of unknown origin that presents in the neonatal period.1 We present the magnetic resonance cholangiography (MRC) from a 25 years old women who was treated in the neonatal period with Kasai operation. The MRC reveals a choledochal cyst and shows multiple saccular dilatation of both left and right hepatic ducts.
Journal Information
Vol. 7. Issue 4.
Pages 381 (October - December 2008)
Vol. 7. Issue 4.
Pages 381 (October - December 2008)
Open Access
A 25 years old women after Kasai operation for biliary atresia
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References
[1.]
Chardot C..
Biliary atresia.
Orphanet J Rare Dis, 1 (2006), pp. 28
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