Long term survival of a biliary atresia patient by repeated liver transplantations for portopulmonary hypertension in addition to the hepatopulmonary syndrome
A female patient after Kasai procedure for biliary atresia had a hepatopulmonary syndrome(HPS), and underwent living donor liver transplantation (LDLT)at 15 years old. HPS improved once, but unfortunately recurred with the graft dysfunction 10 years later, and portopulmonary hypertension (PoPH) addi...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Elsevier,
2023-02-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |