Neonatal Cholestasis

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Variations in Biliary Atresia
Clinical Features History: Variable degrees of persistent jaundice, dark urine, light colored stools, +/-poor appetite * Usually Well-Appearing* Physical: Hepatomegaly, +/- splenomegaly “appear” well-nourised Usually with decreased fat stores and lean body mass Enlarged abdomen from HSM may give impression of “normal weight for age” Scleral icterus, abdominal wall veins (caput medusa) Labs: Total bilirubin rarely is >12mg/dL; CB is usually
Page 1 and 2: Neonatal Cholestasis Jenny Bergquis
Page 3 and 4: Neonatal Cholestasis NASPGHAN Recom
Page 5 and 6: Differential Diagnosis: Hepatocellu
Page 7 and 8: Physical Exam Weight measurement
Page 9 and 10: NASPGHAN Recommendations: Imaging S
Page 11: Biliary Atresia: pathogenesis Bile
Page 15 and 16: “Triangular Cord” Sign
Page 17: Surgical Management Kasai Procedur
Page 20 and 21: If Kasai Fails? +/- support for re
Page 22 and 23: What happened to our patient? Kasa

Neonatal Cholestasis

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