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Updated: May 19, 2026

Isolation of Neonatal Extrahepatic Cholangiocytes
Published on: June 5, 2014
[Neonatal intrahepatic cholestasis caused by citrin deficiency: a histopathologic study of 10 cases]
Guang-yu Jiang1, Zhao-ming Cheng, Kai-shan Liu
1Department of Pathology, the First Affiliated Hospital of Jinan University, Guangzhou, China.
Objective:
To investigate the diagnostic value of histopathological changes in the liver of patients with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).
Methods:
Liver specimens from 10 cases of NICCD were evaluated by hematoxylin-eosin stain, histochemistry and immunohistochemistry (EnVision method). SLC25A13 mutation analysis was performed to correlate with histopathology.
Results:
Most specimens showed varying degrees of fat deposition in hepatocytes, necrotic inflammation, cholestasis and fibrosis (so-called tetralogy). The combination of the above four histological changes was highly characteristic for NICCD. With the progression of the disease, hepatic fibrosis deteriorated and ultimately led to cirrhosis.
Conclusions:
NICCD should be suspected in the presence of cholestasis during infancy. A liver biopsy must be performed to rule out other liver diseases. The tetralogy of the hepatic histopathological changes has a highly diagnostic value for NICCD, which is also practical for accurately assessing the degree of inflammation and fibrosis, and similarly the progression of hepatic cirrhosis.
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