- Author:
Guang-yu JIANG
1
;
Zhao-ming CHENG
;
Kai-shan LIU
Author Information
- Publication Type:Journal Article
- MeSH: Biopsy; Calcium-Binding Proteins; deficiency; genetics; metabolism; Cholestasis, Intrahepatic; etiology; genetics; pathology; Disease Progression; Female; Hepatocytes; pathology; Humans; Infant; Liver; pathology; Liver Cirrhosis; pathology; Male; Mitochondrial Membrane Transport Proteins; genetics; Mutation; Organic Anion Transporters; deficiency; genetics; metabolism
- From: Chinese Journal of Pathology 2012;41(7):452-455
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the diagnostic value of histopathological changes in the liver of patients with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).
METHODSLiver 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.
RESULTSMost 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.
CONCLUSIONSNICCD 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.