Brief Article
Copyright ©2012 Baishideng Publishing Group Co.
World J Gastroenterol. Nov 21, 2012; 18(43): 6255-6262
Published online Nov 21, 2012. doi: 10.3748/wjg.v18.i43.6255
Table 1 Patients with liver disease and patients who underwent liver transplantation
DiseaseDiagnosisn (M/F)
Liver diseaseAlcoholic liver cirrhosis152 (94/58)
Autoimmune hepatitis type I77 (27/50)
Viral hepatitis B117 (67/50)
Viral hepatitis C147 (82/65)
Wilson’s disease31 (13/18)
Primary biliary cirrhosis32 (4/28)
Primary sclerosing cholangitis59 (40/19)
Nonalcoholic steatohepatitis23 (10/12)
Liver steatosis132 (77/55)
Budd-Chiari syndrome14 (5/9)
Polycystic liver10 (1/9)
Others1168 (74/94)
OLTxAlcoholic liver cirrhosis164 (131/33)
Autoimmune hepatitis type I33 (11/22)
Viral hepatitis B33 (20/13)
Viral hepatitis C79 (56/23)
Wilson’s disease29 (12/17)
Primary biliary cirrhosis40 (5/35)
Primary sclerosing cholangitis64 (47/17)
Cryptogenic liver cirrhosis28 (16/12)
Budd-Chiari syndrome6 (2/4)
Polycystic liver14 (3/11)
Others233 (16/17)
Table 2 Immunoglobulin A anti-tissue transglutaminase seropositivity in patients with liver disease and patients who underwent liver transplantation
IgA anti-tTG seropositivityDiagnosisM/Fn (%)
Liver diseaseWilson’s disease1/34 (12.9)
Autoimmune hepatitis type I1/45 (6.5)
Primary biliary cirrhosis0/11 (3.1)
Budd-Chiari syndrome0/11 (7.1)
Mild hepatic liver tests abnormalities5/27 (20)
Liver steatosis3/14 (3.3)
Viral hepatitis B1/01 (0.9)
Toxic hepatitis1/01 (4.8)
Nonalcoholic steatohepatitis0/22 (8.7)
Primary sclerosing cholangitis1/12 (3.4)
Polycystic liver0/11 (10)
OLTxWilson’s disease1/12 (6.9)
Autoimmune hepatitis type I0/22 (6.1)
Alcoholic liver cirrhosis1/01 (0.6)
Table 3 Patients with liver disease newly diagnosed with celiac disease
No.AgeGenderDiagnosisLiver histology
134FPSCPortal tracts with ductular reaction and minimal inflammation, features of chronic cholestasis
237MPSCFlorid ductular reaction with accompanying mild mixed inflammation and focal dark-brown granules of copper-associated protein (in orcein stain) in periportal hepatocytes
333MWilson's d.Macrovesicular steatosis, periportal fibrosis and periportal hepatocytes with glycogenated nuclei
435FWilson's d.Focal steatosis, periportal and septal fibrosis
536FWilson's d.Mild nonspecific hepatocellular injury with spotty hepatocyte necrosis and mononuclear portal
inflammatory infiltrate, scattered apoptotic bodies and mild steatosis
629MAIH type IPortal and lobular inflammation, periportal fibrosis
733FAIH type IPortal and periportal inflammation, spotty necrosis
833FAIH type IChronic hepatitis pattern of injury with portal-based inflammation and fibrosis
940FAIH type IPeriportal interface activity and scattered hepatocyte necrosis
1035FPBCBile duct injury with epithelioid granuloma, portal inflammation
1132MToxic hepatitisPortal inflammation with scattered eosinophils, spotty necrosis
1250FBudd-Chiari s.Extensive centrilobular necrosis of hepatocytes
1322MCeliac hepatitisNon-specific reactive hepatitis with mild portal inflammation
1427MCeliac hepatitisMild lobular inflammation with apoptotic bodies and hepatocyte necrosis
1550FCeliac hepatitisMild periportal fibrosis with mild portal inflammation and focal interface activity
1640FNASHBallooned hepatocytes, macrovesicular steatosis accentuated in zone 3 without significant liver injury