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©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
Published online Nov 21, 2012. doi: 10.3748/wjg.v18.i43.6255
Disease | Diagnosis | n (M/F) |
Liver disease | Alcoholic liver cirrhosis | 152 (94/58) |
Autoimmune hepatitis type I | 77 (27/50) | |
Viral hepatitis B | 117 (67/50) | |
Viral hepatitis C | 147 (82/65) | |
Wilson’s disease | 31 (13/18) | |
Primary biliary cirrhosis | 32 (4/28) | |
Primary sclerosing cholangitis | 59 (40/19) | |
Nonalcoholic steatohepatitis | 23 (10/12) | |
Liver steatosis | 132 (77/55) | |
Budd-Chiari syndrome | 14 (5/9) | |
Polycystic liver | 10 (1/9) | |
Others1 | 168 (74/94) | |
OLTx | Alcoholic liver cirrhosis | 164 (131/33) |
Autoimmune hepatitis type I | 33 (11/22) | |
Viral hepatitis B | 33 (20/13) | |
Viral hepatitis C | 79 (56/23) | |
Wilson’s disease | 29 (12/17) | |
Primary biliary cirrhosis | 40 (5/35) | |
Primary sclerosing cholangitis | 64 (47/17) | |
Cryptogenic liver cirrhosis | 28 (16/12) | |
Budd-Chiari syndrome | 6 (2/4) | |
Polycystic liver | 14 (3/11) | |
Others2 | 33 (16/17) |
IgA anti-tTG seropositivity | Diagnosis | M/F | n (%) |
Liver disease | Wilson’s disease | 1/3 | 4 (12.9) |
Autoimmune hepatitis type I | 1/4 | 5 (6.5) | |
Primary biliary cirrhosis | 0/1 | 1 (3.1) | |
Budd-Chiari syndrome | 0/1 | 1 (7.1) | |
Mild hepatic liver tests abnormalities | 5/2 | 7 (20) | |
Liver steatosis | 3/1 | 4 (3.3) | |
Viral hepatitis B | 1/0 | 1 (0.9) | |
Toxic hepatitis | 1/0 | 1 (4.8) | |
Nonalcoholic steatohepatitis | 0/2 | 2 (8.7) | |
Primary sclerosing cholangitis | 1/1 | 2 (3.4) | |
Polycystic liver | 0/1 | 1 (10) | |
OLTx | Wilson’s disease | 1/1 | 2 (6.9) |
Autoimmune hepatitis type I | 0/2 | 2 (6.1) | |
Alcoholic liver cirrhosis | 1/0 | 1 (0.6) |
No. | Age | Gender | Diagnosis | Liver histology |
1 | 34 | F | PSC | Portal tracts with ductular reaction and minimal inflammation, features of chronic cholestasis |
2 | 37 | M | PSC | Florid ductular reaction with accompanying mild mixed inflammation and focal dark-brown granules of copper-associated protein (in orcein stain) in periportal hepatocytes |
3 | 33 | M | Wilson's d. | Macrovesicular steatosis, periportal fibrosis and periportal hepatocytes with glycogenated nuclei |
4 | 35 | F | Wilson's d. | Focal steatosis, periportal and septal fibrosis |
5 | 36 | F | Wilson's d. | Mild nonspecific hepatocellular injury with spotty hepatocyte necrosis and mononuclear portal |
inflammatory infiltrate, scattered apoptotic bodies and mild steatosis | ||||
6 | 29 | M | AIH type I | Portal and lobular inflammation, periportal fibrosis |
7 | 33 | F | AIH type I | Portal and periportal inflammation, spotty necrosis |
8 | 33 | F | AIH type I | Chronic hepatitis pattern of injury with portal-based inflammation and fibrosis |
9 | 40 | F | AIH type I | Periportal interface activity and scattered hepatocyte necrosis |
10 | 35 | F | PBC | Bile duct injury with epithelioid granuloma, portal inflammation |
11 | 32 | M | Toxic hepatitis | Portal inflammation with scattered eosinophils, spotty necrosis |
12 | 50 | F | Budd-Chiari s. | Extensive centrilobular necrosis of hepatocytes |
13 | 22 | M | Celiac hepatitis | Non-specific reactive hepatitis with mild portal inflammation |
14 | 27 | M | Celiac hepatitis | Mild lobular inflammation with apoptotic bodies and hepatocyte necrosis |
15 | 50 | F | Celiac hepatitis | Mild periportal fibrosis with mild portal inflammation and focal interface activity |
16 | 40 | F | NASH | Ballooned hepatocytes, macrovesicular steatosis accentuated in zone 3 without significant liver injury |
- Citation: Drastich P, Honsová E, Lodererová A, Jarešová M, Pekáriková A, Hoffmanová I, Tučková L, Tlaskalová-Hogenová H, Špičák J, Sánchez D. Celiac disease markers in patients with liver diseases: A single center large scale screening study. World J Gastroenterol 2012; 18(43): 6255-6262
- URL: https://www.wjgnet.com/1007-9327/full/v18/i43/6255.htm
- DOI: https://dx.doi.org/10.3748/wjg.v18.i43.6255