Quantitation of Hepatic Granulomas and Epithelioid Cells in Primary Biliary Cirrhosis
β Scribed by Yasuni Nakanuma; Goroku Ohta
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 632 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
The number of granulomas and loosely arranged epithelioid cell foci in wedge liver biopsy specimens of 39 patients with primary biliary cirrhosis were counted and correlated with other hepatic lesions. Granulomas and cell foci were present in 76.9 and 87.2% of the patients, respectively; their numbers varied greatly from case to case (mean f S.D.: 2.4 k 3.4 per cm2 and 4.7 2 5.5 per cm2 of liver section; range: 0 to 18.5 per cm2 and 0 to 23.3 per cm2, respectively) and decreased as bile duct loss progressed. There was positive correlation between the number of cell foci with the extent of florid duct lesions, and negative correlation with hepatic fibrosis and deposition of copper granules.
Hepatic granulomas are associated with many types of liver disorders (1, 2) and are diagnostically useful in primary biliary cirrhosis (PBC) because of frequent occurrence around affected bile ducts (3) with or without a florid lesion. Typical granulomas occur in the liver of asymptomat,ic patients (4). Recently, PBC patients with hepatic granulomas were reported to have a better survival (5).
To evaluate the significance of the number of granulomas in PBC, a correlation study between the number of granulomas and other hepatic lesions, especially the degree of bile duct disappearance, was performed.
Methods
Wedge biopsies from 39 patients with histologic and clinical diagnosis of PBC (Table 1) were obtained from several institutions in Japan. The patients ranged from 28 to 70 years old; 37 were females. No patient had been treated with D-penicillamine or azathioprine before laparotomy for diagnostic surgical liver biopsy. Pruritus and/or jaundice were present in 20 cases. Antimitochondrial antibodies (AMAs) were found in 31 of 37 patients (83.8%). Eight patients, in whom AMAs were not detected, were diagnosed as PBC on the basis of clinical, laboratory, and morphologic findings: All livers showed chronic nonsuppurative destructive cholangitis and/or marked reduction in interlobular bile ducts (6-9).
π SIMILAR VOLUMES
Cluster of differentiation 1 (CD1) is a family of four distinct nonpolymorphic major histocompatibility complex class I-like molecules that can present microbial nonpeptide lipid antigens to T cells. Among the CD1 gene family, CD1d is found in a wide range of tissues including the intestine and live
Stellate cells have only recently received attention in patients with primary biliary cirrhosis (PBC). We have used electron microscopy and morphometry to perform a qualitative and quantitative examination of lipid-storing activity of stellate cells in liver biopsies of 26 patients with noncirrhotic
Primary biliary cirrhosis (PBC)-autoimmune hepatitis (AIH) overlap syndrome is a clinical entity characterized by the occurrence of both conditions at the same time in the same patient. In addition to PBC-AIH overlap syndrome, transitions from one autoimmune disease to another have been reported, bu