Liver cell dysplasia (LCD) is considered a preneoplastic that LCD is a premalignant lesion is still controversial. Most studies favor the premalignant nature of LCD, but some critilesion, whose characterization and differentiation from hepatocellular carcinoma (HCC) and from the reactive changes cize this concept and have indicated that there is no proven causal relationship between LCD and hepatocellular carciseen in cirrhosis has been controversial. We studied 12 cases of LCD (large cell type) with image analysis techniques (IA) noma (HCC), either enzymatically or by karyometric analysis, and that LCD represents only regenerative or degeneraand compared the findings with those of HCC (n Å 40), and a spectrum of non-neoplastic hepatic lesions including normal tive alterations.1-5 In Anthony's original study of 552 Ugandan patients with normal, cirrhotic, and cancerous livliver and cirrhosis (n Å 49). A minimum of 200 Feulgenstained nuclei were measured from each lesion with the CAS ers, LCD was seen in 1% of otherwise normal livers, 7%of livers with HCC without cirrhosis, 20% of patients with 200 image analysis system. The data were collected with the aid of CellSheet software. Thirty-four variables were mea-cirrhosis without carcinoma, and in 65% of livers of patients who had HCC in the setting of cirrhosis. 1 Anthony et al. also sured, including geometric, textural, and photometric nuclear features and DNA ploidy. The data were analyzed with multi-demonstrated a high association of LCD with macronodular cirrhosis, male sex, and serum hepatitis B antigen positivvariate statistics and a backpropagation neural network (NN). Stepwise statistical analysis selected 22 variables that were ity.1,2 A similar relationship between hepatocellular dysplasia and the presence of hepatitis B surface antigen (HBsAg) sestatistically significant in the three groups with P values õ.05. Various NN architectures were developed using these vari-rum positivity has also been demonstrated by Nakashima 6 and Roncalli.7 However, LCD has been shown to occur in ables. The best NN architecture included a sigmoidal transfer function, 14 input, 16 hidden, and 3 output neurons. It trained the absence of serum HBsAg.8 LCD can also be associated with chronic hepatitis C virus infection.
9,10to completion after 8,887 runs using 90% of the lesions. This NN yielded a 100% cross-validation rate for unknown cases.A variety of special techniques have been used to study LCD, including immunohistochemistry for hepatitis B virus, These data support the concept of LCD (large cell type) as a lesion that can be objectively distinguished from HCC and a-fetoprotein, carcinoembryonic antigen, a 1 -antitrypsin, the proto-oncogene bcl-2, p53 protein, and the proliferating cell non-neoplastic liver. Our study also demonstrates the potential usefulness of IA for the evaluation of difficult histopatho-nuclear antigen (PCNA). 3,4,[11][12][13][14][15][16] Morphometric analysis and DNA cytometry have also been performed. 4,5,[17][18][19][20][21][22] These studlogical...