TY - JOUR
T1 - Early stages of multistep hepatocarcinogenesis
T2 - Adenomatous hyperplasia and early hepatocellular carcinoma
AU - Sakamoto, Michiie
AU - Hirohashi, Setsuo
AU - Shimosato, Yukio
N1 - Funding Information:
From the Pathology Division, National Cancer Center Research Institute, Tokyo, Japan. Accepted for publication May 15, 1990. Supported in part by a Grant-in-Aid for Cancer Research (6Y-7) from the Ministry of Health and Welfare. Key uwnh: early hepatocellular carcinoma, preneoplastic sion, adenomatous hyperplasia, multistep hepatocarcinogenesis. Address correspondence and reprint requests to Setsuo Hiro-hashi, MD, Pathology Division, National Cancer Center Research Institute, 5-l-l Tsukiji, Chuo-ku, Tokyo 104, Japan. Copyright 0 1991 by W.B. Saunders Company 0046-S 17719 l/202-00 12$5.00/O
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1991/2
Y1 - 1991/2
N2 - From a series of 320 heptocellular carcinoma (HCC) cases treated surgically, we selected small nodular lesions that had not destroyed the preexisting liver structure grossly. After excluding metastases and large regenerative nodules, 58 lesions from 41 cases were chosen. All the lesions were hypercellular. Among them, 33 lesions showing histologic features of very well-differentiated HCC (Edmondson grade I), that is, small hepatocytes with little cellular atypia but with structural atypia, such as a thin trabecular structure of acinar formation in some areas, were classified as early HCC (eHCC). In seven eHCCs, areas of overt carcinoma, classified as Edmondson grade II, were found in the background of Edmondson grade I carcinoma. The remaining 25 lesions lacked structural atypia and were classified as adenomatous hyperplasia (AH). Among the AHs, 10 nodules with a very focal abnormal structure were subclassified as atypical adenomatous hyperplasia (AAH). There was a tendency for the size and cellularity of the atypical lesions to increase in order from AH to AAH to eHCC. All nodules larger than 1.5 cm were eHCC. A degree of cellularity more than twice that of a regenerative nodule was suggested to be an indicator of HCC. All small nodular lesions were associated with chronic liver disease. These histologic observations appear to explain the stepwise development of overt HCC from very well-differentiated eHCC, and of eHCC from AH probably through AAH, at least in cases of HCC associated with chronic liver disease.
AB - From a series of 320 heptocellular carcinoma (HCC) cases treated surgically, we selected small nodular lesions that had not destroyed the preexisting liver structure grossly. After excluding metastases and large regenerative nodules, 58 lesions from 41 cases were chosen. All the lesions were hypercellular. Among them, 33 lesions showing histologic features of very well-differentiated HCC (Edmondson grade I), that is, small hepatocytes with little cellular atypia but with structural atypia, such as a thin trabecular structure of acinar formation in some areas, were classified as early HCC (eHCC). In seven eHCCs, areas of overt carcinoma, classified as Edmondson grade II, were found in the background of Edmondson grade I carcinoma. The remaining 25 lesions lacked structural atypia and were classified as adenomatous hyperplasia (AH). Among the AHs, 10 nodules with a very focal abnormal structure were subclassified as atypical adenomatous hyperplasia (AAH). There was a tendency for the size and cellularity of the atypical lesions to increase in order from AH to AAH to eHCC. All nodules larger than 1.5 cm were eHCC. A degree of cellularity more than twice that of a regenerative nodule was suggested to be an indicator of HCC. All small nodular lesions were associated with chronic liver disease. These histologic observations appear to explain the stepwise development of overt HCC from very well-differentiated eHCC, and of eHCC from AH probably through AAH, at least in cases of HCC associated with chronic liver disease.
KW - adenomatous hyperplasia
KW - early hepatocellular carcinoma
KW - multistep hepatocarcinogenesis
KW - preneoplastic lesion
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U2 - 10.1016/0046-8177(91)90039-R
DO - 10.1016/0046-8177(91)90039-R
M3 - Article
C2 - 1848205
AN - SCOPUS:0026027904
SN - 0046-8177
VL - 22
SP - 172
EP - 178
JO - Human Pathology
JF - Human Pathology
IS - 2
ER -