Can large cell change and high proliferative activity predict hepatocellular carcinoma in patients with hereditary hemochromatosis?

被引:7
作者
Fracanzani, AL
Borzio, M
Roncalli, M
Derenzini, M
Treré, D
Mattioli, M
Taioli, E
Fiorelli, G
Fargion, S
机构
[1] Univ Milan, Dipartimento Med Interna, Osped Maggiore IRCCS, I-20122 Milan, Italy
[2] Osped Fatebenefratelli, Div Med 1, Milan, Italy
[3] Univ Milan, Ist Clin Hunamitas, Ist Anat Patol, I-20122 Milan, Italy
[4] Univ Bologna, Dipartimento Patol Sperimentale, I-40126 Bologna, Italy
[5] Osped Maggiore IRCCS, Unita Epidemiol, Milan, Italy
关键词
D O I
10.1016/S0002-9270(00)01118-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVE: Patients with hereditary hemochromatosis are at high risk of developing hepatocellular carcinoma. This study was undertaken to define whether large cell change and nucleolar organizer regions proliferative index (marker of high proliferative activity) predict hepatocellular carcinoma development in hereditary hemochromatosis. METHODS: Histological staining for large cell change and high proliferative activity were done on baseline liver biopsies of 74 patients with hereditary hemochromatosis (52 with and 22 without cirrhosis), prospectively followed-up for 83 +/- 53 months (range, 1-230 months). RESULTS: Large cell change and high proliferative activity were found only in cirrhotic patients; 16 of 52 patients (31%) had either the large cell change or high proliferative activity. Large cell change was more frequent in patients with hepatitis B surface antigen than in those positive for hepatitis C virus (57% vs 14%, p = 0.04). Hepatocellular carcinoma developed in 7 of 16 (44%) and in 6 of 36 patients (16%) of the patients positive or negative for these morphological variables. The probability of developing hepatocellular carcinoma at 7 yr of follow-up was significantly higher in patients with large cell change or high proliferative activity than in those without. The length of follow-up from baseline histology to hepatocellular carcinoma occurrence was shorter in patients with large cell change or high proliferative activity than in those without these changes (46 +/- 36 and 109 +/- 34 months, p = 0.01). A multivariate analysis indicated that in patients with cirrhosis, large cell change or high proliferative activity (considered as a single variable), and age >55 yr were the only independent variables significantly associated with the risk of,developing hepatocellular carcinoma, with a risk ratio of 4.8 (confidence interval 1.2-18.2) and 4.0 (confidence interval 1.1-15.6), respectively. CONCLUSIONS: In hereditary hemochromatosis, the presence of large cell change or high proliferative activity in patients older than 55 yr with cirrhosis should be considered a strong predictor of hepatocellular carcinoma development, especially if hepatitis B virus infection coexists. (Am J Gastroenterol 2000;95:2940-2945. (C) 2000 by Am. Coll. of Gastroenterology).
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页码:2940 / 2945
页数:6
相关论文
共 39 条
[1]
LIVER-CELL DYSPLASIA - PREMALIGNANT CONDITION [J].
ANTHONY, PP ;
VOGEL, CL ;
BARKER, LF .
JOURNAL OF CLINICAL PATHOLOGY, 1973, 26 (03) :217-223
[2]
Premalignant lesions and hepatocellular carcinoma in a non-cirrhotic alcoholic patient with iron overload and normal transferrin saturation [J].
Blanc, JF ;
De Ledinghen, V ;
Trimoulet, P ;
Le Bail, B ;
Bernard, PH ;
Saric, J ;
Balabaud, C ;
Bioulac-Sage, P .
JOURNAL OF HEPATOLOGY, 1999, 30 (02) :325-329
[3]
Borzio M, 1998, J CLIN PATHOL-MOL PA, V51, P96
[4]
LIVER-CELL DYSPLASIA IS A MAJOR RISK FACTOR FOR HEPATOCELLULAR-CARCINOMA IN CIRRHOSIS - A PROSPECTIVE-STUDY [J].
BORZIO, M ;
BRUNO, S ;
RONCALLI, M ;
MELS, GC ;
RAMELLA, G ;
BORZIO, F ;
LEANDRO, G ;
SERVIDA, E ;
PODDA, M .
GASTROENTEROLOGY, 1995, 108 (03) :812-817
[5]
HEPATOCELLULAR-CARCINOMA IN ITALIAN PATIENTS WITH CIRRHOSIS [J].
COLOMBO, M ;
DEFRANCHIS, R ;
DELNINNO, E ;
SANGIOVANNI, A ;
DEFAZIO, C ;
TOMMASINI, M ;
DONATO, MF ;
PIVA, A ;
DICARLO, V ;
DIOGUARDI, N .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (10) :675-680
[6]
COX DR, 1972, J R STAT SOC B, V34, P187
[7]
IS HIGH AGNOR QUANTITY IN HEPATOCYTES ASSOCIATED WITH INCREASED RISK OF HEPATOCELLULAR-CARCINOMA IN CHRONIC LIVER-DISEASE [J].
DERENZINI, M ;
TRERE, D ;
OLIVERI, F ;
DAVID, E ;
COLOMBATTO, P ;
BONINO, F ;
BRUNETTO, MR .
JOURNAL OF CLINICAL PATHOLOGY, 1993, 46 (08) :727-729
[8]
ULTRASTRUCTURAL CYTOCHEMISTRY OF THE MAMMALIAN-CELL NUCLEOLUS [J].
DERENZINI, M ;
THIRY, M ;
GOESSENS, G .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1990, 38 (09) :1237-1256
[9]
PRENEOPLASTIC SIGNIFICANCE OF HEPATIC IRON-FREE FOCI IN GENETIC HEMOCHROMATOSIS - A STUDY OF 185 PATIENTS [J].
DEUGNIER, YM ;
CHARALAMBOUS, P ;
LEQUILLEUC, D ;
TURLIN, B ;
SEARLE, J ;
BRISSOT, P ;
POWELL, LW ;
HALLIDAY, JW .
HEPATOLOGY, 1993, 18 (06) :1363-1369
[10]
PRIMARY LIVER-CANCER IN GENETIC HEMOCHROMATOSIS - A CLINICAL, PATHOLOGICAL, AND PATHOGENETIC STUDY OF 54 CASES [J].
DEUGNIER, YM ;
GUYADER, D ;
CRANTOCK, L ;
LOPEZ, JM ;
TURLIN, B ;
YAOUANQ, J ;
JOUANOLLE, H ;
CAMPION, JP ;
LAUNOIS, B ;
HALLIDAY, JW ;
POWELL, LW ;
BRISSOT, P .
GASTROENTEROLOGY, 1993, 104 (01) :228-234