HEPATOCELLULAR-CARCINOMA AND NODULAR REGENERATIVE HYPERPLASIA - POSSIBLE PATHOGENETIC RELATIONSHIP

Citation
Uc. Nzeako et al., HEPATOCELLULAR-CARCINOMA AND NODULAR REGENERATIVE HYPERPLASIA - POSSIBLE PATHOGENETIC RELATIONSHIP, The American journal of gastroenterology, 91(5), 1996, pp. 879-884
Citations number
19
Categorie Soggetti
Gastroenterology & Hepatology
ISSN journal
00029270
Volume
91
Issue
5
Year of publication
1996
Pages
879 - 884
Database
ISI
SICI code
0002-9270(1996)91:5<879:HANRH->2.0.ZU;2-E
Abstract
Objective: In a recent review of hepatocellular carcinoma (HCC) in Nor th American residents, we were surprised to learn that 42.6% of these tumors in the 1980-1993 consultation files of the Armed Forces Institu te of Pathology had arisen in noncirrhotic livers. We subsequently not ed that the nonneoplastic livers of a number of these had nodular rege nerative hyperplasia (NRH), a condition that has been associated with liver cell dysplasia, a putative premalignant lesion. To investigate t he possibility that NRH might be a precursor of HCC, we studied those cases in which there was an association of HCC and NRH and examined th e possible role of portal vein obstruction in NRH occurring in livers with HCC. Methods: Subjects were selected based on study criteria and histological slides, clinical/autopsy records were reviewed, and featu res of neoplastic and nonneoplastic liver were noted. Simple statistic al comparisons were made between the groups with and without NRH with respect to defined variables. Results: Of 804 patients suitable for st udy, 342 were noncirrhotic, and 23 of these had NRH. Mean age of patie nts with NRH was 65 +/- 13.6 (SD) yr. Seventeen of these (73.9%) had l iver cell dysplasia, and 16 (69.6%) had portal venous invasion. Liver cell dysplasia occurred in a significantly greater proportion of those with NRH than those without (p < 0.01), but there was no significant difference between both groups with regard to portal venous invasion. Three patients (13%) had received chemotherapy and/or radiotherapy bef ore diagnosis of NRH. Conclusions: These findings may be due to the de velopment of HCC within the dysplastic foci that occur in livers with NRH, but the findings do not exclude the converse possibility that NRH may also develop in a noncirrhotic liver with HCC, secondary to porta l venous invasion with portal vein occlusion. The temporal relationshi p between HCC and NRH is probably determined in each case by the parti cular interaction of multiple pathogenetic factors. Among patients wit h HCC, factors other than portal vein obstruction by tumor invasion ma y play a role in the pathogenesis of NRH.