<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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<journal-meta>
<journal-id>0121-0793</journal-id>
<journal-title><![CDATA[Iatreia]]></journal-title>
<abbrev-journal-title><![CDATA[Iatreia]]></abbrev-journal-title>
<issn>0121-0793</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Antioquia]]></publisher-name>
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<article-meta>
<article-id>S0121-07932007000500012</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Epidemiology of hepatocellular carcinoma]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[PARANÁ]]></surname>
<given-names><![CDATA[RAYMUNDO]]></given-names>
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<name>
<surname><![CDATA[ALMEIDA]]></surname>
<given-names><![CDATA[DELVONE]]></given-names>
</name>
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<aff id="A01">
<institution><![CDATA[,Federal University of Bahia Associate Professor ]]></institution>
<addr-line><![CDATA[Salvador de Bahia ]]></addr-line>
<country>Brazil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2007</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2007</year>
</pub-date>
<volume>20</volume>
<fpage>s25</fpage>
<lpage>s28</lpage>
<copyright-statement/>
<copyright-year/>
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</front><body><![CDATA[ <p ><font size="4"><b>Epidemiology of hepatocellular       carcinoma</b></font></p>       <p ><font size="2">RAYMUNDO PARAN&Aacute; AND  DELVONE  ALMEIDA<sup>1</sup></font></p>   <ol>    <li><font size="2">Associate       Professor, Federal University of Bahia, Salvador de Bahia, Brazil. <a href="mailto:unif@svn.com.br">unif@svn.com.br</a></font></li>     </ol>   <hr>       <p ><b><font size="2">INTRODUCTION.</font></b><font size="2"> The incidence of hepatocellular carcinoma (HCC)       has increased both due to the worldwide increase on the virus C infection       and to the increase on the survival rate of patients with chronic liver       disease.</font></p>       <p ><font size="2">It usually       is an aggressive tumor with survival rate directly associated with the       hepatic residual liver function as well as the size of the tumor at the       diagnosis.</font></p>       <p ><font size="2">Despite occupying       the 7th position among malignant neoplasies worldwide, it is currently       considered as the 3rd cause of death due to cancer occurring most frequently       among men than among women (3:1) and between the 6th and 7th decades of       life. In hyperendemic regions for the hepatitis B virus (HBV), it occurs       in younger individuals, between the 3rd and 5th decades of life <sup>1</sup>.</font></p>       <p ><font size="2">About 60       &#150; 80% of patients with HCC present liver cirrhosis <sup>2</sup>. Because of this association the treatment       of this tumor is a challenge for the modern hepatology, since it presents       poor response to chemotherapic agents. The surgical and non&#150;surgical ablation       methods depend on factors inherent not only to the tumor itself but also       to the etiology and stage of liver disease.</font></p>       <p ><font size="2"><b>HCC ETIOLOGY  AND EPIDEMIOLOGY.</b> Usually,       the liver structural alterations occur along the years, before HCC develops       in the hepatic tissue. The HCC diagnosis may be verified in individuals       with no known previous history of liver disease; however, this diagnosis       will be coincident with biochemical and laboratorial evidences of hepatocellular       dysfunction or viral infection, besides metabolic disorders of associated       diseases, making HCC the starting point for the hepatic disease diagnosis.       However, in patients under screening, HCC may be detected in early phases,       with better prognosis. The HCC development in normal livers is unusual;       thus, the HCC epidemiology will be established based on its etiological       factors.</font></p>       <p ><font size="2"><b>HEPATITIS B VIRUS (HBV).</b> Approximately 400 million       people worldwide are chronic hepatitis carriers. Over       than 40% of these patients will develop serious hepatic complications such       as the HCC. </font></p>       ]]></body>
<body><![CDATA[<p ><font size="2">The hepatitis       B is present in all continents. There is a variability of infection rates       in function of the different regions of the globe (from 0.1% to 20%). Therefore,       the different regions of the world are divided into high endemicity, intermediate       endemicity and low endemicity areas.</font></p>       <p ><font size="2">In low endemicity       areas, the prevalence of chronic HBV carriers is lower than 2%. In intermediate       endemicity areas, the prevalence of chronic HBV carriers ranges from 2%       to 7% and from 20% to 50% of the population have serological evidence of       past infection. The highest infection rates are among older children, adolescents       and young adults. Intermediate prevalence regions include Eastern Europe       countries such as Russia, countries from the Mediterranean basin, Southeastern       Asia, Japan and Northern Latin America.</font></p>       <p ><font size="2">In high endemicity       areas, the risk of HBV infection is higher than 60% and most infections       occur at birth or early in the childhood. All children from this population       present high risk of acquiring chronic infection before the age of 5 years.       In these areas, the rate of chronic HBV carriers ranges from 8% to 25%       and the antiHBs prevalence is arround 60 to 85%.</font></p>       <p ><font size="2">Since the       implementation of HBV vaccination in counties from North America and Europe       from 1985 on, a significant reduction on the number of new cases in those       regions was documented. However, the continuous immigration of from endemic       regions (Asia and Africa) reveals that viral reservoirs persist in these       areas, what makes crucial the continuous disease surveillance l <sup>4</sup>.</font></p>       <p ><font size="2">Approximately       5 &#150; 10% of infected adult individuals become chronic, and may evoluate       toward advanced liver disease and hepatocellular carcinoma. HBV carriers       present a risk 100 times higher than normal individuals of developing hepatocellular       carcinoma (HCC). About 60 &#150; 80% of HCC cases detected worldwide are associated       with HBV <sup>5</sup>.</font></p>       <p ><font size="2"><b>HEPATITIS C VIRUS (HCV).</b> It is estimated that about 175 million people         are infected with the HCV worldwide. The mortality rate associated to         the HCV will increase two or three times in the next decades in infected         patients who develop cirrhosis and will become the greatest indication         of liver transplantation.</font></p>       <p ><font size="2">Two zones       of HCV prevalence may be defined based on data obtained from world blood       banks: the zone of strong prevalence, with 0.5 to 1.5% of blood donors       includes Japan, Spain, Hungary, Southeastern Italy, Africa, Asia and South       America. Egypt presents the highest prevalence, between 10% and 30% <sup>6</sup>. The zone       of low prevalence, with 0.001 to 0.05% of blood donors includes European       countries, USA and Canada.</font></p>       <p ><font size="2">It is also       estimated the 10 &#150; 20% of patients with chronic hepatitis due to HCV at       cirrhosis stage may develop HCC within ten years of disease evolution.       The carcinogenesis mechanisms are not yet fully elucidated. Since it deals       about a RNA&#150;type virus, it cannot integrate to the hepatocyte genome. It       has been postulated that the HCV core protein presents oncogenic properties <sup>7</sup>. It is believed       that the presence of cirrhosis is a preponderant factor for HCV emergence       in HCV carriers <sup>8</sup>. An asiat study demonstrated       that 25% of patients at cirrhosis stage developed HCC within five years <sup>9</sup>.</font></p>       <p ><font size="2"><b>ALCOHOL AND AFLATOXIN.</b> Alcohol is associated with digestive tract cancer         such as esophagus and pancreas (alcohol&#150;induced chronic pancreatitis).         The alcohol intake in HBV or HCV carriers can induce the fibrosis progression         and hence to hepatic carcinogenesis.</font></p>       <p ><font size="2">The Aflatoxin,       a toxin produced by the  <em>Aspergillus fungus</em>, may contaminate stored food such as peanuts, soybeans and rice, and is, at       least, partially responsible for the development of HCC among some populations       from Africa and China <sup>10</sup>.</font></p>       ]]></body>
<body><![CDATA[<p ><font size="2"><b>METABOLIC   AND HEREDITARY DISEASES.</b> Other hepatic diseases, among which, autoimmune         hepatitis, hemochromatosis, Wilson disease, alpha&#150;1 antitrypsin deficiency         and primary biliary cirrhosis may be associated to the HCC development,         when in cirrhosis stage. The HCC incidence in the hemochromatosis seems         to be higher than in other metabolic diseases <sup>11</sup>.</font></p>       <p ><font size="2"><b>STUDIES ASSOCIATED TO THE HCC EPIDEMIOLOGY.</b> The geographic       distribution of HCC coincides with the epidemiology of hepatotropic viruses       such as HBV and HCV, as mentioned before. The most recent epidemiological       studies corroborate this characteristic. In Canada, ElSaadany &amp; Giulivi       (2006) <sup>12</sup> evaluated 403 cases       of HCC and found that 15% of cases were associated hepatitis (B and C)       and 22% to alcohol. Dissimilarly, Abdel&#150;Whab et. al (2007) <sup>13</sup> in Egypt,       found HCV as etiologic factor for HCC in 76.6% of cases and B virus in       3.3% of cases. Southeastern Asia, Japan and South Africa present high HCC       incidence, what is coincident with the high HBV prevalence.</font></p>       <p ><font size="2">In Brazil,       according to data from the National Cancer Institute (Inca), the HCC rate       per each 100 thousand inhabitants is different from state to state, being       of 1.07 (males only) in Belém (Eastern Amazonia) in the year of 1988 and       9.34 in Porto Alegre (South) in 1991. However, there is still a lack of       data for the HCC epidemiological characterization, factor associated to       the difficulty of access to image and laboratorial exams that could clear       the diagnosis.</font></p>       <p ><font size="2"><b>REFERENCES</b></font></p>       <!-- ref --><p ><font size="2">1. PARIKH       S, HYMAN D. Hepatocellular carcinoma: a guide for the internist. American       Journal of Medicine, 120: 194&#150;202, 2007.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000027&pid=S0121-0793200700050001200001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p ><font size="2">2. OKUDA       K. Hepatocellular carcinoma. Journal of Hepatology, 32:225&#150;37, 2000.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000028&pid=S0121-0793200700050001200002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p ><font size="2">3. SHAPIRO       CN. Epidemiology of hepatitis B. 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In:       Hollinger FB, Lemon SM, Margolis H, eds Viral       Hepatitis and Liver Disease. Baltimore, MD: Williams and Wilkins, 289&#150;96p.,       1991.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000031&pid=S0121-0793200700050001200005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p ><font size="2">6. ALTER       HJ. Evaluation of second generation assays for detection of antibody to       the hepatitis C virus. Hepatology, 15: 350&#150;3, 1992.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000032&pid=S0121-0793200700050001200006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p ><font size="2">7. 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<person-group person-group-type="author">
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