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Aetiological differences in demographical, clinical and pathological characteristics of hepatocellular carcinoma in The Gambia

Background: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, with a high burden in West Africa. Data evaluating aetiological differences in HCC presentation from this region are limited. Aims: The aim of this study was to describe the demographical, clinical and patho...

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Published in:Liver international 2011-02, Vol.31 (2), p.215-221
Main Authors: Umoh, Nsikak J., Lesi, Olufunmilayo A., Mendy, Maimuna, Bah, Ebrima, Akano, Aliu, Whittle, Hilton, Hainaut, Pierre, Kirk, Gregory D.
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container_issue 2
container_start_page 215
container_title Liver international
container_volume 31
creator Umoh, Nsikak J.
Lesi, Olufunmilayo A.
Mendy, Maimuna
Bah, Ebrima
Akano, Aliu
Whittle, Hilton
Hainaut, Pierre
Kirk, Gregory D.
description Background: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, with a high burden in West Africa. Data evaluating aetiological differences in HCC presentation from this region are limited. Aims: The aim of this study was to describe the demographical, clinical and pathological characteristics of HCC by aetiology (hepatitis B or C infection, aflatoxin associated). Methods: One hundred and ninty‐three cases of HCC diagnosed between 1997 and 2001 in The Gambia were analysed. Characteristics were compared by aetiology using χ2‐tests, student t‐test and Wilcoxon's rank sum tests as appropriate. Results: The prevalence of hepatitis B surface antigen, hepatitis C antibody and aflatoxin‐associated 249serTP53 mutations among HCC patients was 60, 20 and 38% respectively. The typical HCC patient was a 49‐year‐old male positive for hepatitis B surface antigen presenting with hepatomegaly (93%), abdominal pain (94%) and weight loss (95%) 8 weeks after symptom onset. Most patients had multifocal lesions with background cirrhosis. The median largest tumour was 10.3 cm and the median α‐fetoprotein level was 500 ng/ml. Eighty‐four per cent of patients had advanced HCC (patients not meeting the Milan criteria) at presentation. Conclusions: Irrespective of aetiological agent, HCC among West Africans presents at very advanced stages. Few clinical or pathological differences exist by aetiology. More studies are needed to understand the mechanisms of hepatocarcinogenesis among these patients as well as identify high‐risk populations in which early detection through screening will be beneficial.
doi_str_mv 10.1111/j.1478-3231.2010.02418.x
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Data evaluating aetiological differences in HCC presentation from this region are limited. Aims: The aim of this study was to describe the demographical, clinical and pathological characteristics of HCC by aetiology (hepatitis B or C infection, aflatoxin associated). Methods: One hundred and ninty‐three cases of HCC diagnosed between 1997 and 2001 in The Gambia were analysed. Characteristics were compared by aetiology using χ2‐tests, student t‐test and Wilcoxon's rank sum tests as appropriate. Results: The prevalence of hepatitis B surface antigen, hepatitis C antibody and aflatoxin‐associated 249serTP53 mutations among HCC patients was 60, 20 and 38% respectively. The typical HCC patient was a 49‐year‐old male positive for hepatitis B surface antigen presenting with hepatomegaly (93%), abdominal pain (94%) and weight loss (95%) 8 weeks after symptom onset. Most patients had multifocal lesions with background cirrhosis. The median largest tumour was 10.3 cm and the median α‐fetoprotein level was 500 ng/ml. Eighty‐four per cent of patients had advanced HCC (patients not meeting the Milan criteria) at presentation. Conclusions: Irrespective of aetiological agent, HCC among West Africans presents at very advanced stages. Few clinical or pathological differences exist by aetiology. More studies are needed to understand the mechanisms of hepatocarcinogenesis among these patients as well as identify high‐risk populations in which early detection through screening will be beneficial.</description><identifier>ISSN: 1478-3223</identifier><identifier>EISSN: 1478-3231</identifier><identifier>DOI: 10.1111/j.1478-3231.2010.02418.x</identifier><identifier>PMID: 21143369</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; aflatoxin ; Aflatoxin B1 - toxicity ; Aged ; Carcinoma, Hepatocellular - epidemiology ; Carcinoma, Hepatocellular - etiology ; Carcinoma, Hepatocellular - pathology ; Demography ; Female ; Gambia - epidemiology ; Hepatitis B - complications ; Hepatitis B - epidemiology ; Hepatitis B Surface Antigens - analysis ; hepatitis B virus ; Hepatitis C - complications ; Hepatitis C - epidemiology ; Hepatitis C Antigens - analysis ; hepatitis C virus ; hepatocellular carcinoma ; Humans ; Liver Neoplasms - epidemiology ; Liver Neoplasms - etiology ; Liver Neoplasms - pathology ; Male ; Middle Aged ; Mutation, Missense - genetics ; Prevalence ; Sex Factors ; Tumor Suppressor Protein p53 - genetics</subject><ispartof>Liver international, 2011-02, Vol.31 (2), p.215-221</ispartof><rights>2010 John Wiley &amp; Sons A/S</rights><rights>2010 John Wiley &amp; Sons A/S.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3578-b696582fee0a6533db19a7a4d495dd8e29a996c3d1510888c46db339a1a9a6473</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21143369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Umoh, Nsikak J.</creatorcontrib><creatorcontrib>Lesi, Olufunmilayo A.</creatorcontrib><creatorcontrib>Mendy, Maimuna</creatorcontrib><creatorcontrib>Bah, Ebrima</creatorcontrib><creatorcontrib>Akano, Aliu</creatorcontrib><creatorcontrib>Whittle, Hilton</creatorcontrib><creatorcontrib>Hainaut, Pierre</creatorcontrib><creatorcontrib>Kirk, Gregory D.</creatorcontrib><title>Aetiological differences in demographical, clinical and pathological characteristics of hepatocellular carcinoma in The Gambia</title><title>Liver international</title><addtitle>Liver Int</addtitle><description>Background: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, with a high burden in West Africa. Data evaluating aetiological differences in HCC presentation from this region are limited. Aims: The aim of this study was to describe the demographical, clinical and pathological characteristics of HCC by aetiology (hepatitis B or C infection, aflatoxin associated). Methods: One hundred and ninty‐three cases of HCC diagnosed between 1997 and 2001 in The Gambia were analysed. Characteristics were compared by aetiology using χ2‐tests, student t‐test and Wilcoxon's rank sum tests as appropriate. Results: The prevalence of hepatitis B surface antigen, hepatitis C antibody and aflatoxin‐associated 249serTP53 mutations among HCC patients was 60, 20 and 38% respectively. The typical HCC patient was a 49‐year‐old male positive for hepatitis B surface antigen presenting with hepatomegaly (93%), abdominal pain (94%) and weight loss (95%) 8 weeks after symptom onset. Most patients had multifocal lesions with background cirrhosis. The median largest tumour was 10.3 cm and the median α‐fetoprotein level was 500 ng/ml. Eighty‐four per cent of patients had advanced HCC (patients not meeting the Milan criteria) at presentation. Conclusions: Irrespective of aetiological agent, HCC among West Africans presents at very advanced stages. Few clinical or pathological differences exist by aetiology. More studies are needed to understand the mechanisms of hepatocarcinogenesis among these patients as well as identify high‐risk populations in which early detection through screening will be beneficial.</description><subject>Adult</subject><subject>aflatoxin</subject><subject>Aflatoxin B1 - toxicity</subject><subject>Aged</subject><subject>Carcinoma, Hepatocellular - epidemiology</subject><subject>Carcinoma, Hepatocellular - etiology</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Demography</subject><subject>Female</subject><subject>Gambia - epidemiology</subject><subject>Hepatitis B - complications</subject><subject>Hepatitis B - epidemiology</subject><subject>Hepatitis B Surface Antigens - analysis</subject><subject>hepatitis B virus</subject><subject>Hepatitis C - complications</subject><subject>Hepatitis C - epidemiology</subject><subject>Hepatitis C Antigens - analysis</subject><subject>hepatitis C virus</subject><subject>hepatocellular carcinoma</subject><subject>Humans</subject><subject>Liver Neoplasms - epidemiology</subject><subject>Liver Neoplasms - etiology</subject><subject>Liver Neoplasms - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation, Missense - genetics</subject><subject>Prevalence</subject><subject>Sex Factors</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><issn>1478-3223</issn><issn>1478-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNo9kU1v1DAQhi0Eoh_wF5BvXNgltmPHPnCoqnZbaQUILe3RmtiTxks-Fjurbi_97STdEl888jzvaPy-hFCWLdl4vm6XLC_0QnDBljwbXzOeM708vCGnc-PtXHNxQs5S2mYZM0ay9-SEM5YLocwpeb7AIfRN_xAcNNSHqsKIncNEQ0c9tv1DhF09Nb9Q14TuBYPO0x0M9axzNURwA8aQhuAS7Sta40j0Dptm30CkDqILXd_CNHdTI11BWwb4QN5V0CT8-Hqfk9_XV5vLm8X6x-r28mK9cEKOfyiVUVLzCjEDJYXwJTNQQO5zI73XyA0Yo5zwTLJMa-1y5UshDDAwoPJCnJPPx7m72P_dYxpsG9K0HHTY75PVnEspeW5G8tMruS9b9HYXQwvxyf63bAS-HYHH0ODT3GeZnaKxWzu5bqcE7BSNfYnGHuz69m6qRv3iqB-9wsOsh_jHqkIU0t5_X9mf6nqjC_bLCvEP8VySbg</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Umoh, Nsikak J.</creator><creator>Lesi, Olufunmilayo A.</creator><creator>Mendy, Maimuna</creator><creator>Bah, Ebrima</creator><creator>Akano, Aliu</creator><creator>Whittle, Hilton</creator><creator>Hainaut, Pierre</creator><creator>Kirk, Gregory D.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201102</creationdate><title>Aetiological differences in demographical, clinical and pathological characteristics of hepatocellular carcinoma in The Gambia</title><author>Umoh, Nsikak J. ; Lesi, Olufunmilayo A. ; Mendy, Maimuna ; Bah, Ebrima ; Akano, Aliu ; Whittle, Hilton ; Hainaut, Pierre ; Kirk, Gregory D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3578-b696582fee0a6533db19a7a4d495dd8e29a996c3d1510888c46db339a1a9a6473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>aflatoxin</topic><topic>Aflatoxin B1 - toxicity</topic><topic>Aged</topic><topic>Carcinoma, Hepatocellular - epidemiology</topic><topic>Carcinoma, Hepatocellular - etiology</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Demography</topic><topic>Female</topic><topic>Gambia - epidemiology</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B - epidemiology</topic><topic>Hepatitis B Surface Antigens - analysis</topic><topic>hepatitis B virus</topic><topic>Hepatitis C - complications</topic><topic>Hepatitis C - epidemiology</topic><topic>Hepatitis C Antigens - analysis</topic><topic>hepatitis C virus</topic><topic>hepatocellular carcinoma</topic><topic>Humans</topic><topic>Liver Neoplasms - epidemiology</topic><topic>Liver Neoplasms - etiology</topic><topic>Liver Neoplasms - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation, Missense - genetics</topic><topic>Prevalence</topic><topic>Sex Factors</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Umoh, Nsikak J.</creatorcontrib><creatorcontrib>Lesi, Olufunmilayo A.</creatorcontrib><creatorcontrib>Mendy, Maimuna</creatorcontrib><creatorcontrib>Bah, Ebrima</creatorcontrib><creatorcontrib>Akano, Aliu</creatorcontrib><creatorcontrib>Whittle, Hilton</creatorcontrib><creatorcontrib>Hainaut, Pierre</creatorcontrib><creatorcontrib>Kirk, Gregory D.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Liver international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Umoh, Nsikak J.</au><au>Lesi, Olufunmilayo A.</au><au>Mendy, Maimuna</au><au>Bah, Ebrima</au><au>Akano, Aliu</au><au>Whittle, Hilton</au><au>Hainaut, Pierre</au><au>Kirk, Gregory D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aetiological differences in demographical, clinical and pathological characteristics of hepatocellular carcinoma in The Gambia</atitle><jtitle>Liver international</jtitle><addtitle>Liver Int</addtitle><date>2011-02</date><risdate>2011</risdate><volume>31</volume><issue>2</issue><spage>215</spage><epage>221</epage><pages>215-221</pages><issn>1478-3223</issn><eissn>1478-3231</eissn><abstract>Background: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, with a high burden in West Africa. Data evaluating aetiological differences in HCC presentation from this region are limited. Aims: The aim of this study was to describe the demographical, clinical and pathological characteristics of HCC by aetiology (hepatitis B or C infection, aflatoxin associated). Methods: One hundred and ninty‐three cases of HCC diagnosed between 1997 and 2001 in The Gambia were analysed. Characteristics were compared by aetiology using χ2‐tests, student t‐test and Wilcoxon's rank sum tests as appropriate. Results: The prevalence of hepatitis B surface antigen, hepatitis C antibody and aflatoxin‐associated 249serTP53 mutations among HCC patients was 60, 20 and 38% respectively. The typical HCC patient was a 49‐year‐old male positive for hepatitis B surface antigen presenting with hepatomegaly (93%), abdominal pain (94%) and weight loss (95%) 8 weeks after symptom onset. Most patients had multifocal lesions with background cirrhosis. The median largest tumour was 10.3 cm and the median α‐fetoprotein level was 500 ng/ml. Eighty‐four per cent of patients had advanced HCC (patients not meeting the Milan criteria) at presentation. Conclusions: Irrespective of aetiological agent, HCC among West Africans presents at very advanced stages. Few clinical or pathological differences exist by aetiology. More studies are needed to understand the mechanisms of hepatocarcinogenesis among these patients as well as identify high‐risk populations in which early detection through screening will be beneficial.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21143369</pmid><doi>10.1111/j.1478-3231.2010.02418.x</doi><tpages>7</tpages></addata></record>
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ispartof Liver international, 2011-02, Vol.31 (2), p.215-221
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subjects Adult
aflatoxin
Aflatoxin B1 - toxicity
Aged
Carcinoma, Hepatocellular - epidemiology
Carcinoma, Hepatocellular - etiology
Carcinoma, Hepatocellular - pathology
Demography
Female
Gambia - epidemiology
Hepatitis B - complications
Hepatitis B - epidemiology
Hepatitis B Surface Antigens - analysis
hepatitis B virus
Hepatitis C - complications
Hepatitis C - epidemiology
Hepatitis C Antigens - analysis
hepatitis C virus
hepatocellular carcinoma
Humans
Liver Neoplasms - epidemiology
Liver Neoplasms - etiology
Liver Neoplasms - pathology
Male
Middle Aged
Mutation, Missense - genetics
Prevalence
Sex Factors
Tumor Suppressor Protein p53 - genetics
title Aetiological differences in demographical, clinical and pathological characteristics of hepatocellular carcinoma in The Gambia
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