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      Hepatocellular carcinoma: clinicopathological profile and challenges of management in a resource-limited setting

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          Abstract

          Background

          Hepatocellular carcinoma is one of the most common cancers worldwide and its incidence is reported to be increasing in resource-limited countries. There is a paucity of published data regarding hepatocellular carcinoma in Tanzania, and the study area in particular. This study describes the clinicopathological profile of hepatocellular carcinoma in our local setting and highlights the challenging problems in the management of this disease.

          Methods

          This was a retrospective study of histopathologically confirmed cases of hepatocellular carcinoma seen at Bugando Medical Center between March 2009 and February 2013.

          Results

          A total of 142 patients (M: F = 2.2: 1) were studied representing 4.6% of all malignancies. The median age of patients was 45 years. Hepatitis B virus infection (66.2%) and heavy alcohol consumption (60.6%) were the most frequently identified risk factors for hepatocellular carcinoma. The majority of patients (88.0%) presented late with advanced stages. HBsAg was positive in 66.2% of the patients and Hepatitis C Virus antibody in 16.9%. Thirteen (9.2%) patients tested positive for HIV infection. Most patients (52.8%) had both right and left lobe involvement. The trabecular pattern (47.9%) was the most frequent histopathological type. None of patients had curative therapy because of the advanced nature of the disease. Coagulopathy (45.7%) was the most common complications. The overall mortality rate was 46.5% and it was significantly associated with comorbidity, HIV positivity, CD4+ count <200 cells/μl, high histological grade, advanced stage of the tumor, presence of distant metastases at the time of diagnosis, and associated complications ( P < 0.001). The overall median duration of hospital stay was 14 days. The majority of patients (71.1%) were lost to follow-up at the end of the follow-up period.

          Conclusions

          Hepatocellular carcinoma patients in this region are relatively young at diagnosis and the majority of them present late with an advanced stage and high rate of distant metastasis. Lack of awareness of the disease, poor accessibility to healthcare facilities, and lack of screening programs in this region may contribute to advanced disease at the time of diagnosis. There is a need for early detection, adequate treatment, and proper follow-up to improve treatment outcome.

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          Most cited references15

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          Hepatocellular carcinoma and hepatitis B virus. A prospective study of 22 707 men in Taiwan.

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            Epidemiology and natural history of hepatocellular carcinoma.

            Hepatocellular carcinoma (HCC) is a major contributor to cancer incidence and mortality. There is a wide variation, however, in the global distribution of HCC. Eighty percent of the burden is borne by countries in Asia and sub-Saharan Africa. In most high-risk countries, principal risk factors include infection with hepatitis B virus and dietary exposure to aflatoxin B(1). In contrast, hepatitis C virus and alcohol consumption are more important risk factors in low-risk countries. In recent years, the incidence of HCC has decreased in some high-risk countries and increased in some low-risk countries. Reasons for both trends are not completely understood, but are likely related to public health efforts in Asia and the increase in hepatitis C virus infection in low-risk countries. Vaccination programs against hepatitis B virus will likely decrease the HCC rate even further in decades to come.
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              Role of reproductive factors in hepatocellular carcinoma: Impact on hepatitis B- and C-related risk.

              Hepatocellular carcinoma (HCC) is more prevalent in men than in women. Estrogen may play some role in the development of HCC. We conducted a multicenter case-control study to evaluate the effects of reproductive factors on HCC risk, and to assess whether the association between each factor and HCC differs between hepatitis B surface antigen (HBsAg)-positive and -negative women, in which hepatitis C virus (HCV) is the major cause of HCC. The study included 218 women with HCC and 729 control women selected from nonbiological and first-degree female relatives of patients with HCC. The risk of HCC was inversely related to the number of full-term pregnancies (FTP) (P(trend) =.0216) and age at natural menopause (P(trend) =.0251 among women aged 45-55 without prior surgical menopause). Oophorectomy at age or=16 years), which increased HCC risk in HBsAg carriers (multivariate-adjusted OR, 6.96; 95% CI, 2.52-19.18) but posed no increased risk in noncarriers (P(interaction) =.0053). In conclusion, increased exposure to estrogen during adulthood may provide a protective effect against HCC. Nevertheless, an early menarche, which results in early estrogen exposure, does not confer protection for HBsAg carriers.
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                Author and article information

                Contributors
                Journal
                World J Surg Oncol
                World J Surg Oncol
                World Journal of Surgical Oncology
                BioMed Central
                1477-7819
                2014
                2 August 2014
                : 12
                : 246
                Affiliations
                [1 ]Department of Internal Medicine, Catholic University of Health and Allied Sciences- Bugando, P.O. Box 1464, Mwanza, Tanzania
                [2 ]Department of Microbiology & Immunology, Catholic University of Health and Allied Sciences- Bugando, P.O. Box 1464, Mwanza, Tanzania
                [3 ]Department of Pathology, Catholic University of Health and Allied Sciences- Bugando, Bugando, P.O. Box 1464, Mwanza, Tanzania
                [4 ]Department of Oncology, Catholic University of Health and Allied Sciences- Bugando, Bugando, P.O. Box 1464, Mwanza, Tanzania
                [5 ]Department of Surgery, Catholic University of Health and Allied Sciences- Bugando, Bugando, P.O. Box 1464, Mwanza, Tanzania
                Article
                1477-7819-12-246
                10.1186/1477-7819-12-246
                4121298
                25085449
                bab52657-eb1c-47e7-b39d-8b7a82454acf
                Copyright © 2014 Jaka et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.

                History
                : 9 August 2013
                : 4 July 2014
                Categories
                Research

                Surgery
                hepatocellular carcinoma,clinicopathological,challenges,resource-limited setting,tanzania
                Surgery
                hepatocellular carcinoma, clinicopathological, challenges, resource-limited setting, tanzania

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