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Cholangiocarcinoma Secondary to Primary Sclerosing Cholangitis in Explanted Livers: A Single-Center Study in the South of Iran

AUTHORS

Bita Geramizadeh 1 , 2 , * , Roshanak Ghavvas 2 , Kurosh Kazemi 3 , Alireza Shamsaeefar 3 , Saman Nikeghbalian 3 , Seyed-Ali Malekhosseini 3

AUTHORS INFORMATION

1 Department of Pathology, Shiraz University of Medical Sciences, Shiraz, IR Iran

2 Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, IR Iran

3 Department of Hepatobiliary and Liver Transplant Surgery, Shiraz University of Medical Sciences, Shiraz, IR Iran

How to Cite: Geramizadeh B, Ghavvas R, Kazemi K, Shamsaeefar A, Nikeghbalian S, et al. Cholangiocarcinoma Secondary to Primary Sclerosing Cholangitis in Explanted Livers: A Single-Center Study in the South of Iran, Hepat Mon. 2015 ; 15(12):e33626. doi: 10.5812/hepatmon.33626.

ARTICLE INFORMATION

Hepatitis Monthly: 15 (12); e33626
Published Online: December 27, 2015
Article Type: Brief Report
Received: October 6, 2015
Revised: November 24, 2015
Accepted: November 28, 2015
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Abstract

Background: Primary sclerosing cholangitis (PSC) is a chronic disease, characterized by chronic inflammation and fibrosis of bile duct epithelial cells. This is a significant contributory factor to the development of malignancy, most commonly cholangiocarcinoma (CCA), which is the second most common malignant liver tumor.

Objectives: For the first time in Iran, we intend to describe our experience with cases of PSC, with and without CCA, in explanted livers, and compare our results with those found in other areas of the world.

Patients and Methods: The study population comprised 181 individuals with a diagnosis of PSC who had undergone liver transplantation in the main liver transplant center of Iran, the largest center of hepatobiliary surgery in the south of that country, over a 3-year period between 2012 and 2014. All explanted livers, with and without CCA, were evaluated.

Results: Of the 181 patients, 16 were found to have CCA, two of whom had been diagnosed after pathologic study of the explanted livers. Therefore it appeared that 8.8% of the patients with PSC in our center had developed CCA before liver transplantation.

Conclusions: A comparison of our results with those obtained from other centers in both Western and Asian countries (which reported CCA in 3.6% - 36.5% of patients with PSC), shows that the incidence of CCA in the patients we studied is intermediate.

Keywords

Primary Sclerosing Cholangitis Cholangiocarcinoma Liver Transplantation Cirrhosis

Copyright © 2015, Kowsar Corp. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

1. Background

Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease. It is characterized by progressive inflammation and fibrosis of the intra and extrahepatic bile ducts, which leads to progressive cholestasis, hepatic injury, and eventually liver cirrhosis (1). People with PSC are at high risk of developing cholangiocarcinoma (CCA), the reported incidence of which varies across different areas of the world (2). As there is no effective medical treatment for PSC, and liver transplantation (LT) results have been excellent, LT remains the optimum treatment choice for PSC patients with end-stage liver disease (3, 4).

2. Objectives

In this brief report, we describe our experience evaluating the incidence of CCA in people with PSC who have undergone LT. Their explanted livers were studied over a 3 year period in the largest liver transplant center in Iran, and the results were compared to the incidence of CCA secondary to PSC that has been found in different areas of the world. To the best of our knowledge, such a study has not previously been performed in Iran.

3. Patients and Methods

The cases of 181 people with a diagnosis of PSC or CCA who had undergone LT in the liver transplant unit of Namazi Hospital, Shiraz, Iran, between 2012 and 2014 were extracted from the pathology file and evaluated. Those patients with a histopathologically confirmed diagnosis of PSC and CCA were also identified.

4. Results

During the 3-year study period, of the 181 cases of PSC, 16 were found to have CCA and 165 were found to be free of malignancy, following a thorough examination of the explanted livers (Figure 1). Two of the 16 CCA cases were of very small CCA (< 0.5 cm in diameter), in which LT had been performed without a pre-transplant diagnosis of CCA; the diagnosis was made after pathologic examination of the explanted liver (Figure 2). In the remaining 14 CCA cases, this malignancy had been diagnosed pre-transplant (Figure 3). Table 1 shows the characteristics and demographic findings of the PSC patients with and without CCA.

A Section From an Explanted Liver With Primary Sclerosing Cholangitis
Figure 1. A Section From an Explanted Liver With Primary Sclerosing Cholangitis
A Section From an Explanted Liver With Primary Sclerosing Cholangitis and Cholangiocarcinoma (arrow) Diagnosed After Liver Transplantation
Figure 2. A Section From an Explanted Liver With Primary Sclerosing Cholangitis and Cholangiocarcinoma (arrow) Diagnosed After Liver Transplantation
A Section From an Explanted Liver With Primary Sclerosing Cholangitis and Cholangiocarcinoma (arrow) Diagnosed Before Liver Transplantation
Figure 3. A Section From an Explanted Liver With Primary Sclerosing Cholangitis and Cholangiocarcinoma (arrow) Diagnosed Before Liver Transplantation
Table 1. The Characteristics and Demographic Findings of the Individuals With Primary Sclerosing Cholangitis, With and Without Cholangiocarcinoma
NumberaAgebF/M
PSC without CCA165 (91.2)35.98 ± 12.41/1.5
PSC with CCA16 (8.8)48.8 ± 9.21/3

aData are presented as No. (%)

bData are presented as mean±SD.

5. Discussion

PSC is a chronic cholestatic disease, characterized by inflammation and fibrosis of bile ducts, which leads to biliary strictures, stasis, and liver cirrhosis. The worst complication of PSC is the development of CCA, for which there is no effective non-surgical therapy, and which is considered to be a malignancy with a poor prognosis (5). The mean age of our PSC patients who did not have CCA was 35.18 ± 11.7, which was significantly lower than the mean age for patients with concomitant PSC and CCA. It has been reported that development of CCA in patients with PSC usually occurs when these individuals are aged in their 40s. CCA without PSC develops later in life, when people are aged in their 70s (6). In the largest study conducted in Iran, in which 283 people with CCA were followed-up between 2001 and 2004, the mean age of the patients was 59.7 ± 14.4 (2). In our study, the male to female ratio in the 16 CCA patients was 1.3. Mohammad-Alizadeh et al. estimated that this ratio was 1.7 (180 males and 103 females) in 283 Iranian CCA patients (4). Therefore, in people from Iran, CCA is more common in males, which is partly because PSC (the major risk factor for CCA) affects men more than women (7). As has been mentioned, the prevalence of CCA in PSC patients in our center was 8.8 %, with 16 patients of the total number of 181 having concomitant PSC and CCA. It is worth noting that two patients (12.5%) were diagnosed as having CCA only following pathologic study of the explanted liver. The incidence rate of CCA in PSC patients in our center was largely similar to that found in a Swedish study, in which, of 45 cases of PSC, four (8.9%) developed CCA during a 10-year follow-up between1975 and 1984 (8). The lowest prevalence has been reported in Norway (9), with four CCA patients out of 75 PSC cases (5.3%), and the highest prevalence has been reported in Australia, where CCA was diagnosed in four patients out of 11 with PSC at the time of transplantation, and recurrence of tumor was observed in two patients (10).

Among studies from Europe, The Netherlands (5), Germany (11), and Italy (12) have reported a 10.3 %, 12%, and 6% incidence risk, respectively, of CCA in people with PSC. Studies from several US states, showed different association risks and reported prevalence rates of between 7 and 11% (13-18). Studies from Asia reported a lower prevalence rate of CCA in PSC, with 3.6% shown in a Japanese study (7), and 5.3% found in Turkey (19). Table 2 shows the percentage of people with PSC who developed CCA during the years of follow-up or at the time of liver transplantation. In some studies, significant recurrence during follow-up was reported, even after liver transplantation (11).

Table 2. The Incidence of Cholangiocarcinoma in Different Parts of the World in Comparison to Our Center
AuthorCountryIncidence of CCA in PSC Patientsa
Ponsioen et al.(5)The Netherlands10.3
Tanaka et al. (7)Japan3.65
Broome et al.(8)Sweden8.9
Schrumpf et al.(9)Norway5.3
Strasser et al.(10)Australia36.5
Lutz et al.(11)Germany12
Mosconi et al.(12)Italy6
Multiple studies (13-18)USA7-11
Ataseven et al.(19)Turkey5.3
The current studyIran8.8

aData are presented as No. (%)

The incidence rate of CCA secondary to PSC in Namazi Hospital of Shiraz, the largest referral center in the south of Iran, was estimated to be 8.8%, which is intermediate in comparison with other Western and Asian countries. Although we cannot explain the reason for this difference, it appears to be an ethnic and genetic issue. Further prospective studies are necessary to identify the reasons for this difference in incidence.

Acknowledgements

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