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Occup Environ Med doi:10.1136/oemed-2012-101246
  • Workplace
  • Short report

Cholangiocarcinoma among offset colour proof-printing workers exposed to 1,2-dichloropropane and/or dichloromethane

  1. Gaku Ichihara4
  1. 1Department of Occupational and Environmental Management, University of Occupational and Environmental Health, Kitakyusyu, Japan
  2. 2Department of Community Health and Epidemiology, Nara Medical University School of Medicine, Kashihara, Japan
  3. 3Department of Hepato-Biliary-Pancreatic Surgery, Osaka Red Cross Hospital, Osaka, Japan
  4. 4Department of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan
  1. Correspondence to Dr Shinji Kumagai, Department of Occupational and Environmental Management, University of Occupational and Environmental Health, 1-1, Iseigaoka, Yawata-nishi-ku, Kitakyusyu 807-8555, Japan; shkumagai{at}health.uoeh-u.ac.jp
  • Received 21 October 2012
  • Revised 24 February 2013
  • Accepted 26 February 2013
  • Published Online First 14 March 2013

Abstract

Objectives The present study was conducted to investigate the relationship between occupational chemical exposure and incidence of cholangiocarcinoma among workers in the offset colour proof-printing section of a small printing company in Osaka, Japan.

Methods We identified 51 men who had worked in the proof-printing room, and 11 men who had worked in the front room for at least 1 year between 1991 and 2006. We interviewed them about the chemicals they used, and estimated their levels of exposure to chemicals. We also investigated the medical records of 11 cholangiocarcinoma patients, and calculated the standardised mortality ratio (SMR) from 1991 to 2011.

Results Workers used 1,2-dichloropropane (1,2-DCP) from approximately 1985 to 2006, and dichloromethane (DCM) from approximately 1985 to 1997/1998. Exposure concentrations were estimated to be 100–670 ppm for 1,2-DCP and 80–540 ppm for DCM among the proof-printing workers. All 11 patients were pathologically diagnosed with cholangiocarcinoma. Ages at diagnosis were 25–45 years, and ages at death were 27–46 years among the six deceased individuals. The primary cancer site was the intrahepatic bile duct for five patients, and the extrahepatic bile ducts for six. All patients were exposed to 1,2-DCP for 7–17 years and diagnosed with cholangiocarcinoma 7–20 years after their first exposure. Ten patients were also exposed to DCM for 1–13 years. The SMR for cholangiocarcinoma was 2900 (expected deaths: 0.00204, 95% CI 1100 to 6400) for all workers combined.

Conclusions These findings suggest that 1,2-DCP and/or DCM may cause cholangiocarcinoma in humans.

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