Consult the medical resource doctors trust

UpToDate is one of the most respected medical information resources in the world, used by over 360,000 doctors and thousands of patients to find answers to medical questions.

  • Content written by a faculty of over 4,000 physicians from leading medical institutions
  • Unbiased: free of advertising or pharmaceutical funding
  • Evidence-based treatment recommendations
  • Continuously updated to incorporate new medical findings

Related articles included with a subscription

Liver flukes: Clonorchiasis and opisthorchiasis

INTRODUCTION

The three major liver trematodes or flukes that infect humans are Clonorchis sinensis, Opisthorchis species, and Fasciola hepatica. Clonorchiasis, opisthorchiasis, and the North American liver fluke, Metorchis conjunctus, will be reviewed here. Fascioliasis is discussed separately. (See "Liver flukes: Fascioliasis".)

CLONORCHIS SINENSIS AND OPISTHORCHIS SPECIES

C. sinensis and Opisthorchis species are parasite flatworms. They are leaf-shaped and hermaphroditic, ranging in size from a few millimeters to several centimeters. The adult flukes allow differentiation of species, although the eggs of these parasites are all yellowish-brown in color, oval in shape, and measure approximately 20 to 30 µm by 15 µm, making species identification difficult. The eggs also resemble those of other intestinal flukes.

The adult flukes undergo asexual reproduction in snails, which are the intermediate host, and undergo sexual reproduction in definitive mammalian hosts. Humans are accidental hosts. Different genera of snails and different species of fish serve as the first and second intermediate hosts respectively for the different flukes. The geographical ranges and habitats of these fish and snail species contribute to the geographic distributions of human infection by each of these flukes. Distribution is also determined by local eating habits.

Epidemiology — C. sinensis, also known as the Chinese liver fluke, is endemic in the Far East, particularly in China, Japan, Taiwan, Vietnam and Korea [1,2]. It is a parasite of fish-eating mammals, with dogs and cats the most common reservoirs. The adult worms are flat and elongated, measuring 10 to 25 mm long and 3 to 5 mm wide. It is estimated that more than 7 million people are infected worldwide. Prevalence rates in endemic areas vary widely. As an example, prevalence rates in different provinces of China range from <1 to 57 percent [3]. One study in Korea showed a prevalence of 16 percent [4].

The two species that most frequently cause human opisthorchiasis are O. felineus and O. viverrini. They are common liver flukes of cats, dogs and other fish-eating mammals, which serve as reservoir hosts. O. felineus occurs in Southeast Asia and in Central and Eastern Europe, particularly in Siberia and other parts of the former Soviet Union. Prevalence rates of 40 to 95 percent in some areas, and infection of over 16 million people is estimated [5]. O. viverrini is endemic in Thailand, Kampuchea and Laos. Prevalence rates of over 24 to 90 percent in villages in Thailand and 40 to 80 percent in Laos have been reported, and it is estimated that over 10 million people are infected [5-7]. Both O. felineus and O. viverrini are usually 8 to 12 mm long, but O. felineus tends to be wider (2 to 3 mm compared to 1 to 2 mm).

To continue reading this article you need to subscribe.

Read the rest of this article and others like it

The content on the UpToDate website is not intended nor recommended as a substitute for medical advice, diagnosis, or treatment. Always seek the advice of your own physician or other qualified health care professional regarding any medical questions or conditions. The use of this website is governed by the UpToDate Terms of Use (click here) ©2009 UpToDate, Inc.
References Top
  1. Rim, HJ. Clonorchiasis: an update. J Helminthol 2005; 79:269.
  2. Wang, KX, Zhang, RB, Cui, YB, et al. Clinical and epidemiological features of patients with clonorchiasis. World J Gastroenterol 2004; 10:446.
  3. Maclean, JD, Cross, J, Mahanty, S. Liver, lung, and intestinal fluke infections. In: Tropical Infectious Diseases: Principles, Pathogens and Practice. 2nd ed. Guerrant, RL, Waker, DH, Weller, PF (Eds), Churchill Livingstone, Philadelphia 2006. p. 1349.
  4. Kim, BJ, Ock, MS, Kim, IS, Yeo, UB. Infection status of Clonorchis sinensis in residents of Hamyang-gun, Gyeongsangnam-do, Korea. Korean J Parasitol 2002; 40:191.
  5. Control of foodborne trematode infections. Report of a WHO Study Group. World Health Organ Tech Rep Ser 1995; 849:1.
  6. Ramasoota, T. Current status of food-borne parasitic zoonoses in Thailand. Southeast Asian J Trop Med Public Health 1991; 22 Suppl:23.
  7. Harinasuta, T, Pungpak, S, Keystone, JS. Trematode infections. Opisthorchiasis, clonorchiasis, fascioliasis, and paragonimiasis [published erratum appears in Infect Dis Clin North Am 1994 Mar; 8(1):following table of contents]. Infect Dis Clin North Am 1993; 7:699.
  8. Liu, LX, Harinasuta, KT. Liver and intestinal flukes. Gastroenterol Clin North Am 1996; 25:627.
  9. Schwartz, DA. Cholangiocarcinoma associated with liver fluke infection: a preventable source of morbidity in Asian immigrants. Am J Gastroenterol 1986; 81:76.
  10. Lewin, MR, Weinert, MF. An eighty-four-year-old man with fever and painless jaundice: a case report and brief review of Clonorchis sinensis infection. J Travel Med 1999; 6:207.
  11. Chan, CW, Lam, SK. Diseases caused by liver flukes and cholangiocarcinoma. Baillieres Clin Gastroenterol 1987; 1:297.
  12. Sithithaworn, P, Haswell-Elkins, MR, Mairiang, P, et al. Parasite-associated morbidity: liver fluke infection and bile duct cancer in northeast Thailand. Int J Parasitol 1994; 24:833.
  13. Upatham, ES, Viyanant, V, Kurathong, S, et al. Relationship between prevalence and intensity of Opisthorchis viverrini infection, and clinical symptoms and signs in a rural community in north-east Thailand. Bull World Health Organ 1984; 62:451.
  14. Upatham, ES, Viyanant, V, Kurathong, S, et al. Morbidity in relation to intensity of infection in Opisthorchiasis viverrini: study of a community in Khon Kaen, Thailand. Am J Trop Med Hyg 1982; 31:1156.
  15. Mairiang, E, Haswell-Elkins, MR, Mairiang, P, et al. Reversal of biliary tract abnormalities associated with Opisthorchis viverrini infection following praziquantel treatment. Trans R Soc Trop Med Hyg 1993; 87:194.
  16. Pungpak, S, Harinasuta, T, Bunnag, D, et al. Fecal egg output in relation to worm burden and clinical features in human opisthorchiasis. Southeast Asian J Trop Med Public Health 1990; 21:275.
  17. Pungpak, S, Chalermrut, K, Harinasuta, T, et al. Opisthorchis viverrini infection in Thailand: symptoms and signs of infection--a population-based study. Trans R Soc Trop Med Hyg 1994; 88:561.
  18. Watanapa, P, Watanapa, WB. Liver fluke-associated cholangiocarcinoma. Br J Surg 2002; 89:962.
  19. Okuda, K, Kubo, Y, Okazaki, N, et al. Clinical aspects of intrahepatic bile duct carcinoma including hilar carcinoma: a study of 57 autopsy-proven cases. Cancer 1977; 39:232.
  20. Pungpak, S, Radomyos, P, Radomyos, BE, et al. Treatment of Opisthorchis viverrini and intestinal fluke infections with Praziquantel. Southeast Asian J Trop Med Public Health 1998; 29:246.
  21. Sakolvaree, Y, Ybanez, L, Chaicumpa, W. Parasites elicited cross-reacting antibodies to Opisthorchis viverrini. Asian Pac J Allergy Immunol 1997; 15:115.
  22. Akai, PS, Pungpak, S, Chaicumpa, W, et al. Serum antibody responses in opisthorchiasis. Int J Parasitol 1995; 25:971.
  23. Sirisinha, S, Chawengkirttikul, R, Haswell-Elkins, MR, et al. Evaluation of a monoclonal antibody-based enzyme linked immunosorbent assay for the diagnosis of Opisthorchis viverrini infection in an endemic area. Am J Trop Med Hyg 1995; 52:521.
  24. Wongsaroj, T, Sakolvaree, Y, Chaicumpa, W, et al. Affinity purified oval antigen for diagnosis of Opisthorchiasis viverrini. Asian Pac J Allergy Immunol 2001; 19:245.
  25. Lin, YL, Chen, ER, Yen, CM. Antibodies in serum of patients with clonorchiasis before and after treatment. Southeast Asian J Trop Med Public Health 1995; 26:114.
  26. Kim, SI. A Clonorchis sinensis-specific antigen that detects active human clonorchiasis. Korean J Parasitol 1998; 36:37.
  27. Wongratanacheewin, S, Pumidonming, W, Sermswan, RW, et al. Detection of Opisthorchis viverrini in human stool specimens by PCR. J Clin Microbiol 2002; 40:3879.
  28. Elkins, DB, Mairiang, E, Sithithaworn, P, et al. Cross-sectional patterns of hepatobiliary abnormalities and possible precursor conditions of cholangiocarcinoma associated with Opisthorchis viverrini infection in humans. Am J Trop Med Hyg 1996; 55:295.
  29. Hong, ST, Yoon, K, Lee, M, et al. Control of clonorchiasis by repeated praziquantel treatment and low diagnostic efficacy of sonography. Korean J Parasitol 1998; 36:249.
  30. Choi, D, Hong, ST, Lim, JH, et al. Sonographic findings of active clonorchis sinensis infection. J Clin Ultrasound 2004; 32:17.
  31. Lim, JH. Radiologic findings of clonorchiasis. AJR Am J Roentgenol 1990; 155:1001.
  32. Jeong, YY, Kang, HK, Kim, JW, et al. MR imaging findings of clonorchiasis. Korean J Radiol 2004; 5:25.
  33. Drugs for Parasitic Infections. Medical Let Drugs Ther 2004. (www.medicalletter.org).
  34. Jong, EC, Wasserheit, JN, Johnson, RJ, et al. Praziquantel for the treatment of Clonorchis/Opisthorchis infections: report of a double-blind, placebo-controlled trial. J Infect Dis 1985; 152:637.
  35. Tinga, N, De, N, Vien, HV, et al. Little effect of praziquantel or artemisinin on clonorchiasis in Northern Vietnam. A pilot study. Trop Med Int Health 1999; 4:814.
  36. Bunnag, D, Harinasuta, T. Studies on the chemotherapy of human opisthorchiasis: III. Minimum effective dose of praziquantel. Southeast Asian J Trop Med Public Health 1981; 12:413.
  37. Pungpak, S, Bunnag, D, Harinasuta, T. Clinical and laboratory evaluation of praziquantel in opisthorchiasis. Southeast Asian J Trop Med Public Health 1983; 14:363.
  38. Pungpark, S, Bunnag, D, Harinasuta, T. Albendazole in the treatment of opisthorchiasis and concomitant intestinal helminthic infections. Southeast Asian J Trop Med Public Health 1984; 15:44.
  39. Liu, YH, Wang, XG, Gao, P, Qian, MX. Experimental and clinical trial of albendazole in the treatment of Clonorchiasis sinensis. Chin Med J (Engl) 1991; 104:27.
  40. Jaroonvesama, N, Charoenlarp, K, Cross, JH. Treatment of Opisthorchis viverrini with mebendazole. Southeast Asian J Trop Med Public Health 1981; 12:595.
  41. Viravan, C, Bunnag, D, Harinasuta, T, et al. Clinical field trial of praziquantel in opisthorchiasis in Nong Rangya Village, Khon Kaen Province, Thailand. Southeast Asian J Trop Med Public Health 1986; 17:63.
  42. Vivatanasesth, P, Sornmani, S, Schelp, FP, et al. Mass treatment of opisthorchiasis in Northeast Thailand. Southeast Asian J Trop Med Public Health 1982; 13:609.
  43. Jongsuksuntigul, P, Imsomboon, T. Epidemiology of opisthorchiasis and national control program in Thailand. Southeast Asian J Trop Med Public Health 1998; 29:327.
  44. Jongsuksuntigul, P, Imsomboon, T. The impact of a decade long opisthorchiasis control program in northeastern Thailand. Southeast Asian J Trop Med Public Health 1997; 28:551.
  45. Brassard, P, Hoey, J, Ismail, J, Gosselin, F. The prevalence of intestinal parasites and enteropathogenic bacteria in James Bay Cree Indians, Quebec. Can J Public Health 1985; 76:322.
  46. Behr, MA, Gyorkos, TW, Kokoskin, E, et al. North American liver fluke (Metorchis conjunctus) in a Canadian aboriginal population: a submerging human pathogen?. Can J Public Health 1998; 89:258.
  47. MacLean, JD, Arthur, JR, Ward, BJ, et al. Common-source outbreak of acute infection due to the North American liver fluke Metorchis conjunctus. Lancet 1996; 347:154.
white circle LOG IN
white circle DEMO