Opisthorchiasis from imported raw fish.
Liver fluke infection caused by trematodes belonging to the family Opisthorchiidae--Opisthorchis viverrini, O. felineus, and Clonorchis sinensis--is a major public health problem in many parts of the Far East, Southeast Asia, and eastern Europe. An estimated 17 million persons worldwide are infested: 7 million with C. sinensis, 9 million with O. viverrini, and 1.6 million with O. felineus. O. vivervini is prevalent in Thailand, Lao People's Democratic Republic, and Cambodia; C. sinensis is widespread in Korea, China, Taiwan, and Vietnam; and O. felineus is found in the Russian Federation and eastern Europe. Migration and global tourism are responsible for cases diagnosed in areas where the disease is not endemic (1).
The adult worms are flat, leaf-shaped, transparent, and hermaphroditic flukes that reproduce by self-fertilization. They live in the biliary and pancreatic ducts and occasionally in the gallbladder. The eggs are passed with the feces of the definitive natural host (cats, dogs, pigs, and many other fish-eating mammals) and are mature at excretion. The embryonated eggs are ingested by the intermediate host, a suitable freshwater snail, which varies geographically and according to the parasite species (2). In the digestive tract of the snail, the eggs hatch and become miracidia that go through several developmental stages and multiply asexually into thousands of tailed, tree-swimming cercariae. The cercariae penetrate under the scales of a susceptible fish, which serves as the second intermediate host; they encyst as metacercaria, mainly in the fish body muscles. Fish belonging to the family Ciprinidae (carp) are the major intermediate host of Clonorchis sinensis and Opisthorchis spp. (2). However, a wide range of species of freshwater fish can be naturally infected by liver flukes, and more than one fish species in any aquatic environment can become infected (2). Humans, as incidental definitive hosts, are infected by ingesting a raw fish containing metacercariae. After excysting in the duodenum, the metacercariae migrate through the ampulla of Vater into the bile ducts, where they mature into adult worms within 4 weeks and deposit yellow, operculated eggs. The parasites may live for up to 45 years in a human host, producing 1,000 2,500 eggs per day (2).
The infection is associated with a number of hepatobiliary diseases. The pathologic and clinical consequences of opisthorchiasis are related to the intensity and duration of cumulative infestations. The flukes cause mechanical injury to the bile ducts, and their metabolic products irritate the biliary epithelial cells, leading to cell desquamation, hyperplasia, dysplasia, and eventual fibrosis or cancer. Chronic infestation can result in obstruction of the biliary tract, dilatation of intrahepatic ducts, and subsequent cystic and saccular formations. The gallbladder may enlarge and become nonfunctional, containing muddy bile (3). Because adult flukes are long-lived, they can produce eggs and symptoms long alter the human host has emigrated from the area (4). The acute symptoms of O. felineus infection consist of high-grade fever, malaise, anorexia, diarrhea or constipation, dull pain and discomfort in the upper right quadrant of the abdomen, arthralgia, lymphadenopathy, and urticarial skin rash. Subacute and chronic complications include suppurative cholangitis, liver abscess, and cholangiocarcinoma (2). Acute infestation with C. sinensis is usually asymptomatic, although some patients may have fever, rash, malaise, and abdominal discomfort in the right upper quadrant. Chronic clonorchiasis may be complicated with gallbladder and intrahepatic duct stones, recurrent pyogenic cholangitis, cholecystitis, liver abscess, and cholangiocarcinoma (5). Most persons with O. viverrini infection have no symptoms. Only 5%-10% of heavily infected persons have nonspecific chronic symptoms, such as right upper quadrant abdominal pain, flatulence, and fatigue. Cholangiocarcinoma is a known complication (5).
We report herein on a familial outbreak of liver fluke infection due to eating raw fish personally imported from Siberia. While ample information is available on the biology and epidemiology of liver fluke infection in Southeast Asia (recently summarized in a special issue of Acta Tropica ), reports in the English language literature on the situation in the former Soviet Union are scarce (2). Because so many persons have emigrated from the former USSR to Western countries in recent years, physicians in these countries should be more familiar with the condition; thus, review of the epidemiology of opisthorchiasis in former USSR is appropriate.
Patients and Methods
A 46-year-old woman and her 47-year-old husband, who immigrated from Siberia to Israel 7 years earlier, were admitted because of gastrointestinal complaints of 10 days' duration. The symptoms included nausea, vomiting, yellow sclera, diffuse arthralgia (in the woman), weakness, rigors, and fever up to 39[degrees]C. On admission, the woman was afebrile, and results of her physical examination were normal. The husband's temperature was 38.4[degrees]C; his enlarged, nontender liver was palpated 3 cm below the right costal margin, and his sclera were jaundiced. Laboratory findings in both patients (Table) consisted of marked leukocytosis with notable eosinophilia and elevation of liver enzymes. Ultrasonographic examination of the abdomen showed a slightly enlarged spleen in both patients, and an enlarged liver in the husband.
The triad of abdominal symptoms, eosinophilia, and liver enzyme impairment evoked the possibility of a helminthic infection. On further questioning, the couple recalled having eaten a smoked carp 10 days before becoming sick. The fish was bought in Nizhnevartovsk, Siberia, and was brought to Israel by the couple's son. The other members of the family, the couple's 23-year-old son and 17-year-old daughter, and a friend had also eaten the imported fish. They were asymptomatic at the time of the investigation, although the son reported a short febrile episode that resolved spontaneously, and the daughter had transient abdominal pain in the right upper quadrant. Their leukocyte counts and liver enzyme test results were normal (Table). The wife also recalled having had similar symptoms 15 years earlier, while still living in Siberia. A diagnosis of opisthorchiasis was made on the basis of ova identified in the bile from the wife.
Stool samples from the five persons were examined for ova after concentration with the formaldehyde-ether technique. Opisthorchis/Clonorchis eggs (Figure 1) were found in all stool samples with the exception of that belonging to patient 5, the friend. The fish was not available for examination.
[FIGURE 1 OMMITED]
Treatment consisting of praziquantel, 25 mg/kg orally three times daily for 1 day, was administered to the infected patients (with positive stools for ova). The symptomatic patients (wife and husband) improved promptly, both clinically and as evidenced by laboratory values. On follow-up 2 weeks later, leukocyte count and liver enzyme levels had returned to normal (Table).
The diagnosis of liver fluke infection in this outbreak was confirmed by identifying ova in stool. Determining correctly the species of the causative parasite on the basis of egg form and shape is more challenging because eggs of O. viverrini, O. felineus, and C. sinensis are morphologically similar, and the differentiation is difficult even for experts (3,7). Only the identification of adult worms will confirm the species (3). It has been suggested that O. felineus differ from the other two flukes in the ratio of the length to the width of the egg, which is 1:3 in the former and 1:2 in the latter (3). However, we could not find additional evidence in the literature in support of this statement (4). Although the ova identified in our patients had a ratio of 1:2, we believe that the infection in this outbreak was caused by O. felineus on the basis of the source of the consumed fish and the acute symptoms in two of the four infested family members. In fact, Nizhnevartovsk is located in the Ob River basin, where O. felineus infection is hyperendemic (8). In addition, acute serum sickness like symptoms are much more common after O. felineus infection than after infection with O. viverrini or C. sinensis (4,5). Moreover, O. viverrini is not endemic in the Russian Republic, while C. sinensis is found only in the Amur River area on the Russian-Chinese border (2).
O. Jelineus infection is the most prevalent foodborne liver fluke infection of humans in Russia, Ukraine, and Kazakstan (Figure 2). Infestation usually follows consumption of raw, slightly salted, and frozen fish ("stroganina"). The parasite is endemic in an area that covers nearly all the territory of the Russian Federation with the exception of the northern parts of Siberia and the far-eastern regions. The largest parasite-endemic area is in western Siberia, namely the Ob and Irtysh River valleys and their tributaries (9-12). In the central part of this area, the Tyumen and Tomsk Districts, the mean prevalence of human infection is 40%-95%. Prevalences of 45% to 65% were reported in the Komi-Permiak national district, and infection rates up to 46% have been documented in some communities in Omsk District. Other districts and territories where opisthorchiasis is endemic include the Yekaterinburg (formally Sverdlovsk) District (13), Altai territory, Voronezh District (14), Volga River valley (15) and Archangelsk District in western Russia, and the Angara River (16), Krasnoyarsk territory, and Irkutsk District in eastern Siberia (2). In Ukraine, opisthorchiasis is limited to the Sumy, Poltava, and Chernigov Districts of the Dnieper River basin (17,18), where the prevalence is 5%-40%. In Kazakstan, opistorchiasis is endemic in the Aktyubinsk, Dzhezkazgan, Karaganda, Pavlodar, Tselinograd, and Turgay Districts. Foci of opisthorchiasis have also been found in the Brest, Golnel, and Grodno provinces of Belarus (2). Limited endemic foci of opisthorchiasis in some areas of the Baltic States, eastern Germany, and Poland were described before the Second World War; however, no recent information on the occurrence of the infection in humans in these countries is available.
The correlation between O. felineus infection and cholangiocarcinoma was studied in the Tyumen region, Russia. In the southern part of the region, where 0.5% of the population was infected with O. felineus, the prevalence of cholangiocarcinoma was 4.4 per 100,000 population. In the central area of Tyumen with 45% prevalence of O. felineus infestation, the rate of cholangiocarcinoma was 10-fold higher than in the south (49.8 per 100,000 population) (2).
C. sinensis infection is endemic in the Amur River valleys and Khabarovsk territory, situated in the far eastern part of the Russian Federation. The prevalence of the infection in the native Nanai population is 24% in the most affected villages (2,19).
The major snail hosts for O. Jelineus are Codiella (Bithynia) inflata, C. troscheli, and C. leachi. C. sinensis is transmitted by a wide range of operculate snails, Parafossarulus manchouricus being the main one (2). Twenty-two species of 17 genera of the family Ciprinidae are infected by O. felineus; the most important are Lettciscus idus, L. leuciscus, and Rutilus rutilus; five species host the C. sinensis fluke (2).
The growing volume of international travel and population migration, facilitated by increasing availability of air transportation, is responsible for cases of opisthorchiasis and clonorchiasis diagnosed in non-disease-endemic countries, mainly in North America. Most reports from the United States and Canada describe the detection of Opisthorchis/Clonorchis ova in immigrants from Southeast Asia with chronic infection (20 27). The infection was also documented in North American residents who contracted the disease during long-term or short visits to disease-endemic areas (22). In the United States, liver fluke infection continues to be an active health problem for hundreds of thousands of Southeast Asian refugees who have immigrated since 1975. Clonorchis infestation was documented in 26% of 150 Chinese immigrants in New York City (21). Stool examinations of 186 lndochinese refugees in California have detected C. sinesis eggs in 13% (23). In another report, the prevalence of Opisthorchis eggs among 226 asymptomatic adult Southeast Asian immigrants to the United States was 11% (24). In Montreal, Canada, Clonorchis infestation was documented in 15.5% of 400 Chinese immigrants (20).
We have identified only two reports (in German) of patients of Russian origin whose conditions were diagnosed in western Europe. A 58-year-old woman, who emigrated from Tomsk a year earlier, was seen in Wiesbaden, Germany, for right upper abdominal and flank pain, reduced appetite, and weight loss; O. felineus eggs were detected in stool and duodenal aspirate (28). For two patients from Siberia with suspected eosinophilic leukemia and carcinoma of the gallbladder, respectively, opisthorchiasis was diagnosed in Hamburg (29).
Unlike previous reports of opisthorchiasis diagnosed in non disease-endemic countries, which included patients infected in areas endemic for disease, the patients in the present series were infected outside an endemic region by food imported illegally from a country where the disease was highly prevalent. An estimated 2 million citizens from the former USSR have moved since the Soviet collapse in 1989, mostly to North America, western Europe (mainly Germany), and Israel (30). Most of these immigrants continue to maintain strong cultural ties with their countries of origin, including through eating delicatessen food from the "old country." Thus, both chronic and acute infections can be diagnosed in this population. Physicians providing care to immigrants from the former Soviet Union should be aware of the potential presence of liver fluke infection in these patients and consider the entity in the differential diagnosis, when appropriate.
Dr. Yossepowitch is a fellow in infectious diseases at the E. Wolfson Hospital, Holon, Israel.
Table. Main symptoms and laboratory findings in persons who are raw fish imported from Siberia (a,b) Relationship Time GI symptoms Temp, [degrees]C Wife Pretherapy Vomiting, jaundice 38.4 Posttherapy (c) None 36.0 Follow-up (d) None 36.4 Husband Pretherapy Nausea 39.0 Posttherapy None 36.8 Follow-up None 36.6 Son Pretherapy None 36.5 Posttherapy None ND Follow-up None 36.6 Daughter Pretherapy RUQ pain 36.0 Posttherapy None ND Follow-up None 36.6 Friend On admission None 36.6 WBC Relationship x[10.sup.3]/[micro]L Eosin, % ALT/AST, U/L Wife 58.3 78 125/96 19.2 50 44/29 7.2 6.2 45/37 Husband 16.9 50 188/164 13.4 45.6 170/65 6.85 4.5 48/35 Son 8.2 5.7 28/31 ND ND. ND ND ND ND Daughter 7.23 4.7 33/32 ND ND ND ND ND ND Friend 8.08 1 15/14 ALP, LDH, Bili, Relationship U/L U/L mg/dL Wife 294 528 1.69 178 355 1.09 64.6 ND 0.7 Husband 1147 531 3.17 555 512 1.9 134 390 1.17 Son 110 368 0.77 ND ND ND ND ND ND Daughter 53 377 0.49 ND ND ND ND ND ND Friend 111 372 0.64 (a) GI, gastronintestinal; Temp., temperature, WBC, leukocyte count; eosin, eosinophils; ALT/AST, alanine aminotransterase/aspartate aminotransterase; ALP, alkaline phosphatase; LDH, lactate dehydrogenase; ND, not done; RUQ, right upper quadrant. (b) Abnormal laboratory results are underlined. Normal values: WBC (leukocyte) count, 4-10 x [10.sup.3]/[micro]L; eosinophils, 1%-6%; ALT, 0-41 U/L; AST, 0-38 U/L; ALP, 39-117 U/L; LDH, 240-480; bilirubin, 0.3-1.0 mg/dL. (c) Posttherapy, 4 days after therapy. (d) Follow-up, 2 weeks after therapy.
(1.) Sithithaworn P, Haswell-Elkins M. Epidemiology of Opisthorchis viverrini. Acta Trop. 2003;88:187-94.
(2.) World Health Organization Study Group. Control of foodborne Trematode infections. WHO Technical Report Series 849. Geneva: The Organization; 1995.
(3.) Harinasuta T, Bunnag D. Liver, lung, and intestinal trematodiasis. In: Warren KS, Mahmoud AAF, editors. Tropical and geographical medicine. 2nd ed. New York: McGraw-Hill; 1990. p. 473-89.
(4.) Liu LX, Harinasuta KT. Liver and intestinal flukes. Gastroenterol Clin North Am. 1996;25:627-36.
(5.) Mairianga E, Mairiang R Clinical manifestation of opisthorchiasis and treatment. Acta Trop. 2003;88:221-7.
(6.) Sripa B, Sithithawom P, Sirisinha S. Opisthorchis viverrini and opisthorchiasis: the 21st century review. Acta Trop. 2003;88:169-70.
(7.) Kaewkes S. Taxonomy and biology of liver flukes. Acta Trop. 2003;88:177-86.
(8.) Guzeeva TM, Kliuchnikov SI. Opisthorchiasis morbidity in the town of Nizbnevartovsk (in Russian). Med Parazitol (Mosk). 2002;2:13-5.
(9.) Filatov VG, Pustovalova VIa, Ushakov AV, Maier VA. The role of various intermediate and definitive host species in the dissemination of Opisthorchis felineus from the Ob-Irtysh locus of opisthorchiasis (in Russian). Med Parazitol (Mosk). 1989;3:39-41.
(10.) Zelia OP, Zavoikin VD, Sergeeva MN. The characteristics of the circulation of the causative agent of opisthorchiasis in the tributaries of the Ob (in Russian). Med Parazitol. (Mosk). 1990;4:22-5.
(11.) Fedorov KP, Babueva RV, Karpenko SV. The role of the owsianka Leucaspius delineatus in maintaining opisthorchiasis foci in Novosibirsk Province (in Russian). Med Parazitol (Mosk). 1989;6:64-7.
(12.) Skarednov NI, Ozhirel'ev VV, Maier VA, Serednitskii SI, Satin VA. Ecologo-epidemiologic reasons for the prevalence of opisthorchiasis in the Kurgan region (in Russian). Med Parazitol (Mosk). 1986;6:11-4.
(13.) Tsybina TN. The ecological-epidemiological characteristics of opisthorchiasis in Sverdlovsk Province (in Russian). Med Parazitol (Mosk). 1994;3:45-50.
(14.) Chubirko MI, Sharinova LF, Popova TI, Morozova NN, Starostina LS. The spread of Opisthorchis invasion in Voronezh Proxince (in Russian). Med Parazitol (Mosk). 1997;3:16-9.
(15.) Khamidullin RI, Fomina OA, Sultanaeva EG, Khamidullm IR. Opisthorchiasis and pseudamphistomiasis on the territory of the middle Volga valley (in Russian). Med Parazitol (Mosk). 1995;1:40-2.
(16.) Zelia OP, Gerasimov IV. The possibility of the formation of an opisthorchiasis focus in the lower reaches of the Angara (in Russian). Med Parazitol (Mosk). 1992;1:59.
(17.) Zavoikin VD, Beer SA, Pliushcheva GL, Sholokhova SE. Nikilforova TF. Opisthorchiasis at left Dnieper watersheds (in Russian). Med Parazitol (Mosk). 1989;2:9-14.
(18.) Nesterenko NP, Morozova IA, Kondrat'eva LP, Donets NP. Opisthorchiasis in Chernigov Province (the situation and control and prevention measures) (in Russian). Med Parazitol (Mosk). 1990;4:21-2.
(19.) Figurnov VA, Chertov AD, Romanenko NA, Grigorenko AA, Gavrilow VA, Soldatkin PK, et al. Clonorchiasis in the upper Amur region: biology, epidemiology, clinical presentation (in Russian). Med Parazitol (Mosk). 2002;4:20-3.
(20.) Seah SKK. Intestinal parasites in Chinese immigrants in a Canadian City. J Trop Med Hyg. 1973;76:291-3.
(21.) Kammerer WS, Van der Decker JD, Keith TB, Molt KE. Clonorchiasis in New York City Chinese. Trop Doct. 1977;7:105-6.
(22.) Sun T. Clonorchiasis: a report of four cases and discussion of unusual manifestations. Am J Trop Med Hyg. 1980:29:1223-7.
(23.) Arfaa F. Intestinal parasites among Indochinese refugees and Mexican immigrants resettled in Contra Costa County, California. J Fam Pract. 1981;12:223-6.
(24.) Lerman D, Barrett-Connor E, Norcross W. Intestinal parasites in asymptomatic adult Southeast Asian immigrants. J Fam Pract. 1982:15:443-6.
(25.) Dao AH, Gregory DW, McKee LC. Specific health problems of Southeast Asian refugees in middle Tennessee. South Med J. 1984:77:995-8.
(26.) Schwartz DA. Cholangiocarcinoma associated with liver fluke infection: a preventable source of morbidity in Asian immigrants. Am J Gastroenterol. 1986:81:76-9.
(27.) Dao AH, Barnwell SF, Adkins RB. A case of opisthorchiasis diagnosed by cholangiography and bile examination. Am Surg. 1991:57:206-9.
(28.) Cherdron A, Fiegel P. Opisthorchis felineus--the cat liver fluke. Differential diagnosis of right-side upper abdominal pain (in German). Dtsch Med Wochenschr. 1992;117:328-31.
(29.) Berger B, Vierbuchen M. Opisthorchiasis simulating a malignancy (in German). Z Gastroenterol. 2001;39:173-5.
(30.) Heleniak T. Migration dilemmas haunt post-Soviet Russia. [cited Oct 2002]. Available from http://www.migrationinformation.org
Orit Yossepowitch, * Tamar Gotesman, * Mark Assous, ([dagger]) Esther Manta, ([dagger]) Reuven Zimlichman, * and Michael Dan *
* E. Wolfson Hospital, Holon, Israel; and ([dagger]) Ministry of Health, Jerusalem, Israel
Address for correspondence: Michael Dan, infectious Diseases Unit, E. Wolfson Hospital, Holon 58100, Israel; fax: 972-3-5016126; email: email@example.com
|Printer friendly Cite/link Email Feedback|
|Publication:||Emerging Infectious Diseases|
|Date:||Dec 1, 2004|
|Previous Article:||Venezuelan equine encephalitis virus, southern Mexico.|
|Next Article:||Identifying rodent hantavirus reservoirs, Brazil.|