Flukes (Liver, Lung, and Intestinal)


Several different trematodes , or flukes, can parasitize humans and cause disease. Flukes are endemic worldwide but are more prevalent in the less developed parts of the world. They include Schistosoma, or the blood flukes (see Chapter 326 ), as well as fluke species that cause infection in the human biliary tree, lung tissue, and intestinal tract. These latter trematodes are characterized by complex life cycles ( Fig. 327.1 ). Sexual reproduction of adult worms in the definitive host produces eggs that are passed in the stool. Larvae, called miracidia , develop in freshwater. These in turn infect certain species of mollusks (aquatic snails or clams), in which asexual multiplication by parasite larvae produces cercariae. Cercariae then seek a 2nd intermediate host, such as an insect, crustacean, or fish, or attach to vegetation to produce infectious metacercariae . Humans acquire liver, lung, and intestinal fluke infections by eating uncooked, lightly cooked, pickled, or smoked foods containing these infectious parasite cysts. The “alternation of generations” requires that flukes parasitize more than 1 host (often 3) to complete their life cycle. Because parasitic flukes are dependent on these nonhuman species for transmission, the distribution of human fluke infection closely matches the ecologic range of the flukes’ intermediate hosts. As a group, these parasites are commonly referred to as food-borne trematodes .

Fig. 327.1
Life cycle of parasitic liver, lung, and intestinal flukes.
C.s., Clonorchis sinensis ; F.b., Fasciolopsis buski ; F.h., Fasciola hepatica ; P.w., Paragonimus westermani.

(Adapted from Mandell GL, Bennett JE, Dolin R, editors: Principles and practice of infectious diseases , ed 7, Philadelphia, 2010, Elsevier, Fig 289-2.)

Liver Flukes

Fascioliasis (Fasciola hepatica)

Fasciola hepatica, the sheep liver fluke, infects cattle, other ungulates, and occasionally humans. This infection affects approximately 17 million people worldwide and has been reported in many different parts of the world, particularly South America, Europe, Africa, China, Australia, and Cuba. Although F. hepatica is enzootic in North America, reported cases are extremely rare. Humans are infected by ingestion of metacercariae attached to vegetation, especially wild watercress, lettuce, and alfalfa. In the duodenum, the parasites excyst and penetrate the intestinal wall, liver capsule, and parenchyma. They wander for a few weeks before entering the bile ducts, where they mature. Adult F. hepatica (1-2.5 cm) commence oviposition approximately 12 wk after infection; the eggs are large (75-140 µm) and operculated. They pass to the intestines with bile and exit the body in the feces (see Fig. 327.1 ). On reaching freshwater, the eggs mature and hatch into miracidia, which infect specific snail intermediate hosts to multiply into many cercariae. These then emerge from infected snails and encyst on aquatic grasses and plants.

Clinical manifestations usually occur either during the liver migratory phase of the parasites or after their arrival at their final habitat in upper bile ducts. Fever, right upper quadrant pain, and hepatosplenomegaly characterize the 1st phase of illness. Peripheral blood eosinophilia is usually marked. As the worms enter bile ducts, most of the acute symptoms subside. On rare occasions, patients may have obstructive jaundice or biliary cirrhosis, with signs of cholestasis, ascending cholangitis, cholelithiasis and jaundice and increased liver enzymes, direct bilirubin, and γ-glutamyl transpeptidase. F. hepatica infection is diagnosed by identifying the characteristic eggs in fecal smears or duodenal aspirates. Diagnosis can be suggested by positive serology and imaging that reveals acute, hypodense liver lesions that change over time. Presentation can be dramatic in children, with features including generalized edema, hepatic cirrhosis with esophageal varices, and in severe cases, death from generalized organ failure.

The recommended treatment of fascioliasis is triclabendazole (10 mg/kg orally [PO] once or twice) or bithionol (30-50 mg/kg PO once daily on alternate days for a total of 10-15 doses). In the United States, bithionol is not generally available, but may be available from compounding pharmacies.

You're Reading a Preview

Become a Clinical Tree membership for Full access and enjoy Unlimited articles

Become membership

If you are a member. Log in here