Case Report
Human Fascioliasis: Diagnosis by Typical Computed Tomography Features and Response to Nitazoxanide in 16 Patients from India
Rochita Venkata Ramanan1, Ubal Dhus2, Anand Ramamurthy3, Sarojini Ashok Parameswaran2, Paramasivan Piramanayagam3, Ram Gopalakrishnan4
1Department of Radiology, 2Department of Medical Gastroenterology, 3Department of Liver transplantation and Hepatobiliary surgery, 4Institute of Infectious Diseases, Apollo Hospital, Chennai, India

Corresponding Author
Dr Rochita Venkata Ramanan


Fascioliasisis a food-borne hepatic trematode zoonosis caused by the liver fluke Fasciola hepatica (FH). Though common in developing countries and not uncommon in Europe1, there have been very few reports from India.2-5  It is suspected that FH may be far more prevalent in India than it appears.2 Although Triclabendazole is the drug of choice it is not available in India. Nitazoxanide has been reported to be effective in FH. Computed tomography (CT) has been reported to have characteristic features of FH. We present a case series of 16 patients, the largest so far from India to the best of our knowledge, diagnosing FH cases by characteristic CT findings against a background of typical clinical features and demonstrate its response to treatment with Nitazoxanide.


16 patients, from the year 2010 to 2016, presented to us with chronic pain in the right hypochondrium. Several had fever and significant weight loss. Blood investigations, chest xray, urine and stool examinations were ordered. All patients had ultrasound (USG) of the abdomen done elsewhere which showed indeterminate liver lesions. Hence a triphasic contrast enhanced 64 slice CT (Aquilion One, Canon, Tokyo, Japan) was performed with intravenous contrast of 1 to 1.5 ml/Kg of iopromide (Ultravist 370; Schering, Berlin, Germany) upto a maximum of 100 ml at a rate of 4 mL/s. Scans were obtained during the arterial, portal and hepatic venous phases with a section thickness of 0.5 mm. 9 patients had an ERCP with examination of the aspirated bile. As triclabendazole was not available to us, all our patients received Nitazoxanide for two weeks. 43% of the patients also received other drugs like Ivermectin, Praziquantel and Albendazole from their treating physicians. In 15 patients clinical follow up and in 9 patients post treatment imaging and AEC were available. 


Of the 16 cases, 7 were male and 9 female between 15 and 71 years of age. 15 were from northeastern India. All patients habitually consumed raw vegetables and leafy greens. All had pain in the right hypochondrium of half to several months duration. 31% reported significant weight loss and 56% had fever. All had significant eosinophilia with a mean AEC of 2305. Stool examinations revealed ova or parasites in none. In 4 cases adult worm or ova were detected in bile. Table 1 gives the details of the confirmed cases of FH and Tables 2A and 2B of the unconfirmed cases.

56% patients had abnormal liver function tests with elevation predominantly of the GGTP and serum alkaline phosphatase. ESR was raised in 33% and WBC count in 31%.
Typical CT features included hepatomegaly, grapelike clusters of cystic lesions 2 to 3 cm in diameter with uniform thickness moderately enhancing walls beginning at the liver periphery and radiating towards the hilum of the liver in the distribution of bile ducts, subcapsular fluid at the point of entry of parasite, mild dilatation of the proximal segmental ducts, inflammatory changes in the adjacent liver in the form of edema and increased enhancement, periportal reactive adenopathy, mild dilatation of the common bile duct (CBD) with diffuse mild wall thickening and lucent filling defects suggestive of parasite or sludge containing ova and meandering linear tunnel like hypodense channels in liver suggestive of  the parasite burrowing through liver tissue to reach biliary radicles. In one of our patients the meandering channels were also found in an enlarged spleen (Figures 1 and 2). We have named the cystic lesions “fasciola cluster of grapes sign” and the meandering linear lesions “fasciola tunnel sign”. Treatment in the unconfirmed cases was started based on the characteristic clinical and CT features.One patient had a segmental resection of the lesion, which showed dense eosinophilic infiltrates.
94% patients symptomatically improved remarkably. 100% patients who had post treatment repeat blood investigation showed resolution of eosinophilia.
100% patients who had post treatment imaging showed remarkable radiological regression of disease. 


Human fascioliasis is caused by the trematodes Fasciola hepatica and Fasciolagigantica.  It is reported worldwide.6 FH is a flat, leaf-shaped hermaphroditic parasite, and needs two hosts to complete its life cycle. The definitive hosts are herbivorous mammals. Humans are accidental hosts who acquire infection by consumption of contaminated raw vegetables or drinking water.6 Intermediate hosts are freshwater snails. Fasciola flukes live in the hepatic bile ducts of their definitive hosts and eggs pass out with the host’s feces. The eggs hatch into ciliated miracidia on contact with water and infect fresh water snails. Free cercaria leave the snail, attach to aquatic plants like watercress and develop into metacercarial cysts. Infection of the definitive host consists of two stages, the hepatic and the biliary stage. After ingestion, the metacercaria ex-cyst in the duodenum and migrate through the intestine wall into the peritoneum, and via the Glisson’s capsule into the liver. The larvae then migrate through the hepatic parenchyma. This hepatic phase lasts for 4 months and patient presents with fever, nausea, vomiting, urticaria, right hypochondriac pain, hepatomegaly, hypergamma-globulinaemia, anaemia and marked eosinophilia. All our patients had right hypochondriac pain and marked eosinophilia.
The chronic biliary stage occurs in the months following ingestion when adult flukes mature in the biliary tract and begin laying eggs. This can result in intermittent right hypochondriac pain, with or without cholangitis or cholestasis due to chronic bile duct inflammation. Eggs appear in the stool during this phase. Demonstrating the eggs in stool sample may need repeat samples with concentration procedures. Since we did not do this it may explain the negative stool exam in all our confirmed cases.  
Imaging can play a definitive role in the noninvasive diagnosis of FH. USG, which is the first investigation of choice, may show hypoechoic areas in the liver in the hepatic stage. However these are not specific to FH and may also be found in hepatic neoplasia. All our patients had indeterminate findings on USG. CT at this stage shows characteristic grape like clusters of cysts, which represent granulomas in the biliary distribution radiating from the liver capsule where the parasite enters to the central biliary tree. Oblique reformations are especially useful for demonstration of above findings. All our 16 patients had these typical findings proving the “fasciola cluster of grapes sign” on CT to be a reliable sign.To our knowledge, only FH can produce the “facsiola tunnel sign” which is another specific sign on CT making CT a definitive imaging tool for FH. A contrast enhanced MRI may show similar findings but is less easily available and less amenable to dynamic multiplanar reformations. A biopsy though considered definitive at this stage can be avoided if these characteristic features are picked up on meticulously performed and analysed CT. In the biliary stage gall bladder and CBD may show echogenic leaf like filling defects on USG, which when showing motility suggests adult live worms.7
One of the reasons for FH being reported less than its prevalence in India could be due to the non-availability of CT as well as inaccurate interpretation of the CT findings.8
Endoscopic retrograde cholangiopancreatico-graphy (ERCP) may demonstrate the adult worm within the CBD or gall bladder, can obtain ova in biliary and duodenal aspirate and aids in the management by sphincterotomy and removal of the adult worms.9
Triclobendazole10, a benzimidazole, is the current drug of choice. Unfortunately, the drug is not available for human use in India. Nitazoxanide, a thiazolide derivative is active against a variety of protozoa and has been studied for FH with reasonable success.11-14 Although, 43% of our patients had received albendazole, praziquantel and ivermectin empirically, these drugs have not been shown to have any effect on fasciola as per previous studies.6,15 In addition, all our patients that receivednitazoxanide alone showed remarkable clinical improvement as well. Those who had blood and imaging investigation showed resolution of eosinophilia and regression of disease. The good response to treatment in all our patients can therefore be attributed to nitazoxanide.
We acknowledge the limitation of our case series in that only four cases were proven on the basis of demonstration of the adult worm or larva. 


Human fascioliasis should be suspected in patients who present with right hypochondriac pain, significant weight loss, eosinophilia, fever, elevated serum alkaline phosphatase, GGTP, ESR and WBC count with characteristic imaging findings of the “fasciola cluster of grapes sign” and the “fasciola tunnel sign”on CT scan. ERCP is useful for retrieval of adult worms and ova as stool examinations are often negative. If triclabendazole is not available, nitazoxanide should be the drug of choice.

  1. Marcos LA, Terashima A, Gotuzzo E. Update on hepatobiliary flukes: Fascioliasis, opisthorchiasis and clonorchiasis. CurrOpin Infect Dis 2008;21:523-30.
  2. Ramachandran J, Ajjampur S, Chandramohan A, Varghese G M. Cases of human fascioliasis in India: Tip of the iceberg. J Postgrad Med 2012; 58:150-2.
  3. Elhence V, Mehta B, Gupta RK. Fascioliasis: A case from central Uttar Pradesh. Indian J Gastroenterol 2001; 20:164.
  4. Narain K, Biswas D, Rajguru SK, Mahanta J. Human distomatosis due to Fasciola hepatica infection in Assam, India. J Commun Dis 1997; 29:161-5.
  5. Madhumitha R, Gohel S, Vishwanathan L, Gopalakrishnan R. Liver Lesions, Fever and Eosinophilia Caused by Fasciola hepatica in a 15-year-old Girl. Indian J Pediatr. 2015 Oct;82(10):967-8. 
  6. WHO headquarters, Geneva, Switzerland 17–18 October 2006. Report of the WHO Informal Meeting on use of triclabendazole in fascioliasis control. Available online:
  7. Kabaalioglu A, Ceken K, Alimoglu E, Saba R, Cubuk M, Arslan G et al. Hepatobiliaryfascioliasis: sonographic and CT findings in 87 patients during the initial phase and long-term follow-up. American journal of roentgenology. 2007 Oct;189(4):824-8
  8. Nyindo M, Lukambagire AH. Fascioliasis: an ongoing zoonotic trematode infection. BioMed research international. 2015 Aug 31;2015.
  9. Gulsen MT, Savas MC, Koruk M, Kadayifci A, Demirci F. Fascioliasis: A report of five cases presenting with common bile duct obstruction. Neth J Med. 2006 Jan 1;64(1):17-9.
  10. Tolan RW. Fascioliasis due to Fasciola hepatica and Fasciolagigantica infection: an update on this ‘neglected’neglected tropical disease. Laboratory Medicine. 2011 Feb 1;42(2):107-16.
  11. Ortiz JJ, Ayoub A, Gargala G, Chegne NL, Favennec L. Randomized clinical study of nitazoxanide compared to metronidazole in the treatment of symptomatic giardiasis in children from Northern Peru. Alimentary pharmacology & therapeutics. 2001 Sep 27;15(9):1409-15.
  12. Kabil SM, Ashry EE, Ashraf NK. An open-label clinical study of nitazoxanide in the treatment of human fascioliasis. CurrTher Res 2000;61:339-45.
  13. Favennec L, Jave Ortiz J, Gargala G, Lopez Chegne N, Ayoub A, Rossignol JF. Double-blind, randomized, placebo-controlled study of nitazoxanide in the treatment of facioliasis in adults and children from northern Peru. Aliment PharmacolTher 2003;17:265-70.
  14. Rossignol JF, Abaza H, Friedman H. Successful treatment of human fascioliasis with nitazoxanide. Trans R Soc Trop Med Hyg 1998;92:103-4.
  15. Fang W, Chen F, Liu HK, Yang Q, Yang L. Comparison between albendazole and triclabendazole against Fasciolagigantica in human. Zhongguoxue xi chongbing fang zhizazhi= Chinese journal of schistosomiasis control. 2014 Feb;26(1):106-8.