Evidence map›Paper›PMID 41069750›Full record

ArticleClinical case reports2025

Hepatic Fascioliasis Mimicking Hydatid Cyst and Complicated by Portal Vein Thrombosis: A Case Report From Ethiopia.

Binyam Mulatu Habte, Yoseph Mulatu Habte, Makida Mulatu Habte, Selamawit Gudeta Jima, Alazar Sitotaw, Mekoya Mengistu

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Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Binyam Mulatu HabteCollege of Medicine and Health Sciences University of Gondar Gondar Ethiopia.ORCID https://orcid.org/0009-0001-4489-3352
Yoseph Mulatu HabteEthio Tebib Hospital Addis Ababa Ethiopia.
Makida Mulatu HabteYekatit 12 Hospital Medical College Addis Ababa Ethiopia.
Selamawit Gudeta JimaYekatit 12 Hospital Medical College Addis Ababa Ethiopia.
Alazar SitotawDepartment of Internal Medicine Yekatit 12 Hospital Medical College Addis Ababa Ethiopia.ORCID https://orcid.org/0009-0009-8153-5018
Mekoya MengistuDepartment of Internal Medicine Yekatit 12 Hospital Medical College Addis Ababa Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fascioliasis is a zoonotic helminthic infection often underdiagnosed in humans, particularly in endemic regions like Ethiopia. In its hepatic migratory phase, it can mimic other liver pathologies such as hydatid cysts or pyogenic liver abscesses, making diagnosis difficult. We report a case of a 48-year-old Ethiopian woman with a three-month history of right upper quadrant abdominal pain, intermittent fever, and vomiting. She frequently consumed raw lettuce and tomatoes. Laboratory evaluation revealed leukocytosis with marked eosinophilia. Abdominal ultrasound showed a heterogeneous hepatic lesion, raising suspicion for hydatid cyst or early liver abscess. Triphasic CT revealed multiple confluent hypoattenuating lesions in segment VII and thrombosis of the right anterior portal vein. Although serologic, parasitologic, and histopathologic confirmation was unavailable, the diagnosis of hepatic fascioliasis was strongly supported by clinical findings, radiologic features, endemic exposure, and rapid response to triclabendazole. Anti-parasitic therapy and anticoagulation resulted in clinical and hematologic improvement. This case highlights the diagnostic challenges of hepatic fascioliasis in low-resource settings and the importance of considering it in patients with hepatic lesions, eosinophilia, and portal vein thrombosis. To our knowledge, this is the first reported Ethiopian case of hepatic fascioliasis complicated by portal venous thrombosis.

Indexed as

eosinophiliaEthiopiafascioliasishydatid cyst mimicliver abscessportal vein thrombosis

Identifiers

PMID41069750
PMCPMC12504130

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