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Hepatic schistosomiasis with massive splenomegaly: a case report and literature review

Journal Volume 81 - 2018
Issue Fasc.1 - Case reports
Author(s) L. Thijs, P. Messiaen, J. Van der Hilst, V. Madoe, C. Melis, P. Van Eyken, I. Vanmoerkerke, F. Janssens
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(1) Department of Gastroenterology and Hepatology, Jessa Ziekenhuis Hasselt, Belgium ; (2) Department of Infectious Diseases and Immunity, Jessa Ziekenhuis Hasselt, Belgium ; (3) BIOMED research institute, Hasselt University, Belgium ; (4) Department of Haematology, Jessa Ziekenhuis Hasselt, Belgium ; (5) Department of Pathological Anatomy, Ziekenhuis Oost-Limburg Genk, Belgium.

Schistosomiasis is a parasitic disease caused by Schistosoma species. Intestinal and hepatic schistosomiases are the most common forms of chronic disease. We describe a case of a 26-year old patient from Eritrea who was referred to our hospital with abdominal pain and diarrhea. The diagnosis of hepatosplenic schistosomiasis was made by liver biopsy and the patient was treated with praziquantel. Hepatic schistosomiasis is characterised by deposition of schistosomal eggs in the liver which results in a host cell immune response and leads to granuloma formation and neo- angiogenesis. This is hallmarked by different grades of periportal fibrosis with portal hypertension leading to splenomegaly. Normal liver architecture is preserved and periportal fibrosis can be reversible if treated adequately and timely. With a recent native schistosomiasis cluster report from France and the expected influx to Europe of persons from regions endemic for schistosomiasis, increased awareness of this disease in healthcare practitioners is needed. We review the epidemiology, pathogenesis, clinical presentation and treatment of schistosomiasis. (Acta gastroenterol. belg., 2018, 81, 93-96 Key words : Schistosoma, S. mansoni, hepatic fibrosis, splenomegaly

© Acta Gastro-Enterologica Belgica.
PMID 29562382