A 66-year-old man visited our hospital for the evaluation of bulging mucosa observed by endoscopy at a medical check-up. He had mild dyspepsia and abdominal discomfort, and a history of diabetes, hypertension, and coronary stent insertion due to previous myocardial infarction. He denied any history of travelling to the Middle East or contact with pets. Abdominal computed tomography and ultrasonography revealed an approximately 7 cm sized cystic lesion with wall enhancement (Fig. 1). Blood chemistry was as follows: white blood cells, 9,490/μL (eosinophil, 16.1%); hemoglobin, 12.9 g/dL; platelets, 284 × 103/μL; serum albumin, 4.45 g/dL; serum bilirubin, 0.82 mg/dL; serum aspartate aminotransferase, 26 IU/L; serum alanine aminotransferase, 53 IU/L; and eosinophilic count, 1,510/μL. Additional laboratory findings including stool protozoa, helminth ova, serum Paragonimus, and sparganum immunoglobulin G were all negative.
Cyst aspiration was planned for further analysis of the hepatic cystic lesion. Ultrasound guided percutaneous 18-gauge needle aspiration showed transparent cystic fluid with multiple white rice-granule sized pellets (Fig. 2A). Microscopic analysis confirmed those granules as cystic echinococcosis (CE) due to Echinococcus granulosus (Fig. 2B and 2C). We strongly recommended surgical resection of the cyst, but he refused and was subsequently lost to follow-up.
Human CE remains an endemic disease in developing countries, usually in regions of Central Asia, China, Russia, and the Middle East. Adult E. granulosus parasitizes the small intestine of dogs and eggs are excreted in feces. The ingested eggs hatch and penetrate the human small intestine and migrate to liver. However, the route of parasite infection was not clear in our case. Treatment options are surgery, chemotherapy with benzimidazole or percutaneous cyst aspiration.
The study was approved by the Institutional Review Board of Yeungnam University Medical Center (IRB No. YUMC 2018-12-034) and informed consent was waived by the IRB.
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