Canadian‐Acquired Hydatid Disease: A Case Report
Author(s) -
Mohammed Al Saghier,
Mark C. Taylor,
Howard M. Greenberg
Publication year - 2001
Publication title -
canadian journal of infectious diseases and medical microbiology
Language(s) - English
Resource type - Journals
eISSN - 1918-1493
pISSN - 1712-9532
DOI - 10.1155/2001/302738
Subject(s) - albendazole , medicine , jaundice , echinococcus , percutaneous , echinococcosis , surgery , portography , disease , general surgery , portal hypertension , pathology , gastroenterology , cirrhosis
Echinococcal cysts are unusual in Canada, and most cases seen are in immigrants. In northern Canadian communities, Echinococcus granulosis infection occasionally is acquired from dogs that feed on the entrails of caribou or moose. Seventeen patients with Canadian-acquired hydatid cysts were seen over an 11-year period. One challenging case is described in detail. An 18-year-old aboriginal woman presented with jaundice, pain, lower extremity edema and coagulopathy from a 26 cm echinococcal hepatic cyst. She was successfully treated with a combination of oral albendazole, percutaneous drainage and surgery. One-year follow-up showed no recurrence of disease. The management options for echinococcal cysts are extensively reviewed.
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