Primary Hydatid Cysts in Rare Sites: A Series of Four Cases

Abstract

Hydatid disease is caused by the larval stage of the tapeworm Echinococcus granulosus. The definitive hosts include dogs and canines. Humans are accidental hosts and do not play a role in the biological cycle of the worm. The mode of infection is through ingesting food contaminated with dog feces containing gravid proglottids and free eggs, which hatch in the intestine and form larvae. The larvae then penetrate the intestinal wall, enter the bloodstream, and typically settle in the liver followed by the lungs. However, in rare instances, hydatid cysts can occur in various unusual sites throughout the body and even in a disseminated manner, leading to atypical clinical presentations and diagnostic challenges. Hereby, authors report a series of four cases (three males and one female) of hydatid cysts occurring at unusual sites, mainly the brain, kidney, spleen, and lung. The common age group among the observed cases was the second to fourth decade, showing a male predominance. In cases of splenic and renal hydatid cysts, patients presented with intermittent dull aching pain over the left and right flanks, respectively. In both cases, ultrasonography revealed the presence of multiple cysts in the spleen and kidney. In the case of cerebral hydatid cysts, the patient provided a history of short-term memory loss along with a few non specific symptoms, and Magnetic Resonance Imaging (MRI) revealed a hyperintense cystic lesion. In pulmonary hydatid cysts, the patient presented with symptoms of cough, dyspnoea, chest pain, and expectoration. X-ray examination supported the presence of the cyst. Surgery, preferably radical cystectomy, is considered for treatment, and the diagnosis is always confirmed by histopathology.

Keywords

• atypical presentation
• echinococcus granulosus
• histopathology
• radical cystectomy