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Cardiac hydatid cyst in the right ventricle: An unusual case at a rare site
Nouradden N Aljaber1, Sultan A Alshoabi2, Abdulaziz A Qurashi2
1Department of Cardiology, Faculty of Medicine, Sana'a University, Sana'a, Republic of Yemen.
Insights
This case report details an extremely rare cardiac hydatid cyst in a 23-year-old woman's right ventricle. Surgical removal confirmed Echinococcus granulosus, with the patient recovering well after treatment.
Area of Science:
- Parasitology
- Cardiology
- Radiology
Background:
- Hydatid disease, caused by Echinococcus granulosus, typically affects the liver and lungs.
- Cardiac involvement is exceptionally rare, posing diagnostic and therapeutic challenges.
- Medical imaging is crucial for diagnosing parasitic infections like hydatid disease.
Abstract:
Hydatid disease is a parasitic infection by the larval stage of the tapeworm Echinococcus granulosus. It affects liver, lungs and rarely other organs. Medical imaging provide the basis for diagnosis. This case report describes an extremely rare location of cardiac hydatid cyst in the right ventricle of the heart. We describe a 23-year-old woman who presented with shortness of breath and productive cough. Laboratory investigations showed marked eosinophilia and anemia. Chest radiography and abdominal ultrasonography were unremarkable. Cardiac computed tomography (CT) identified two well-defined fluid densities in the right ventricle without contrast enhancement. A transthoracic echocardiography (TTE) showed two cystic lesions in the right ventricular cavity that was attached to the interventricular septum. Hydatid cyst was the most likely diagnosis followed by the possibility of a congenital cardiac cyst. An open-heart surgery with cardiac cystectomy was performed. Post-operative analysis of the resected specimens showed multiple hydatid cysts with living scolices of Echinococcus granulosus. The patient recovered uneventfully and was discharged on oral albendazole.
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