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Cardiac hydatidosis mimicking ischemic heart disease: A case report
Andres Chaponan-Lavalle1, Cherie Quiroz Cortegana2, Luis Ivan Gordillo Velasquez2
1Universidad Peruana de Ciencias Aplicadas, Lima, Peru.
Insights
Cystic echinococcosis (CE) rarely affects the heart but poses challenges. Surgical removal and medication successfully treated a cardiac hydatid cyst in a Peruvian woman, highlighting the need for awareness in endemic areas.
Area of Science:
- Cardiology
- Parasitology
- Infectious Diseases
Background:
- Cystic echinococcosis (CE), caused by *Echinococcus granulosus*, is a zoonotic parasitic disease.
- Cardiac involvement in CE is rare (<2% of cases) but clinically significant and challenging to manage.
- Early diagnosis and treatment are crucial for favorable outcomes in cardiac CE.
Abstract:
Cystic echinococcosis (CE), caused by Echinococcus granulosus, is a zoonotic disease with cardiac involvement reported in less than 2 % of cases but associated with significant clinical challenges. We describe a 44-year-old woman from Peru who presented with exertional chest pain and T-wave inversions on electrocardiography. Imaging revealed a large multiloculated cystic mass with peripheral calcifications in the left ventricular wall, and Western Blot serology confirmed CE. The patient underwent surgical excision under cardiopulmonary bypass, followed by albendazole therapy. Histopathology confirmed a non-viable hydatid cyst. Postoperative recovery was uneventful, and she remained asymptomatic at 16-month follow-up. This case underscores the importance of considering cardiac hydatidosis in endemic regions when evaluating patients with angina-like symptoms in the presence of a cystic cardiac mass on imaging. Public awareness, improved medical education, and ongoing research are crucial to better managing this condition.
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