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Transient Transduction of the Strobilated Forms of Echinococcus granulosus
Published on: September 16, 2022
Cardiac echinococcosis with negative serologies: a report of two cases
Mehrdad Salehi1, Aliakbar Soleimani
1Cardiac Surgery Ward, Imam Khomeini Hospital, Medical Sciences, University of Tehran, Iran.
Insights
Cardiac hydatid cysts are rare, especially after prior surgeries. Two cases highlight the need for vigilant monitoring to detect new Echinococcosis formations in the heart and other organs.
Area of Science:
- Medicine
- Parasitology
- Cardiology
Background:
- Hydatid cyst disease, caused by Echinococcus granulosus, rarely affects the heart (approx. 2% of cases).
- Serologic tests can be negative in some hydatid cyst cases, complicating diagnosis.
- Recurrence or new cyst formation can occur even after surgical removal of existing cysts.
Observation:
- Two cases of cardiac hydatid cysts are presented, both with initially negative serologic tests.
- Case 1: Liver hydatid cyst surgery followed by cardiac symptoms 10 years later.
- Case 2: Brain and breast hydatid cyst surgeries preceded cardiac cyst diagnosis 3 years later.
Findings:
- Transthoracic two-dimensional echocardiography was crucial for diagnosing cardiac hydatid cysts in both patients.
- Surgical excision and histological examination confirmed the diagnosis in both instances.
- These cases demonstrate rare instances of cardiac localization of hydatid cysts post-surgery.
Implications:
- Highlights the importance of considering hydatid disease in cardiac presentations, even with negative serology.
- Stresses the need for long-term, comprehensive patient follow-up after hydatid cyst surgery.
- Emphasizes vigilant re-evaluation for new hydatid cyst development in the heart and other sites due to Echinococcosis.
Abstract:
Cardiac involvement in hydatid cyst disease is uncommon, occurring in approximately 2% of hydatid cases. Two cases of cardiac hydatid cysts with negative serologic tests are reported herein. In Case 1, the patient underwent surgery to remove cysts from the liver and 10 years later presented with symptoms and signs of ischaemic heart disease. In Case 2, the patient first underwent surgery to remove cysts from the brain and 3 years later for cyst removal from the breast. In both cases the diagnosis was established by transthoracic two-dimensional echocardiography and then confirmed by surgery and histological examination. These cases are of particular interest because of the rarity of cardiac localisation as a new site of the hydatid cyst after one or more previous surgeries for hydatid cyst removal, and stress the need for frequent reevaluation to detect new hydatid cyst formation in the heart and elsewhere caused by the Echinococcosis organism.
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