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Updated: Aug 24, 2026

Transient Transduction of the Strobilated Forms of Echinococcus granulosus
Published on: September 16, 2022
[Cardiopericardial echinococcosis]
Abdallah Mahdhaoui1, Hatem Bouraoui, Mohamed Amine Majdoub
1Service de cardiologie Hôpital Farhat Hached 4000 Sousse, Tunisie. Abdallah.Mahdhaoui@famso.rnu.tn
Insights
Cardiac echinococcosis is rare, but transthoracic echocardiography (TTE) and transesophageal echocardiography (TEE) are effective for diagnosis. These imaging techniques aid in identifying cardiac hydatid cysts, even with atypical symptoms in endemic areas.
Area of Science:
- Cardiology
- Parasitology
- Medical Imaging
Context:
- Cardiac hydatid cysts are uncommon, accounting for 0.5-2% of human echinococcosis cases.
- This study reviews 12 patients diagnosed with cardiac echinococcosis between 1992 and 2001.
Purpose:
- To describe the clinical and echographic features of cardiac echinococcosis.
- To evaluate the diagnostic utility of various imaging modalities for cardiac hydatid cysts.
Summary:
- The study analyzed 12 patients (average age 40) with cardiac hydatid cysts located in the ventricles, atria, or pericardial cavity.
- Transthoracic echocardiography (TTE) and transesophageal echocardiography (TEE) were diagnostic in all cases, with CT and MRI providing additional information on disease extent.
- Surgical intervention was performed on all patients, resulting in one postoperative death and no late recurrences or complications.
Impact:
- Highlights the importance of considering cardiac echinococcosis in patients from endemic regions with unusual symptoms.
- Establishes TTE and TEE as primary imaging modalities for diagnosing cardiac hydatid cysts.
- Demonstrates the effectiveness of surgical treatment and the low recurrence rate for cardiac echinococcosis.
Unlabelled:
Cardiac hydatid cysts are rare and represent 0.5 to 2% off all hydatid cyst in human. We describe clinical and echographic features in 12 patients with cardiac echinococcosis, admitted between 1992 and 2001. Average age was 40 years (16-60 years). The cysts were located in the left ventricle wall (3 patients), right ventricle wall (3 patients) right atrium (3 patients) and pericardial cavity (3 patients). Cardiac Hydatid cyst diagnosis was established by transthoracic echocardiography (TTE) and transoesophageal echocardiography (TEE) in all cases. Computed tomography and magnetic resonance imaging confirmed echographic finding. All patients were operated. The operation finding confirmed the imaging data. Only one patient died in the post operative period. No recurrence or associated complication were reported in the late follow up.
Conclusion:
In presence of atypical symptomatology in a patient coming from an endemic area of hydatid cyst the diagnosis of cardiac echinococcosis is possible. TTE and TEE are the imaging procedure of choice and sufficient for the diagnosis of cardiac hydatid cyst. CT and/or MRI provide more information about the extension of echinococcosis diseases in other intra or extrathoracic location.
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