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Surgical Management of Cardiac Hydatid Cyst and the Residual Intramural Ectocyst
Firas F Ibrahim1, David Rubay2, Slee Yi3
1Cardiac Surgery, Iraqi Center of Heart Diseases, Baghdad, IRQ.
Insights
Cardiac hydatid cysts (HCs) are rare, often asymptomatic, and diagnosed via imaging. This case highlights a young male with coexisting hepatic and cardiac HCs, successfully treated with emergency surgery.
Area of Science:
- Cardiology
- Parasitology
- Infectious Diseases
Background:
- Hydatid cyst (HC) is a parasitic infection caused by Echinococcus tapeworms, endemic in livestock-raising regions.
- Cardiac hydatid cysts are exceptionally rare, often presenting with nonspecific symptoms, necessitating advanced imaging for diagnosis.
- Concurrent hydatid cysts in multiple organs, such as the liver and heart, require thorough investigation.
Observation:
- A young male presented with nonspecific symptoms, leading to the discovery of combined hepatic and cardiac hydatid cysts during diagnostic workup.
- The cardiac hydatid cyst was intramurally located within the interventricular septum, extending towards the diaphragmatic surface of the left ventricle and partially involving the right ventricle.
- The patient underwent emergency open-heart surgery for the removal of the cardiac hydatid cyst.
Findings:
- Surgical removal of the endocyst was performed, with drainage of the intramural ectocyst to mitigate risks of recurrence or residual space complications.
- Histopathological examination confirmed the diagnosis of hydatid cyst in both hepatic and cardiac locations.
- The patient experienced a favorable postoperative recovery, underscoring the feasibility of surgical intervention for cardiac hydatid cysts.
Implications:
- This case underscores the importance of a comprehensive diagnostic approach in patients with hydatid disease, considering potential multi-organ involvement.
- Early diagnosis and surgical management are crucial for favorable outcomes in cardiac hydatid cyst cases.
- Increased awareness among clinicians regarding the possibility of cardiac hydatid cysts, even in the absence of typical symptoms, is warranted.
Abstract:
The cardiac hydatid cyst (HC) is a rare pathology and mostly is endemic in livestock raising countries. Patients do not have a specific presentation so it is mainly a diagnosis based on imaging. Finding HC anywhere in the body warrants looking for another hydatid in other organs. This is a case report of a young male who presented with nonspecific symptoms and during diagnostic workup, it happened that he has combined hepatic and cardiac HCs. The cardiac cyst was located intramurally in the interventricular septum and expanding down mostly to the left side of the diaphragmatic surface of the heart and partly crossing intramurally to the diaphragmatic surface of the right ventricle. Emergency open-heart surgery was performed; the endocyst was removed while intramural ectocyst was drained to prevent potential future residual space.
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