Cardiac hydatid cyst: report of two cases

Haşim Ustünsoy1, Ilyas Akdemir, M Cumhur Sivrikoz

  • 1Department of Thoracic and Cardiovascular Surgery, Gaziantep University Medical Faculty, Gaziantep, Turkey. hustunsoy@yahoo.com

Heart, Lung & Circulation
|December 15, 2005
PubMed

Insights

Cardiac hydatid cysts are rare but life-threatening. Early diagnosis and surgical treatment, alongside albendazole therapy, are crucial for survival in patients with these cardiac masses.

Area of Science:

  • Medicine
  • Cardiology
  • Parasitology

Background:

  • Cardiac hydatid cyst is a rare but potentially fatal condition.
  • Often asymptomatic, it can lead to severe complications if not diagnosed early.
  • Prompt diagnosis and treatment are essential for patient survival.

Purpose of the Study:

  • To report two distinct cases of cardiac hydatid cysts.
  • To highlight diagnostic modalities and successful treatment strategies.
  • To emphasize the importance of early intervention for this rare cardiac pathology.

Main Methods:

  • Case report of two patients with cardiac hydatid cysts.
  • Diagnostic imaging included 2-D echocardiography and magnetic resonance imaging.
  • Surgical intervention utilized extracorporeal circulation with adjunctive albendazole therapy.

Main Results:

  • A 30-year-old woman presented with a large, primary multivesicular hydatid cyst in the left ventricle.
  • A 17-year-old woman had multivisceral involvement including a cardiac hydatid cyst with an atrial septal defect and pulmonary hypertension.
  • Both cases were successfully treated with surgical excision and albendazole.

Conclusions:

  • Cardiac hydatid cysts, though rare, require timely diagnosis and aggressive management.
  • Multimodality imaging is key for accurate diagnosis.
  • Surgical resection combined with medical therapy offers a life-saving treatment option.

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Mitral Stenosis II: Clinical features and Diagnostic Tests01:23

Mitral Stenosis II: Clinical features and Diagnostic Tests

Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...