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Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

67
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...
67

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Giant Obstructing Left Ventricular Dedifferentiated Liposarcoma.

Michele Dell'Aquila1, Joost Ter Woorst2, Ferdi Akca2

  • 1Department of Cardiothoracic Surgery, Catharina Ziekenhuis, Eindhoven, the Netherlands; Department of Cardiothoracic Surgery, Weill Cornell Medicine, New York, New York, USA.

JACC. Case Reports
|June 6, 2025
PubMed
Summary
This summary is machine-generated.

A 52-year-old woman experienced new-onset atrial fibrillation caused by an incidentally discovered intracardiac mass. Surgical removal of the left ventricular dedifferentiated liposarcoma and mitral valve replacement were successful, followed by adjuvant radiotherapy.

Keywords:
cardiac dedifferentiated liposarcomacardiac sarcomacardiac tumor

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Area of Science:

  • Cardiology
  • Oncology
  • Cardiac Surgery

Background:

  • Intracardiac masses can present with diverse clinical manifestations.
  • Atrial fibrillation is a common arrhythmia that can be secondary to various cardiac conditions.
  • Dedifferentiated liposarcoma is a rare malignant mesenchymal tumor, with intracardiac presentation being exceptionally uncommon.

Purpose of the Study:

  • To report a rare case of new-onset atrial fibrillation secondary to an intracardiac dedifferentiated liposarcoma.
  • To highlight the diagnostic and therapeutic challenges associated with intracardiac tumors.
  • To emphasize the importance of considering rare etiologies in the differential diagnosis of cardiac masses.

Main Methods:

  • Case presentation of a 52-year-old female patient.
  • Diagnostic workup including incidental finding of an intracardiac mass.
  • Surgical resection of the mass and mitral valve replacement.
  • Adjuvant radiotherapy as part of the treatment protocol.

Main Results:

  • Successful surgical excision of a paravalvular, obstructing, dedifferentiated liposarcoma located in the left ventricle.
  • Mitral valve replacement was performed concurrently with tumor resection.
  • The patient tolerated adjuvant radiotherapy.
  • Ongoing follow-up to monitor for recurrence or complications.

Conclusions:

  • Dedifferentiated liposarcoma can present as an intracardiac mass causing significant cardiac dysfunction, such as atrial fibrillation.
  • Multidisciplinary management involving cardiac surgery, oncology, and potentially radiation oncology is crucial for optimal outcomes.
  • Complete surgical resection followed by adjuvant therapy may be beneficial in managing this rare malignancy.