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Related Concept Videos

Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

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Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
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Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

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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...
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The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
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Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
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Related Experiment Video

Updated: Apr 25, 2026

Cell-based Therapy for Heart Failure in Rat: Double Thoracotomy for Myocardial Infarction and Epicardial Implantation of Cells and Biomatrix
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Multimodality treatment for cardiac angiosarcoma.

Meng Wang1, Ganglan Fu, Huiqi Jiang

  • 1Department of Cardiac Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, China.

Internal Medicine (Tokyo, Japan)
|September 2, 2014
PubMed
Summary
This summary is machine-generated.

Multimodality treatment, including chemotherapy, radiotherapy, and targeted therapy, offers hope for improving survival in patients with primary cardiac angiosarcoma, a rare and aggressive cancer. This approach demonstrated a 33-month survival in a case study.

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Area of Science:

  • Cardiovascular Pathology
  • Surgical Oncology
  • Medical Oncology

Background:

  • Primary cardiac angiosarcoma is a rare, highly malignant tumor with controversial adjuvant treatment strategies.
  • Complete surgical excision is the primary treatment, but its efficacy in improving survival is debated.

Observation:

  • A case of a 30-year-old male with right atrial angiosarcoma is presented.
  • The patient underwent two surgical resections and received chemotherapy, radiotherapy, and molecular targeted therapy for metastatic disease involving an intestinal segment.

Findings:

  • The patient achieved a survival of 33 months with multimodality treatment.
  • A review of existing literature, primarily case reports, on adjuvant therapy for cardiac angiosarcoma was conducted.

Implications:

  • Limited evidence suggests that multimodality treatment may improve survival outcomes for cardiac angiosarcoma patients.
  • Further research and larger studies are needed to establish definitive adjuvant treatment protocols for this rare malignancy.