Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy

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...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by

Same author

Selective transport capacity for K<sup>+</sup> over Na<sup>+</sup> is linked to the expression levels of PtSOS1 in halophyte Puccinellia tenuiflora.

Functional plant biology : FPB·2020

Same author

A dual-gas sensor for simultaneous detection of methane and acetylene based on time-sharing scanning assisted wavelength modulation spectroscopy.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy·2020

Same author

Urinary activated leukocyte cell adhesion molecule as a novel biomarker of lupus nephritis histology.

Arthritis research & therapy·2020

Same author

An FGFR/AKT/SOX2 Signaling Axis Controls Pancreatic Cancer Stemness.

Frontiers in cell and developmental biology·2020

Same author

Surgical treatment of low-grade brain tumors associated with epilepsy.

International review of neurobiology·2020

Same author

miR-374b-5p is increased in deep vein thrombosis and negatively targets IL-10.

Journal of molecular and cellular cardiology·2020

Same journal

Errata: Dampened Reactive Hematopoiesis and Systemic Inflammatory Response Following Early Recurrent Myocardial Infarction in Mice.

International heart journal·2026

Same journal

Severe Coronary Vasospasm with Extensive Myocardial Necrosis and Refractory Ventricular Fibrillation.

International heart journal·2026

Same journal

Effective Transcatheter Mitral Valve Repair for Reverse Remodeling in Cancer Therapy-Related Cardiac Dysfunction.

International heart journal·2026

Same journal

TIF1β Promotes Myocardial Ischemia-Reperfusion Injury by Stabilizing TRAF6 through Mediating TRAF6 SUMOylation.

International heart journal·2026

Same journal

Finerenone Attenuates Myocardial Fibrosis and Pyroptosis in Rats with Myocardial Infarction.

International heart journal·2026

Same journal

Efficacy of Steroid Therapy in Preventing Adverse Clinical Outcomes in Patients with Fulminant Myocarditis Requiring Mechanical Circulatory Support.

International heart journal·2026

See all related articles

Search research articles

Related Experiment Video

Updated: Nov 12, 2025

The In ovo CAM-assay as a Xenograft Model for Sarcoma

The In ovo CAM-assay as a Xenograft Model for Sarcoma

Published on: July 17, 2013

Primary Cardiac Angiosarcoma.

Shiqi Guo^1,2, Qiang Guo³

¹Department of Critical Care Medicine, The First Affiliated Hospital of Soochow University.

International Heart Journal

|March 18, 2021

Summary

This summary is machine-generated.

This case study highlights primary cardiac angiosarcoma, a rare heart tumor often misdiagnosed. Early detection and surgical intervention are crucial for improving prognosis in this aggressive malignancy.

Keywords:

Cardiac tumor Echocardiography Pericardial effusion Pneumonia

More Related Videos

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma

Published on: April 12, 2019

A Syngeneic Orthotopic Osteosarcoma Sprague Dawley Rat Model with Amputation to Control Metastasis Rate

A Syngeneic Orthotopic Osteosarcoma Sprague Dawley Rat Model with Amputation to Control Metastasis Rate

Published on: May 3, 2021

Related Experiment Videos

Last Updated: Nov 12, 2025

The In ovo CAM-assay as a Xenograft Model for Sarcoma

The In ovo CAM-assay as a Xenograft Model for Sarcoma

Published on: July 17, 2013

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma

Published on: April 12, 2019

A Syngeneic Orthotopic Osteosarcoma Sprague Dawley Rat Model with Amputation to Control Metastasis Rate

A Syngeneic Orthotopic Osteosarcoma Sprague Dawley Rat Model with Amputation to Control Metastasis Rate

Published on: May 3, 2021

Area of Science:

Cardiology
Oncology
Pathology

Background:

Primary cardiac angiosarcoma is a rare and aggressive malignant neoplasm originating in the heart.
This condition poses diagnostic challenges due to its potential to mimic other cardiopulmonary diseases.

Observation:

A 34-year-old male patient was diagnosed with primary cardiac angiosarcoma one month post-admission.
The patient's initial presentation may have been complicated by misdiagnosis.

Findings:

Cardiac angiosarcoma exhibits high malignancy with a propensity for local infiltration and systemic metastasis.
Despite surgical efforts, advanced disease significantly impacts patient survival.

Implications:

Emphasizes the need for heightened clinical suspicion for cardiac angiosarcoma in atypical presentations.
Highlights the importance of timely diagnosis and aggressive treatment strategies for improving outcomes in rare cardiac tumors.