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Related Concept Videos

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,...
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...
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
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 V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

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...
Location and Orientation of the Heart01:13

Location and Orientation of the Heart

The human heart, despite its modest size and weight, is an organ of remarkable strength and endurance. Roughly the size of a fist, the heart weighs between 250 and 350 grams and is nestled within the mediastinum, the medial cavity of the thorax. It extends obliquely for about 12 to 14 cm, resting on the superior surface of the diaphragm. The heart is positioned anterior to the vertebral column and posterior to the sternum, with two-thirds of its mass lying to the left of the midsternal line.

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Minimal Invasive Resection of Large Retrosternal Thyroid Goiter
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Minimal Invasive Resection of Large Retrosternal Thyroid Goiter

Published on: September 20, 2024

Giant mediastinal thymolipoma simulating cardiomegaly.

Prasanna Simha Mohan Rao1, Nagaraja Moorthy, Ravindranath Khandenahalli Shankarappa

  • 1Department of Cardio-thoracic & Vascular Surgery, Sri Jayadeva Institute of Cardiology, Bangalore, India.

Journal of Cardiology
|September 29, 2009
PubMed
Summary

Thymolipomas, rare anterior mediastinal tumors, can mimic heart enlargement on chest X-rays. This case highlights their importance in diagnosing unexplained shortness of breath and enlarged cardiac silhouette.

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Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques
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Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques

Published on: June 11, 2019

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Minimal Invasive Resection of Large Retrosternal Thyroid Goiter
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Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques
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Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques

Published on: June 11, 2019

Area of Science:

  • Oncology
  • Thoracic Surgery
  • Diagnostic Imaging

Background:

  • Thymolipomas are rare anterior mediastinal tumors originating from thymic epithelial cells and adipose tissue.
  • These tumors can present insidiously, often discovered incidentally or when causing mass effect.
  • Differential diagnosis for anterior mediastinal masses includes thymoma, lymphoma, germ cell tumors, and thymolipoma.

Observation:

  • A middle-aged male presented with progressive dyspnea over two months.
  • Chest radiography revealed an enlarged cardiac silhouette, suggesting cardiomegaly.
  • Computed tomography (CT) demonstrated a large anterior mediastinal mass encasing the heart.

Findings:

  • Needle biopsy initially suggested lymphomatous material but was ultimately diagnosed as thymolipoma.
  • Surgical resection via median sternotomy achieved complete tumor removal (en bloc).
  • Histopathological examination confirmed the diagnosis of thymolipoma.

Implications:

  • This case underscores the necessity of including mediastinal tumors in the differential diagnosis for patients with dyspnea and apparent cardiomegaly.
  • Advanced imaging like CT is crucial for characterizing mediastinal masses and guiding diagnosis.
  • Early recognition and surgical management of thymolipoma can lead to favorable outcomes.