Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Aneurysm II: Clinical Manifestations and Diagnostic Studies01:21

Aneurysm II: Clinical Manifestations and Diagnostic Studies

124
Thoracic, aortic arch and abdominal aneurysms are significant vascular conditions that can present with various clinical manifestations and lead to serious complications. Understanding these manifestations and the appropriate diagnostic studies is essential for effective management and treatment.Thoracic Aortic AneurysmsThoracic aortic aneurysms often remain asymptomatic until they reach a size that impinges on adjacent structures. They typically cause deep, diffuse chest pain that radiates to...
124
Aneurysm III: Interprofessional Care01:26

Aneurysm III: Interprofessional Care

163
Aneurysm management involves either conservative medical therapy or surgical intervention, depending on the size and symptoms of the aneurysm. Conservative management is generally reserved for smaller, asymptomatic aneurysms, while larger or symptomatic aneurysms often necessitate surgical repair.Conservative Medical TherapyFor small, asymptomatic aneurysms, particularly abdominal aortic aneurysms (AAA) less than 5.5 centimeters in diameter, conservative medical therapy is recommended. This...
163
Aneurysm I: Introduction01:30

Aneurysm I: Introduction

195
An aortic aneurysm is a localized outpouching or dilation at a weak point in the artery wall. It may involve different parts of the aorta, such as the abdominal aorta, aortic arch, or thoracic aorta.Etiological factorsSeveral disorders are associated with aortic aneurysms.Congenital causes, such as primary connective tissue disorders like Marfan syndrome, impact the integrity and strength of connective tissues, notably affecting the aorta. Marfan syndrome is a genetic disorder that specifically...
195
Abdominal Aorta01:25

Abdominal Aorta

1.8K
Once the aorta traverses the diaphragmatic plane at the aortic hiatus, it is known as the abdominal aorta. This anatomical structure is positioned leftward of the spinal column, encased within a cocoon of adipose tissue behind the peritoneal cavity. It terminates at the L4 vertebra, where it splits into the common iliac arteries. Prior to this bifurcation, the abdominal aorta gives rise to several vital branches.
The celiac trunk, a singular artery, divides into the left gastric artery, which...
1.8K
Aortic Regurgitation II: Clinical Features and Diagnostic Tests01:22

Aortic Regurgitation II: Clinical Features and Diagnostic Tests

269
Aortic valve regurgitation (AR) occurs when the aortic valve fails to close properly, allowing blood to flow backward from the aorta into the left ventricle. This backflow can result in two distinct clinical presentations: acute and chronic AR, each characterized by its own set of symptoms and physical findings.Acute Aortic RegurgitationAcute AR presents with a sudden onset of severe symptoms. Patients typically experience profound dyspnea (shortness of breath), chest pain, and signs of left...
269
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

252
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...
252

You might also read

Related Articles

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

Sort by
Same author

Comparison of Cardiac MR with PET CT in Evaluation of Myocardial Viability: Single-Center Experience.

The Indian journal of radiology & imaging·2026
Same author

Reflected-wire technique for internal carotid artery catheterisation via the left radial approach in cerebral angiography.

Minimally invasive therapy & allied technologies : MITAT : official journal of the Society for Minimally Invasive Therapy·2026
Same author

Diagnostic performance of 68 Ga-DOTANOC PET/computed tomography in cardiac sarcoidosis: comparison with 18 F-fluorodeoxyglucose PET/computed tomography and cardiac magnetic resonance.

Nuclear medicine communications·2026
Same author

Comparison of Dual-Energy CT Derived Myocardial Delayed Enhancement with Magnetic Resonance Imaging in Patients with Cardiomyopathy-Related Heart Failure.

The Indian journal of radiology & imaging·2026
Same author

Imaging considerations in tetralogy of Fallot: A comprehensive review.

World journal of radiology·2026
Same author

Chikungunya infection complicated by encephalitis and rhabdomyolysis.

Tropical doctor·2025

Related Experiment Video

Updated: Dec 17, 2025

Modified Octopus Technique for Thoracoabdominal Aortic Aneurysm
04:56

Modified Octopus Technique for Thoracoabdominal Aortic Aneurysm

Published on: August 1, 2025

387

Abdominal Aortic Occlusion by Hydatid Cysts.

Uma Debi1, Vikas Bhatia1, M S Sandhu1

  • 1Department of Radiodiagnosis and Imaging, Postgraduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India.

Aorta (Stamford, Conn.)
|June 30, 2020
PubMed
Summary

Hydatid disease is a rare parasitic infection that can affect the abdominal aorta. This condition may lead to serious complications such as pseudoaneurysm formation and arterial occlusion. The disease can spread to the aorta through embolization from cardiac cysts or direct invasion. The study highlights the importance of diagnostic imaging in identifying these cysts. The authors emphasize the need for early detection and specialized treatment approaches. The findings suggest that aortic hydatid disease is rare but can be life-threatening. The study contributes to the understanding of how this condition presents and progresses.

Keywords:
aortic hydatid diseaseEchinococcus infectionvascular parasitic infestationabdominal aorta complications

Frequently Asked Questions

More Related Videos

Author Spotlight: Using Point-of-Care Ultrasound for Comprehensive Evaluation of the Abdominal Aorta
07:12

Author Spotlight: Using Point-of-Care Ultrasound for Comprehensive Evaluation of the Abdominal Aorta

Published on: September 8, 2023

3.9K
Novel and Innovative Hybrid Technique for Type A Aortic Dissection
06:26

Novel and Innovative Hybrid Technique for Type A Aortic Dissection

Published on: March 28, 2025

732

Related Experiment Videos

Last Updated: Dec 17, 2025

Modified Octopus Technique for Thoracoabdominal Aortic Aneurysm
04:56

Modified Octopus Technique for Thoracoabdominal Aortic Aneurysm

Published on: August 1, 2025

387
Author Spotlight: Using Point-of-Care Ultrasound for Comprehensive Evaluation of the Abdominal Aorta
07:12

Author Spotlight: Using Point-of-Care Ultrasound for Comprehensive Evaluation of the Abdominal Aorta

Published on: September 8, 2023

3.9K
Novel and Innovative Hybrid Technique for Type A Aortic Dissection
06:26

Novel and Innovative Hybrid Technique for Type A Aortic Dissection

Published on: March 28, 2025

732

Area of Science:

  • Parasitology
  • Vascular Surgery
  • Infectious Disease

Background:

Hydatid disease is a parasitic infestation caused by the larval stage of Echinococcus. It can affect various parts of the body, but aortic involvement is uncommon. The disease typically spreads through embolization from cardiac cysts or direct invasion. Aortic hydatid disease can lead to severe complications, including anaphylaxis and pseudoaneurysm formation. Prior research has shown that hydatid cysts are more commonly found in the liver and lungs. The rarity of aortic involvement has limited the understanding of its clinical presentation. No prior work had resolved the full extent of complications associated with abdominal aortic occlusion. This gap motivated further investigation into the mechanisms and outcomes of aortic hydatid disease. The need for better diagnostic and management strategies remains unmet.

Purpose Of The Study:

This study aimed to explore the clinical presentation and complications of abdominal aortic hydatid disease. The specific problem is the rarity and severity of aortic involvement by hydatid cysts. The motivation stems from the lack of comprehensive data on this condition. The authors sought to highlight the mechanisms of embolization and direct invasion. They also aimed to describe the potential complications, such as arterial occlusion. The study contributes to the understanding of how hydatid disease affects the aorta. No prior work had fully characterized the intravascular and intramural locations of these cysts. This work addresses a critical knowledge gap in parasitic vascular disease.

Main Methods:

The study reviewed clinical cases of hydatid disease involving the abdominal aorta. The researchers analyzed the mechanisms of cyst spread, including embolization from cardiac sources. They examined the anatomical locations of the cysts, distinguishing intravascular from intramural involvement. The study focused on identifying the clinical manifestations of aortic hydatid disease. Data collection included patient histories, diagnostic imaging, and surgical reports. The authors evaluated the frequency of complications such as pseudoaneurysm and embolism. They also considered the diagnostic challenges associated with this rare condition. The approach combined literature review and case analysis to synthesize current evidence.

Main Results:

The strongest finding is the association between cardiac hydatid cysts and aortic embolization. The study found that aortic hydatid disease can occur via embolization or direct invasion. Intravascular and intramural cyst locations were both identified in affected patients. The most common complications included pseudoaneurysm formation and arterial occlusion. Anaphylaxis was reported as a rare but severe outcome of aortic involvement. The study also noted that systemic embolism can occur from dislodged cyst fragments. Diagnostic imaging plays a crucial role in identifying these cysts. The results emphasize the need for early detection and specialized management strategies.

Conclusions:

The authors synthesize evidence that aortic hydatid disease is rare but can lead to life-threatening complications. They propose that embolization from cardiac cysts is a primary mechanism of aortic involvement. The study highlights the importance of distinguishing intravascular from intramural cyst locations. The findings suggest that diagnostic imaging is essential for identifying these cysts. The authors emphasize the need for multidisciplinary approaches in managing this condition. They propose that early detection improves patient outcomes. The study does not claim that aortic hydatid disease is a common condition. The implications are specific to the clinical management of rare parasitic vascular disease.

The main complications include pseudoaneurysm formation, arterial occlusion, anaphylaxis, and systemic embolism.

Hydatid cysts can reach the abdominal aorta via embolization from cardiac cysts or direct invasion.

Diagnostic imaging helps identify the location and extent of cyst involvement in the aorta.

Intravascular cysts are within the blood vessel, while intramural cysts are within the vessel wall.

Embolization from cardiac cysts is a primary mechanism for aortic involvement by hydatid disease.

The authors suggest that early detection and multidisciplinary management are essential for improving outcomes.