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

Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

1.0K
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
1.0K
Urologic Endoscopic Procedure: Cystoscopic Examination01:28

Urologic Endoscopic Procedure: Cystoscopic Examination

5.3K
Meaning of Cystoscopic Examination:Cystoscopy is an essential diagnostic tool in urology that is used to assess the structure and function of the genitourinary system. It provides a direct view of the urethra, bladder, and, in some cases, the ureteral openings. This procedure helps detect structural abnormalities, infections, cancers, and blockages in the urinary tract. There are two types of cystoscopy:Flexible cystoscopy is commonly performed in outpatient settings due to its less invasive...
5.3K
Cystic Fibrosis: Management01:24

Cystic Fibrosis: Management

620
Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
620

You might also read

Related Articles

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

Sort by
Same author

Implementation of Integrated Behavioural Health in Outpatient Cardiology Care for Patients with Injection Drug Use-Associated Infective Endocarditis.

CJC open·2026
Same author

Parasitic infections in solid organ transplant.

The American journal of the medical sciences·2026
Same author

Necrotizing Fasciitis in Northern Italy: Clinical Characteristics, Risk Factors, and Prognostic Value of the LRINEC Score-A Single-Center Retrospective Case Series.

Infectious disease reports·2026
Same author

Diagnostic uncertainties in older inpatients with suspected heart failure with preserved ejection fraction: a pilot cohort study.

Internal and emergency medicine·2026
Same author

Updates on Chromoblastomycosis: Evolving Insights in Clinical Management and Therapeutic Strategies.

Current fungal infection reports·2026
Same author

Association Between Symptoms of Anxiety and Depression and Blood Pressure Variability in Older Outpatients.

High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension·2026

Related Experiment Video

Updated: Mar 28, 2026

Transient Transduction of the Strobilated Forms of Echinococcus granulosus
13:25

Transient Transduction of the Strobilated Forms of Echinococcus granulosus

Published on: September 16, 2022

3.7K

Cystic Echinococcosis.

Nelson Iván Agudelo Higuita1, Enrico Brunetti2, Cindy McCloskey3

  • 1Division of Infectious Diseases, Oklahoma University Health Sciences Center, Oklahoma City, Oklahoma, USA nagudelo96@gmail.com.

Journal of Clinical Microbiology
|December 18, 2015
PubMed
Summary
This summary is machine-generated.

Cystic echinococcosis, caused by Echinococcus granulosus, is a neglected tropical disease affecting over 1 million people globally. This review covers its epidemiology, clinical signs, and diagnostic methods.

More Related Videos

Isolation And Dendritic Cell-Uptake of Small Extracellular Vesicles from Echinococcus granulosus
09:04

Isolation And Dendritic Cell-Uptake of Small Extracellular Vesicles from Echinococcus granulosus

Published on: March 28, 2025

842
Microscopic Cyst Resection for the Treatment of Patients Diagnosed with Epididymal Cyst
03:10

Microscopic Cyst Resection for the Treatment of Patients Diagnosed with Epididymal Cyst

Published on: March 31, 2023

13.5K

Related Experiment Videos

Last Updated: Mar 28, 2026

Transient Transduction of the Strobilated Forms of Echinococcus granulosus
13:25

Transient Transduction of the Strobilated Forms of Echinococcus granulosus

Published on: September 16, 2022

3.7K
Isolation And Dendritic Cell-Uptake of Small Extracellular Vesicles from Echinococcus granulosus
09:04

Isolation And Dendritic Cell-Uptake of Small Extracellular Vesicles from Echinococcus granulosus

Published on: March 28, 2025

842
Microscopic Cyst Resection for the Treatment of Patients Diagnosed with Epididymal Cyst
03:10

Microscopic Cyst Resection for the Treatment of Patients Diagnosed with Epididymal Cyst

Published on: March 31, 2023

13.5K

Area of Science:

  • Medical Parasitology
  • Infectious Diseases
  • Public Health

Background:

  • Echinococcosis is a significant neglected tropical disease (NTD) globally.
  • The Echinococcus granulosus species causes cystic echinococcosis (CE), also known as cystic hydatid disease.
  • CE impacts over 1 million individuals and incurs substantial annual healthcare costs exceeding $3 billion.

Purpose of the Study:

  • To provide a comprehensive overview of cystic echinococcosis.
  • To discuss the epidemiology and clinical presentation of CE.
  • To outline current diagnostic approaches for E. granulosus infections.

Main Methods:

  • Literature review of epidemiological data.
  • Summary of clinical manifestations reported in medical literature.
  • Analysis of diagnostic strategies for cystic hydatid disease.

Main Results:

  • Echinococcus granulosus is a major cause of human echinococcosis worldwide.
  • CE presents with diverse clinical symptoms depending on cyst location.
  • Diagnosis relies on imaging, serology, and sometimes histopathology.

Conclusions:

  • Cystic echinococcosis remains a critical global health concern requiring effective control strategies.
  • Understanding epidemiology and clinical features is vital for timely diagnosis and management.
  • Continued research into improved diagnostic tools is necessary for better patient outcomes.