Related Experiment Video
Updated: Mar 6, 2026
13:25
Transient Transduction of the Strobilated Forms of Echinococcus granulosus
Published on: September 16, 2022
3.6K
Portal hydatid with secondary cavernomatosis
Mª Belén Rodríguez Sanz1, Mª Del Mar Roldán Cuena2, Carlos Alberto Blanco Álvarez3
1Servicio de Cirugía General y Aparato Digestivo, Complejo Asistencial Avila, España.
Revista Espanola De Enfermedades Digestivas
|March 4, 2017
Summary
Hydatid cysts, a zoonotic parasitic infection, can recur years after surgery. This case highlights a rare complication of portal vein hydatid cyst with secondary cavernomatosis, emphasizing the need for vigilant follow-up.
Area of Science:
- Parasitology
- Infectious Diseases
- Hepatology
Background:
- Hydatid cyst is a zoonotic parasitic infection with a significant link to animals, especially dogs.
- It is caused by Echinococcus tapeworms, leading to cyst formation in various organs.
- Hepatic hydatid cysts are common, but complications and recurrences require careful management.
Related Concept Videos
02:30Metastasis
6.7K
Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
6.7K
01:29Cardiomyopathy III: Hypertrophic Cardiomyopathy
588
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...
588