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Related Concept Videos

Chronic Obstructive Pulmonary Disease II: Emphysema01:23

Chronic Obstructive Pulmonary Disease II: Emphysema

Emphysema, a major phenotype of chronic obstructive pulmonary disease (COPD), is characterized by irreversible destruction of alveolar walls and permanent enlargement of distal airspaces. Unlike chronic bronchitis, which primarily affects the airways, emphysema predominantly involves the lung parenchyma, where structural damage leads to airflow limitation.PathophysiologyIt most commonly results from prolonged exposure to cigarette smoke and other toxic gases, particularly cigarette smoke.
Pulmonary Tuberculosis II01:28

Pulmonary Tuberculosis II

Tuberculosis, or TB, is a bacterial infectious disease caused by Mycobacterium tuberculosis. While its primary impact is on the lungs, leading to pulmonary tuberculosis, it can also affect various other organs, a condition referred to as extrapulmonary tuberculosis.
Here is a detailed explanation of its pathophysiology:
Transmission: The process begins when a person inhales droplet nuclei containing M. tuberculosis. These are typically released into the air when an individual with pulmonary or...
Amebiasis01:28

Amebiasis

Entamoeba histolytica, a protozoan parasite, is responsible for intestinal and extraintestinal amebiasis. Though a significant proportion of infections remain asymptomatic, approximately 50 million individuals annually are estimated to present with clinical disease, resulting in up to 100,000 deaths globally. The disease burden is disproportionately high in regions with lower socioeconomic status, such as parts of India, Africa, Mexico, and Latin America.Etiology and TransmissionThe infective...
Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

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, but...
Pulmonary Edema II: Pathophysiology01:18

Pulmonary Edema II: Pathophysiology

Pulmonary edema is the accumulation of fluid in the interstitial and alveolar spaces of the lungs, impairing gas exchange and oxygen delivery. It may be cardiogenic or noncardiogenic, but both reduce oxygenation and lung compliance.Cardiogenic Pulmonary EdemaCardiogenic edema results from increased hydrostatic pressure in pulmonary capillaries, usually due to left ventricular dysfunction from myocardial infarction, heart failure, or valvular disease. Ineffective cardiac pumping causes blood to...
Pulmonary Embolism I: Introduction01:29

Pulmonary Embolism I: Introduction

Pulmonary embolism (PE) occurs when a thrombus, fat or air embolus, amniotic fluid, or tumor tissue blocks one or more pulmonary arteries. These blockages originate in the venous system or the right side of the heart.EtiologyPE primarily arises from deep vein thrombosis (DVT) and other hypercoagulable states, such as inherited thrombophilias. Additional etiological factors include venous stasis, commonly seen in obesity, and endothelial injury from surgery and trauma. Less common causes include...

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Updated: Jun 15, 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

Pulmonary cystic echinococcosis.

Saul Santivanez1, Hector H Garcia

  • 1Center for Global Health and Department of Microbiology, School of Sciences, Universidad Peruana Cayetano Heredia, Peru.

Current Opinion in Pulmonary Medicine
|March 11, 2010
PubMed
Summary

Pulmonary cystic echinococcosis, a parasitic lung infection, is often found incidentally and diagnosed via imaging. Surgery is the primary treatment, with chemotherapy as an alternative when surgery is not feasible.

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Published on: November 4, 2015

Area of Science:

  • Parasitology
  • Public Health
  • Infectious Diseases

Background:

  • Pulmonary cystic echinococcosis is a zoonotic disease caused by Echinococcus granulosus larvae.
  • It poses a significant public health challenge in regions with extensive livestock herding.
  • Existing literature is fragmented, necessitating a systematic overview.

Purpose of the Study:

  • To provide a comprehensive summary of pulmonary cystic echinococcosis.
  • To offer guidance for clinicians managing this condition.
  • To consolidate scarce and unsystematic literature.

Main Methods:

  • Systematic review of available literature.
  • Analysis of diagnostic imaging (radiographs, CT scans).
  • Evaluation of serological diagnostic support.

Main Results:

  • Lung involvement is more common in children than adults.
  • Pulmonary echinococcosis is often detected incidentally via imaging.
  • Symptoms arise from cyst mass effect; complications include rupture and secondary infection.
  • Diagnosis relies on imaging and serology.
  • Chemotherapy can reduce recurrence risk; benzimidazoles are an alternative to surgery.

Conclusions:

  • Imaging is the primary diagnostic tool for pulmonary cystic echinococcosis.
  • Surgical intervention remains the principal treatment modality.